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Martorell, F.J. García, D. Jiménez-Gallo, J.C. Pascual, J. Pereyra-Rodríguez, L. Salgado, E. Villarrasa" "autores" => array:7 [ 0 => array:2 [ "nombre" => "A." "apellidos" => "Martorell" ] 1 => array:2 [ "nombre" => "F.J." "apellidos" => "García" ] 2 => array:2 [ "nombre" => "D." "apellidos" => "Jiménez-Gallo" ] 3 => array:2 [ "nombre" => "J.C." "apellidos" => "Pascual" ] 4 => array:2 [ "nombre" => "J." "apellidos" => "Pereyra-Rodríguez" ] 5 => array:2 [ "nombre" => "L." "apellidos" => "Salgado" ] 6 => array:2 [ "nombre" => "E." "apellidos" => "Villarrasa" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S1578219015002449" "doi" => "10.1016/j.adengl.2015.09.009" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219015002449?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731015002902?idApp=UINPBA000044" "url" => "/00017310/0000010600000009/v1_201511040159/S0001731015002902/v1_201511040159/es/main.assets" ] ] "itemSiguiente" => array:19 [ "pii" => "S1578219015002450" "issn" => "15782190" "doi" => "10.1016/j.adengl.2015.09.010" "estado" => "S300" "fechaPublicacion" => "2015-11-01" "aid" => "1204" "copyright" => "Elsevier España, S.L.U. and AEDV" "documento" => "article" "crossmark" => 1 "subdocumento" => "ssu" "cita" => "Actas Dermosifiliogr. 2015;106:725-32" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 1203 "formatos" => array:3 [ "EPUB" => 58 "HTML" => 605 "PDF" => 540 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Review</span>" "titulo" => "Skin Stem Cells: At the Frontier Between the Laboratory and Clinical Practice. Part 1: Epidermal Stem Cells" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "725" "paginaFinal" => "732" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Células madre de la piel: en la frontera entre el laboratorio y la clínica. Parte <span class="elsevierStyleSmallCaps">I</span>: células madre epidérmicas" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 965 "Ancho" => 3090 "Tamanyo" => 233513 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Concept of lineage tracing.</p> <p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">The figure shows a schematic of the information obtained from lineage tracing experiments. The technique consists of introducing a reporter gene associated with the marker of the cells of interest (A), thereby obtaining a fluorescent signal in the subgroup of cells of interest. All daughter cells of the labelled cells also have a fluorescent signal (B), but the intensity of the signal will decrease as the cells continue to divide. Thus, on the one hand, we can identify cells descended from the initially labelled cells, and on the other, assess the rate of division (the cells that maintain an intense signal over time will be the quiescent cells that divide very slowly—the stem cells—whereas the cells that lose color intensity will be the compromised progenitor cells [C]).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "I. Pastushenko, L. Prieto-Torres, Y. Gilaberte, C. Blanpain" "autores" => array:4 [ 0 => array:2 [ "nombre" => "I." "apellidos" => "Pastushenko" ] 1 => array:2 [ "nombre" => "L." 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A, Clinical image of apparently insignificant nodular lesion. B, Ultrasound image showing a large underlying fluid collection. C, High inflammatory activity evidenced by Doppler ultrasound.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "A. Martorell, F.J. García-Martínez, D. Jiménez-Gallo, J.C. Pascual, J. Pereyra-Rodriguez, L. Salgado, E. Vilarrasa" "autores" => array:7 [ 0 => array:2 [ "nombre" => "A." "apellidos" => "Martorell" ] 1 => array:2 [ "nombre" => "F.J." "apellidos" => "García-Martínez" ] 2 => array:2 [ "nombre" => "D." "apellidos" => "Jiménez-Gallo" ] 3 => array:2 [ "nombre" => "J.C." "apellidos" => "Pascual" ] 4 => array:2 [ "nombre" => "J." "apellidos" => "Pereyra-Rodriguez" ] 5 => array:2 [ "nombre" => "L." "apellidos" => "Salgado" ] 6 => array:2 [ "nombre" => "E." 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Martorell, F.J. García, D. Jiménez-Gallo, J.C. Pascual, J. Pereyra-Rodríguez, L. Salgado, E. Vilarrasa" "autores" => array:7 [ 0 => array:4 [ "nombre" => "A." "apellidos" => "Martorell" "email" => array:1 [ 0 => "antmarto@hotmail.com" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "F.J." "apellidos" => "García" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 2 => array:3 [ "nombre" => "D." "apellidos" => "Jiménez-Gallo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] 3 => array:3 [ "nombre" => "J.C." "apellidos" => "Pascual" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">d</span>" "identificador" => "aff0020" ] ] ] 4 => array:3 [ "nombre" => "J." "apellidos" => "Pereyra-Rodríguez" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">e</span>" "identificador" => "aff0025" ] ] ] 5 => array:3 [ "nombre" => "L." "apellidos" => "Salgado" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">f</span>" "identificador" => "aff0030" ] ] ] 6 => array:3 [ "nombre" => "E." "apellidos" => "Vilarrasa" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">g</span>" "identificador" => "aff0035" ] ] ] ] "afiliaciones" => array:7 [ 0 => array:3 [ "entidad" => "Servicio de Dermatología, Hospital de Manises, Valencia, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Dermatología, Hospital Universitario del Sureste, Arganda del Rey, Madrid, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Unidad de Gestión Clínica de Dermatología, Hospital Universitario Puerta del Mar , Cádiz, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Hospital General de Alicante, Alicante, Spain" "etiqueta" => "d" "identificador" => "aff0020" ] 4 => array:3 [ "entidad" => "Hospital Virgen del Rocío, Sevilla, Spain" "etiqueta" => "e" "identificador" => "aff0025" ] 5 => array:3 [ "entidad" => "Complejo Hospitalario de Pontevedra, Pontevedra, Spain" "etiqueta" => "f" "identificador" => "aff0030" ] 6 => array:3 [ "entidad" => "Hospital de Santa Creu i Sant Pau, Barcelona, Spain" "etiqueta" => "g" "identificador" => "aff0035" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Actualización en hidradenitis supurativa (<span class="elsevierStyleSmallCaps">ii</span>): aspectos terapéuticos" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 3923 "Ancho" => 3257 "Tamanyo" => 812875 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Treatment algorithm for hidradenitis suppurativa.</p> <p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Source: Martorell.<a class="elsevierStyleCrossRef" href="#bib0450"><span class="elsevierStyleSup">45</span></a></p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Hidradenitis suppurativa (HS) is currently considered an inflammatory disease of the pilosebaceous follicle with an underlying immune system imbalance that affects genetically predisposed individuals. The course of disease can be modified by exogenous triggers or aggravating factors.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1,2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The association between HS and autoimmune and autoinflammatory diseases, such as pyoderma gangrenosum and Crohn disease (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>),<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> together with clinical and laboratory findings, supports the existence of an immune system imbalance and consequently suggests inadequate control of the inflammatory response around hair follicles in intertriginous areas.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">HS represents a true therapeutic challenge, with dermatologists responsible for taking decisions regarding patients’ treatment needs.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">General Measures</span><p id="par0020" class="elsevierStylePara elsevierViewall">Numerous general measures can be taken to reduce situations that trigger flares, including tobacco cessation, weight reduction, control of cardiovascular risk factors, avoidance of the use of irritants in affected areas, and hair removal using lasers rather than razors.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> These measures should be complemented by adequate psychological support, which in some cases will need to be intensified.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Local Treatment</span><p id="par0025" class="elsevierStylePara elsevierViewall">The main noninvasive local treatment for localized Hurley stage I or mild stage II lesions is topical clindamycin 0.1% applied every 12<span class="elsevierStyleHsp" style=""></span>hours.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1–3</span></a> In one clinical trial, oral tetracycline administered at 500<span class="elsevierStyleHsp" style=""></span>mg/12<span class="elsevierStyleHsp" style=""></span>h did not show superior results to topical treatment with clindamycin.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">4</span></a> Topical resorcinol 15% has also proven to be effective in reducing the pain and duration of inflammatory lesions in patients with Hurley stage I or II lesions.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1–3</span></a> Intralesional corticosteroids are the most common invasive local treatment and the most widely used drug is slow-release triamcinolone acetonide (depot preparation 40<span class="elsevierStyleHsp" style=""></span>mg/mL). Triamcinolone acetonide injections result in the remission of inflammatory nodules within 48 to 72<span class="elsevierStyleHsp" style=""></span>hours in patients with acute local lesions.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">First-Line Systemic/Biologic Therapies</span><p id="par0030" class="elsevierStylePara elsevierViewall">First-line treatments for HS are treatments supported by high levels of evidence and favorable results.</p><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Systemic Treatments</span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Combined Treatment With Oral Clindamycin and Oral Rifampicin</span><p id="par0035" class="elsevierStylePara elsevierViewall">The combined use of clindamycin 300<span class="elsevierStyleHsp" style=""></span>mg/12<span class="elsevierStyleHsp" style=""></span>h and rifampicin 300<span class="elsevierStyleHsp" style=""></span>mg/12<span class="elsevierStyleHsp" style=""></span>h for 10 weeks is one of the most common treatments used to induce remission in patients with HS, regardless of disease severity (Hurley stage I, II, or III).<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> The beneficial effects of this combination of antibiotics have been confirmed by all series published to date, including a report of 116 patients.<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">5,6</span></a> The therapeutic effect is attributable to the anti-inflammatory properties of the 2 drugs and probably also to their ability to destroy the biofilm mentioned in the first part of this review article. The combination is well tolerated, as the most common adverse effects are gastrointestinal discomfort and diarrhea (generally mild).<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Other antibiotics used to treat HS are doxycycline, minocycline, and rifampicin associated with moxifloxacin and/or metronidazole, with variable response.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1–3</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Oral Acitretin</span><p id="par0045" class="elsevierStylePara elsevierViewall">The use of acitretin in the treatment of HS is justified by the involvement of psoriasiform hyperplasia in the etiology and pathogenesis of the disease. In a recent study (2014), Matusiak et al.<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">7</span></a> reported on the efficacy of acitretin (mean [SD] dose, 0.56 [0.08] mg/kg/d) in 17 patients with HS. Nine of the patients completed the 9 months of treatment, and 8 (47%) achieved a reduction of 50% from baseline in the Hidradenitis Suppurativa Severity Index. The authors concluded that acitretin appears to be a promising option for the management of HS, although they cautioned that its use might be limited by the high doses required.</p><p id="par0050" class="elsevierStylePara elsevierViewall">Isotretinoin has not proven to be effective in HS, probably because it primarily causes atrophy of hypertrophic sebaceous glands, which are seen in juvenile acne, but not in HS.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1,7</span></a></p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Dapsone</span><p id="par0055" class="elsevierStylePara elsevierViewall">Dapsone is a nonteratogenic sulfone antibiotic that has antibacterial and anti-inflammatory (mainly antineutrophilic) properties. In a study of 24 patients with Hurley stage I and II disease, treatment with dapsone at doses of between 50 and 200<span class="elsevierStyleHsp" style=""></span>mg/d resulted in significant clinical improvement in 38% of patients.<a class="elsevierStyleCrossRefs" href="#bib0265"><span class="elsevierStyleSup">8,9</span></a></p></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Biological Therapies</span><p id="par0060" class="elsevierStylePara elsevierViewall">According to the available evidence, the most effective tumor necrosis factor α (TNF-α) blockers in HS are adalimumab and infliximab.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">10</span></a></p><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Adalimumab</span><p id="par0065" class="elsevierStylePara elsevierViewall">Adalimumab is supported by the highest levels of evidence (including data from randomized clinical trials) and is considered the most specific treatment for HS.<a class="elsevierStyleCrossRefs" href="#bib0275"><span class="elsevierStyleSup">10–12</span></a> Based on the data available, it is currently the main drug for the treatment of refractory Hurley stage II disease or moderate to severe Hurley stage III disease.</p><p id="par0070" class="elsevierStylePara elsevierViewall">Dermatologists are familiar with the use of biologic therapy in the setting of cutaneous and articular psoriasis. The standard doses of adalimumab in these cases are 80<span class="elsevierStyleHsp" style=""></span>mg at week 0, 40<span class="elsevierStyleHsp" style=""></span>mg at week 1, and 40<span class="elsevierStyleHsp" style=""></span>mg every other week thereafter. There are, however, clear differences between psoriasis and HS, mainly related to the level of inflammatory activity (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). In the setting of TNF-α-dependent inflammatory disorders, gastroenterologists use adalimumab administered at doses that are twice as high as those used in psoriasis to treat inflammatory bowel disease (IBD), and Crohn disease in particular, as this has a higher inflammatory burden. The standard regimen used in this setting is 160<span class="elsevierStyleHsp" style=""></span>mg at week 0 and 80<span class="elsevierStyleHsp" style=""></span>mg at week 2, followed by 40<span class="elsevierStyleHsp" style=""></span>mg administered every week or every 2 weeks, as appropriate. According to the latest data available, HS appears to be closer to the inflammatory spectrum of IBD than of psoriasis, and therefore requires treatment with higher doses of adalimumab than those typically used in dermatology; the response rates would be expected to be similar to those seen in IBD.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0075" class="elsevierStylePara elsevierViewall">Results from the latest trials of adalimumab and HS have shown that, just as in IBD, higher induction and maintenance doses than those used in psoriasis are needed to achieve better disease control; the proposed regimen is 160<span class="elsevierStyleHsp" style=""></span>mg at week 0, 80<span class="elsevierStyleHsp" style=""></span>mg at week 2, and 40<span class="elsevierStyleHsp" style=""></span>mg a week from week 4 onwards.<a class="elsevierStyleCrossRefs" href="#bib0285"><span class="elsevierStyleSup">12–15</span></a> These higher doses are justified by the higher levels of TNF-α found in lesional skin in HS compared with psoriasis (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>).<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">16</span></a></p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0080" class="elsevierStylePara elsevierViewall">Reports on treatment efficacy for HS are also more similar to those published for IBD than for psoriasis. A retrospective Spanish study of the use of biologic therapy in HS reported complete, lasting remission in approximately 15% of patients and partial remission in approximately 50%.<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">14</span></a> These data, however, should be interpreted with caution as most patients were administered lower doses than those recommended for HS and IBD.</p><p id="par0085" class="elsevierStylePara elsevierViewall">In a double-blind, randomized, placebo-controlled trial of 154 patients with moderate to severe HS who did not respond to or tolerate tetracycline antibiotics, clinical response was achieved by week 16 in 17.6% of patients treated with adalimumab 40<span class="elsevierStyleHsp" style=""></span>mg weekly, 9.6% of patients treated with adalimumab 40<span class="elsevierStyleHsp" style=""></span>mg every 2 weeks (psoriasis regimen), and 3.9% of patients treated with placebo.<a class="elsevierStyleCrossRef" href="#bib0285"><span class="elsevierStyleSup">12</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">In a more recent phase 3 randomized, placebo-controlled trial (PIONEER II) involving 326 patients, patients were treated with an induction dose of 160<span class="elsevierStyleHsp" style=""></span>mg (week 0), followed by 80<span class="elsevierStyleHsp" style=""></span>mg at week 2, and 40<span class="elsevierStyleHsp" style=""></span>mg weekly starting at week 4. Response was evaluated using the Hidradenitis Suppurativa Clinical Response (HiSCR) measure, which is defined as a reduction of 50% or more in the count of inflammatory lesions (abscesses and inflammatory nodules) and no increase in abscesses or draining fistulas. At week 12, adalimumab proved to be significantly superior to placebo for the primary endpoint (HiSCR), with a satisfactory response observed in 50% of patients treated with this biologic. Efficacy was observed at week 2, and the adverse effects were similar to those seen in the placebo group and consistent with the safety profile of adalimumab.</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Infliximab</span><p id="par0095" class="elsevierStylePara elsevierViewall">Infliximab is the biologic with the longest tradition in the treatment of HS and its use is supported by high levels of evidence, second only to adalimumab.<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">17</span></a> As occurs with adalimumab, the best results are achieved with an intensified regimen of 5<span class="elsevierStyleHsp" style=""></span>mg/kg per month<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">17</span></a> (5<span class="elsevierStyleHsp" style=""></span>mg/kg at weeks 0, 2, and 6, and monthly thereafter). The main disadvantage of infliximab compared with adalimumab is the need to use an intensified regimen, as a majority of patients with HS are overweight or obese. Furthermore, infliximab infusions need to be administered at a day hospital. Formation of antidrug antibodies may be responsible for the reduction in efficacy observed in certain patients with HS treated with infliximab, but levels have not yet been analyzed in this setting.</p></span></span></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Second-Line Systemic/Biologic Therapies</span><p id="par0100" class="elsevierStylePara elsevierViewall">Treatments supported by a lower level of evidence or associated with less favorable results are considered second-line treatments for HS.</p><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Systemic Therapy</span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Hormone Therapy</span><p id="par0105" class="elsevierStylePara elsevierViewall">There have been isolated case reports of HS responding to contraceptive drugs, such as cyproterone, and antiandrogens, such as finasteride.<a class="elsevierStyleCrossRefs" href="#bib0255"><span class="elsevierStyleSup">6,18</span></a> Randhawa et al.<a class="elsevierStyleCrossRef" href="#bib0320"><span class="elsevierStyleSup">19</span></a> published a report on 3 pediatric patients with HS who responded favorably to finasteride.</p><p id="par0110" class="elsevierStylePara elsevierViewall">In a report on possible medical treatments in 350 patients with HS, Scheinfeld<a class="elsevierStyleCrossRef" href="#bib0315"><span class="elsevierStyleSup">18</span></a> considered that it would be interesting to investigate the use of dutasteride 0.5<span class="elsevierStyleHsp" style=""></span>mg/d, as it is a more potent blocker of 5α reductase isoenzyme than finasteride, and in addition, it blocks the type 1 isoenzyme, unlike finasteride.<a class="elsevierStyleCrossRefs" href="#bib0255"><span class="elsevierStyleSup">6,18</span></a> There are, however, no publications on its use in HS.</p></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Systemic Corticosteroids</span><p id="par0115" class="elsevierStylePara elsevierViewall">Patients with HS, like patients with other inflammatory diseases, experience clinical improvement with systemic corticosteroids. Treatment, however, is limited to short cycles due to the risk of long-term adverse effects. There are no standardized regimens for the use of systemic corticosteroids in HS.<a class="elsevierStyleCrossRefs" href="#bib0255"><span class="elsevierStyleSup">6,18</span></a></p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Ciclosporin</span><p id="par0120" class="elsevierStylePara elsevierViewall">Ciclosporin, a calcineurin inhibitor, is a potent immunosuppressant that is very active in inflammatory skin diseases. Its targets include T lymphocytes, interleukin (IL) 2, and TNF-α. Contrasting with the situation in psoriasis, only a few isolated reports showing the efficacy of ciclosporin in severe HS have been published.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> The potential of this immunosuppressant in HS should be studied in clinical trial settings.</p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Methotrexate</span><p id="par0125" class="elsevierStylePara elsevierViewall">Methotrexate has been described as an ineffective drug when used in isolation in HS,<a class="elsevierStyleCrossRef" href="#bib0325"><span class="elsevierStyleSup">20</span></a> but it has not been widely studied. It is frequently used in association with TNF-α blockers, and this combination is therefore supported by robust safety data. It would be interesting to evaluate its synergic effect with adalimumab and its potential for lengthening the therapeutic effect of this drug, as it does in psoriasis.</p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Alitretinoin</span><p id="par0130" class="elsevierStylePara elsevierViewall">Alitretinoin is a retinoid whose therapeutic potential in HS should be investigated for numerous reasons: it has lower teratogenic potential than acitretin due to its shorter half-life and is therefore suitable for use in women of childbearing age. It also has greater immunomodulatory effects due to its rexinoid effect. While it is not cheap, it is not more expensive than biologics, and finally, it is not an immunosuppressant.</p><p id="par0135" class="elsevierStylePara elsevierViewall">In an Italian study of 14 patients with HS, alitretinoin administered at 10<span class="elsevierStyleHsp" style=""></span>mg/d for 24 weeks resulted in clinical improvement in 78.5% of patients.<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">21</span></a> It would also be interesting to investigate response rates for the 30-mg/d dose.</p></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Other Treatments</span><p id="par0140" class="elsevierStylePara elsevierViewall">Alternative treatments supported by lower levels of evidence for HS include metformin 500<span class="elsevierStyleHsp" style=""></span>mg/8<span class="elsevierStyleHsp" style=""></span>h,<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> sulfasalazine 1<span class="elsevierStyleHsp" style=""></span>g/12<span class="elsevierStyleHsp" style=""></span>h,<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> and tacrolimus.<a class="elsevierStyleCrossRef" href="#bib0335"><span class="elsevierStyleSup">22</span></a></p></span></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Biologic Therapies</span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Anakinra/Canakinumab</span><p id="par0145" class="elsevierStylePara elsevierViewall">Anakinra is an IL-1 receptor antagonist. Although it is indicated for use in rheumatoid arthritis, it is now largely used as an orphan drug for the treatment of autoinflammatory diseases. IL-1 is a proinflammatory cytokine that is very closely associated with sterile inflammation and neutrophils,<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1,23</span></a> and hence neutropenia features among the drug's possible adverse effects. Response to anakinra has been reported in isolated cases of HS and in an open-label study of 6 patients.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> However, there have also been reports of treatment failures,<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> possibly due to the high levels of IL-1 detected in HS lesions, i.e., the drug may lack the ability to elicit a response in certain patients (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>). Anakinra is normally administered subcutaneously at a dose of 100<span class="elsevierStyleHsp" style=""></span>mg/d, but there has been a report of a patient responding to a dose of 200<span class="elsevierStyleHsp" style=""></span>mg/d.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> Local reactions are the main problem associated with the use of anakinra, although these tend to improve after 4 weeks of treatment. Anakinra should not be used in association with TNF-α blockers.</p><p id="par0150" class="elsevierStylePara elsevierViewall">Canakinumab is a fully human IgGκ monoclonal antibody targeting IL-1β. It selectively binds to IL-1β with high affinity, neutralizing its biological activity by blocking interaction with IL-1 receptors and preventing the production of inflammatory mediators. It is indicated in autoinflammatory syndromes, systemic juvenile idiopathic arthritis, and arthritic gout. It has an advantage over anakinra is that it is administered subcutaneously every 4 or 8 weeks. There has been a report of satisfactory response to canakinumab in a patient with HS and pyoderma gangrenosum.<a class="elsevierStyleCrossRef" href="#bib0340"><span class="elsevierStyleSup">23</span></a> However, its high cost is a deterrent for the conduct of larger studies in HS.</p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Ustekinumab</span><p id="par0155" class="elsevierStylePara elsevierViewall">Ustekinumab is a biologic that targets the p40 subunit of IL-12/IL-23. It has proven effective in the treatment of isolated cases of HS.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">1</span></a> Like adalimumab and infliximab, it is probably more effective when administered at an intensified regimen consisting of 90-mg doses every 2 months; this is supported by a report of treatment failure when administered at the lower dose used for psoriasis.<a class="elsevierStyleCrossRef" href="#bib0350"><span class="elsevierStyleSup">25</span></a></p></span></span></span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Surgical Treatment</span><p id="par0160" class="elsevierStylePara elsevierViewall">Surgery is indicated for the treatment of nodules and isolated fistulas and for severe, extensive disease that does not respond to medical treatment.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1,26,27</span></a> Its effectiveness, however, has not yet been evaluated in clinical trials.<a class="elsevierStyleCrossRef" href="#bib0360"><span class="elsevierStyleSup">27</span></a> Additionally, while the literature shows that surgery appears to achieve good results in milder forms of HS, high recurrence rates have been observed in patients with moderate or severe disease and high levels of cutaneous and systemic inflammation treated with surgery only.</p><p id="par0230" class="elsevierStylePara elsevierViewall">Several surgical techniques are indicated for HS:<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">1.</span><p id="par0235" class="elsevierStylePara elsevierViewall">Incision and drainage</p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">2.</span><p id="par0240" class="elsevierStylePara elsevierViewall">Unroofing and marsupialization</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">3.</span><p id="par0245" class="elsevierStylePara elsevierViewall">Localized excision</p></li><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">4.</span><p id="par0250" class="elsevierStylePara elsevierViewall">Wide excision</p></li></ul></p><p id="par0165" class="elsevierStylePara elsevierViewall">The choice of surgery and size of margins are determined by the area affected and the degree of involvement.</p><p id="par0170" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Preoperative care</span>. Prior reduction of inflammation is recommended in patients with high degrees of inflammation and unclear margins. A 10-to-12-week course of antibiotics is probably sufficient for mild and moderate cases, but a short cycle of oral corticosteroids can also be added. Patients with severe disease can be administered prednisone 40-60<span class="elsevierStyleHsp" style=""></span>mg/d for 2 to 3 days followed by a decreasing dose over an additional 10 to 12 days. Ciclosporin has also been used, as have TNF-α blockers. General hygiene and dietary measures are recommended in all cases.</p><span id="sec0120" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Incision and Drainage</span><p id="par0175" class="elsevierStylePara elsevierViewall">Incision with drainage is a simple technique that can be performed under local anesthesia on an outpatient basis. It tends to result in rapid relief of pain in the case of isolated nodules, but recurrence is common.<a class="elsevierStyleCrossRefs" href="#bib0365"><span class="elsevierStyleSup">28,29</span></a></p><p id="par0180" class="elsevierStylePara elsevierViewall">Punch debridement has also been proposed as a modification of this technique.<a class="elsevierStyleCrossRef" href="#bib0375"><span class="elsevierStyleSup">30</span></a> This procedure involves centering a biopsy punch with a diameter of 5 to 7<span class="elsevierStyleHsp" style=""></span>mm over an inflamed pilosebaceous unit, which is then debrided by digital pressure followed by curettage. The goal is to remove the remains of the sebaceous gland and/or the follicle containing cells involved in the generation of fistulas and fibrous tracts. Preliminary data suggest that recurrences are relatively infrequent with this technique.</p></span><span id="sec0125" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Unroofing</span><p id="par0185" class="elsevierStylePara elsevierViewall">Unroofing (or deroofing) with marsupialization is a simple technique that can also be performed on an outpatient basis.<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">31</span></a> In this technique, the fistulous tract or roof of a nodule is transfixed using a probe or a mosquito forceps; the tissue is then removed with the aid of a scissors, electric scalpel, or radiofrequency ablation, thereby exposing the bed of the lesion, which is scraped with a curette. The lesions are left to heal by secondary intention. Unroofing is suitable for recurrent painful stage I or II lesions, and results in acceptable cosmetic results. Approximately 17% of lesions treated using this technique have been found to recur within a mean of 4 to 6 months.<a class="elsevierStyleCrossRefs" href="#bib0380"><span class="elsevierStyleSup">31,32</span></a></p></span><span id="sec0130" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Local Excision</span><p id="par0190" class="elsevierStylePara elsevierViewall">Local excision has the same advantages and disadvantages as incision and drainage.</p></span><span id="sec0135" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Wide Excision</span><p id="par0195" class="elsevierStylePara elsevierViewall">Wide excision involves removing an entire affected area with margins extending beyond the visibly affected region. When used in combination with medical measures and treatments, wide excision is the technique that is most likely to achieve disease control in patients with chronic, extensive stage III disease.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">1–29</span></a> The surgical defect can be reconstructed using simple local or free flaps, skin grafts, tissue expanders, or simply closure by secondary intention.<a class="elsevierStyleCrossRef" href="#bib0390"><span class="elsevierStyleSup">33</span></a> Assuming that adequate margins can be guaranteed, the reconstruction method does not influence recurrence rates and should therefore be chosen according to the site of excision and the size of the lesion.<a class="elsevierStyleCrossRefs" href="#bib0395"><span class="elsevierStyleSup">34,35</span></a> Margins of between 0.5<span class="elsevierStyleHsp" style=""></span>cm (axillae) and 1.5<span class="elsevierStyleHsp" style=""></span>cm are recommended. Deep excision extending as far as the fascia or at least 5<span class="elsevierStyleHsp" style=""></span>mm of fat is important to ensure removal of the deep coils of the apocrine glands. Wide excision, however, does not protect against recurrence at distant apocrine sites.</p><p id="par0200" class="elsevierStylePara elsevierViewall">Several authors advise against using primary closure techniques due to the high risk of recurrence (54%-69.9% vs 13% for grafts and 18% for local flaps), but these higher rates are attributable to the higher number of affected margins or to incomplete resection.<a class="elsevierStyleCrossRef" href="#bib0355"><span class="elsevierStyleSup">26</span></a> Nonetheless, significant differences have been reported for recurrence rates associated with different reconstruction techniques, but it is difficult to compare modalities due to the nature of HS and the number of techniques that exist. Some studies that have assessed recurrence rates by location have reported lower rates in the axillae (3%) and perianal area (0%) than in the groin and perineal region (37%) and submammary area (50%), suggesting that recurrence is more common at sites with larger areas of apocrine glands.<a class="elsevierStyleCrossRef" href="#bib0355"><span class="elsevierStyleSup">26</span></a></p><p id="par0205" class="elsevierStylePara elsevierViewall">Vacuum-assisted closure involves the use of a device that delivers negative pressure to the wound and therefore promotes blood flow, increases the rate of granulation tissue formation, and facilitates wound drainage, thereby reducing bacterial load. This technique has been found to produce better results and lower rates of recurrence when used in larger wounds.<a class="elsevierStyleCrossRef" href="#bib0405"><span class="elsevierStyleSup">36</span></a></p></span></span><span id="sec0140" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0160">Lasers and Light</span><p id="par0210" class="elsevierStylePara elsevierViewall">A range of laser and light systems have been used in HS, with varying results. Carbon dioxide laser therapy results in improvement by clinically vaporizing all the layers of tissue as far as the deep subcutaneous fat or fascia. Recurrence is low.<a class="elsevierStyleCrossRef" href="#bib0410"><span class="elsevierStyleSup">37</span></a> Hair removal lasers and intense-pulsed light systems also result in clinical improvement by reducing the number of hair follicles and associated inflammation.<a class="elsevierStyleCrossRef" href="#bib0415"><span class="elsevierStyleSup">38</span></a> Long-pulsed (1064<span class="elsevierStyleHsp" style=""></span>nm) Nd:YAG 1064 laser therapy has also been described as effective for the treatment of Hurley stage II and III disease.<a class="elsevierStyleCrossRef" href="#bib0420"><span class="elsevierStyleSup">39</span></a> Finally, reports describing the use of photodynamic therapy in series of patients with HS have increased,<a class="elsevierStyleCrossRefs" href="#bib0425"><span class="elsevierStyleSup">40–42</span></a> but the results are varied and recurrence is high. A standardized photodynamic treatment regimen has not been described.</p></span><span id="sec0145" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0165">Other Treatments</span><p id="par0215" class="elsevierStylePara elsevierViewall">Radiation therapy is no longer used to treat HS due to the risk of tumors and the existence of alternative treatments.<a class="elsevierStyleCrossRef" href="#bib0440"><span class="elsevierStyleSup">43</span></a> However, classic studies of this technique show complete remission in 38% of cases and improvement in 40%. Cryotherapy has proven effective in the management of isolated cases of painful HS nodules, as has cryoinsufflation, which involves applying liquid nitrogen into small fistulous tracts using a needle that follows the path of the fistula, followed by 2 freeze cycles in the entire area.<a class="elsevierStyleCrossRefs" href="#bib0440"><span class="elsevierStyleSup">43,44</span></a> Unfortunately, recovery time is long and the treatment is quite painful.</p></span><span id="sec0150" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0170">Conclusions: Towards a Treatment Algorithm</span><p id="par0220" class="elsevierStylePara elsevierViewall">Our review of the different treatment options for HS shows that <span class="elsevierStyleItalic">a</span>) HS is a chronic skin disease with a significant systemic component (largely in moderate and severe forms of the disease) that needs to be controlled medically; <span class="elsevierStyleItalic">b</span>) HS is an inflammatory disease that needs to be treated with a combination of topical and systemic/biologic treatments and, occasionally, surgery of varying levels of complexity; and <span class="elsevierStyleItalic">c</span>) HS is a disabling disease whose management can be optimized by designing personalized therapies overseen by dermatologists with the involvement of primary care physicians, surgeons, and nursing staff, and occasional collaboration from other specialists, such as psychologists and gastroenterologists, among others (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>).<a class="elsevierStyleCrossRef" href="#bib0450"><span class="elsevierStyleSup">45</span></a> Recent data regarding the efficacy of adalimumab in HS, combined with the recent approval of this drug by the European Medicines Agency as a primary specific treatment for HS, will help us to manage cases that require maintenance therapy to achieve optimal control of inflammation.</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0155" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0175">Conflicts of Interest</span><p id="par0225" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:15 [ 0 => array:3 [ "identificador" => "xres576308" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec592961" "titulo" => "Keywords" ] 2 => array:3 [ "identificador" => "xres576307" "titulo" => "Resumen" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0010" ] ] ] 3 => array:2 [ "identificador" => "xpalclavsec592962" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "General Measures" ] 6 => array:2 [ "identificador" => "sec0015" "titulo" => "Local Treatment" ] 7 => array:3 [ "identificador" => "sec0020" "titulo" => "First-Line Systemic/Biologic Therapies" "secciones" => array:2 [ 0 => array:3 [ "identificador" => "sec0025" "titulo" => "Systemic Treatments" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0030" "titulo" => "Combined Treatment With Oral Clindamycin and Oral Rifampicin" ] 1 => array:2 [ "identificador" => "sec0035" "titulo" => "Oral Acitretin" ] 2 => array:2 [ "identificador" => "sec0040" "titulo" => "Dapsone" ] ] ] 1 => array:3 [ "identificador" => "sec0045" "titulo" => "Biological Therapies" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0050" "titulo" => "Adalimumab" ] 1 => array:2 [ "identificador" => "sec0055" "titulo" => "Infliximab" ] ] ] ] ] 8 => array:3 [ "identificador" => "sec0060" "titulo" => "Second-Line Systemic/Biologic Therapies" "secciones" => array:2 [ 0 => array:3 [ "identificador" => "sec0065" "titulo" => "Systemic Therapy" "secciones" => array:6 [ 0 => array:2 [ "identificador" => "sec0070" "titulo" => "Hormone Therapy" ] 1 => array:2 [ "identificador" => "sec0075" "titulo" => "Systemic Corticosteroids" ] 2 => array:2 [ "identificador" => "sec0080" "titulo" => "Ciclosporin" ] 3 => array:2 [ "identificador" => "sec0085" "titulo" => "Methotrexate" ] 4 => array:2 [ "identificador" => "sec0090" "titulo" => "Alitretinoin" ] 5 => array:2 [ "identificador" => "sec0095" "titulo" => "Other Treatments" ] ] ] 1 => array:3 [ "identificador" => "sec0100" "titulo" => "Biologic Therapies" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0105" "titulo" => "Anakinra/Canakinumab" ] 1 => array:2 [ "identificador" => "sec0110" "titulo" => "Ustekinumab" ] ] ] ] ] 9 => array:3 [ "identificador" => "sec0115" "titulo" => "Surgical Treatment" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "sec0120" "titulo" => "Incision and Drainage" ] 1 => array:2 [ "identificador" => "sec0125" "titulo" => "Unroofing" ] 2 => array:2 [ "identificador" => "sec0130" "titulo" => "Local Excision" ] 3 => array:2 [ "identificador" => "sec0135" "titulo" => "Wide Excision" ] ] ] 10 => array:2 [ "identificador" => "sec0140" "titulo" => "Lasers and Light" ] 11 => array:2 [ "identificador" => "sec0145" "titulo" => "Other Treatments" ] 12 => array:2 [ "identificador" => "sec0150" "titulo" => "Conclusions: Towards a Treatment Algorithm" ] 13 => array:2 [ "identificador" => "sec0155" "titulo" => "Conflicts of Interest" ] 14 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2015-05-04" "fechaAceptado" => "2015-06-30" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec592961" "palabras" => array:6 [ 0 => "Hidradenitis suppurativa" 1 => "Acne inversa" 2 => "Surgery" 3 => "Biologic therapy" 4 => "Systemic treatment" 5 => "Adalimumab" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec592962" "palabras" => array:6 [ 0 => "Hidradenitis supurativa" 1 => "Acné inversa" 2 => "Cirugía" 3 => "Terapia biológica" 4 => "Terapia sistémica" 5 => "Adalimumab" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Although hidradenitis suppurativa is a common and serious skin condition, its treatment is not well established. It is now accepted that the moderate and severe forms of the disease are associated with marked systemic inflammation. The goal of treatment in hidradenitis suppurative is therefore to achieve systemic control of inflammation. In some cases, surgery may also be necessary to reduce the severity of the manifestations of cutaneous inflammation. Recent advances in our understanding of hidradenitis suppurativa have been accompanied by the emergence of novel approaches to its treatment, including the use of certain biologic drugs. Several clinical trials have been undertaken to test the effects of biologics (mainly adalimumab) in this setting. In this review, we analyze the different treatments available for hidradenitis suppurativa.</p></span>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">A pesar de la importancia y de la gravedad de la hidradenitis supurativa, el tratamiento de esta enfermedad no se encuentra bien definido. Hoy en día, la hidradenitis es considerada una enfermedad cutánea que principalmente en las formas moderadas y severas se asocia a un marcado componente inflamatorio sistémico. Por lo tanto, el tratamiento de esta enfermedad irá enfocado hacia un manejo sistémico del control de la inflamación, que ocasionalmente irá acompañado de la intervención quirúrgica para reducir la carga de inflamación localizada en la piel.</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Los recientes avances en el conocimiento de la enfermedad se han acompañado de novedades terapéuticas, especialmente representadas por el desarrollo de ensayos clínicos de determinadas terapias biológicas, principalmente adalimumab, orientados al tratamiento específico de esta enfermedad.</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">En la presente revisión se pretende analizar las diferentes alternativas terapéuticas existentes en el manejo de la hidradenitis supurativa.</p></span>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Martorell A, García FJ, Jiménez-Gallo D, Pascual JC, Pereyra-Rodríguez J, Salgado L, et al. Actualización en hidradenitis supurativa (<span class="elsevierStyleSmallCaps">ii</span>): aspectos terapéuticos. Actas Dermosifiliogr. 2015;106:716–724.</p>" ] ] "multimedia" => array:4 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1979 "Ancho" => 3181 "Tamanyo" => 452554 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Immunology, clinical presentation, and therapeutic targets of neutrophilic autoinflammatory diseases. IL indicates interleukin; T<span class="elsevierStyleInf">H</span>17, type 17 helper T cells; TNF, tumor necrosis factor; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 507 "Ancho" => 1673 "Tamanyo" => 86242 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Comparative levels of proinflammatory cytokines (in number of times increased) in the skin of patients with hidradenitis suppurativa compared with psoriasis.</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 3923 "Ancho" => 3257 "Tamanyo" => 812875 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Treatment algorithm for hidradenitis suppurativa.</p> <p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Source: Martorell.<a class="elsevierStyleCrossRef" href="#bib0450"><span class="elsevierStyleSup">45</span></a></p>" ] ] 3 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Cutaneous psoriasis \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Hidradenitis suppurativa \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Less inflammation and easier to control \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Greater inflammation and more difficult to control \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Does not hurt but can cause itching \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Painful and oozes pus (bad smell and stains clothes) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Not disabling (except for psoriatic arthritis) and does not cause scarring \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Disabling and leaves permanent scars \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Less impact on quality of life \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Greater impact on quality of life \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Cannot degenerate into cancer \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Cancer can arise (chronic inflammation) in HS lesions, predominantly in the perianal and gluteal region \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Classic and biologic therapies (with summary of product characteristics and supported by studies with higher levels of evidence) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Adalimumab, only treatment with recommended approval from the European Medicines Agency following completion of randomized clinical trials \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab940623.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Differences Between Cutaneous Psoriasis and Hidradenitis Suppurativa That Influence Treatment of the Latter.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:45 [ 0 => array:3 [ "identificador" => "bib0230" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Comorbidities of hidradenitis suppurativa (acne inversa)" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "S. 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Year/Month | Html | Total | |
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2024 November | 9 | 9 | 18 |
2024 October | 129 | 49 | 178 |
2024 September | 125 | 44 | 169 |
2024 August | 182 | 75 | 257 |
2024 July | 156 | 35 | 191 |
2024 June | 177 | 53 | 230 |
2024 May | 213 | 56 | 269 |
2024 April | 167 | 29 | 196 |
2024 March | 199 | 46 | 245 |
2024 February | 182 | 47 | 229 |
2024 January | 182 | 60 | 242 |
2023 December | 174 | 46 | 220 |
2023 November | 173 | 69 | 242 |
2023 October | 146 | 48 | 194 |
2023 September | 156 | 35 | 191 |
2023 August | 147 | 31 | 178 |
2023 July | 134 | 66 | 200 |
2023 June | 114 | 47 | 161 |
2023 May | 132 | 64 | 196 |
2023 April | 112 | 35 | 147 |
2023 March | 122 | 45 | 167 |
2023 February | 118 | 32 | 150 |
2023 January | 107 | 40 | 147 |
2022 December | 95 | 36 | 131 |
2022 November | 78 | 47 | 125 |
2022 October | 39 | 34 | 73 |
2022 September | 38 | 58 | 96 |
2022 August | 42 | 41 | 83 |
2022 July | 43 | 46 | 89 |
2022 June | 44 | 42 | 86 |
2022 May | 92 | 58 | 150 |
2022 April | 119 | 70 | 189 |
2022 March | 119 | 94 | 213 |
2022 February | 89 | 82 | 171 |
2022 January | 81 | 57 | 138 |
2021 December | 90 | 60 | 150 |
2021 November | 79 | 62 | 141 |
2021 October | 87 | 58 | 145 |
2021 September | 77 | 53 | 130 |
2021 August | 71 | 32 | 103 |
2021 July | 67 | 38 | 105 |
2021 June | 67 | 33 | 100 |
2021 May | 65 | 32 | 97 |
2021 April | 132 | 44 | 176 |
2021 March | 90 | 30 | 120 |
2021 February | 87 | 32 | 119 |
2021 January | 58 | 26 | 84 |
2020 December | 55 | 31 | 86 |
2020 November | 55 | 28 | 83 |
2020 October | 56 | 12 | 68 |
2020 September | 81 | 25 | 106 |
2020 August | 55 | 28 | 83 |
2020 July | 57 | 29 | 86 |
2020 June | 56 | 30 | 86 |
2020 May | 54 | 28 | 82 |
2020 April | 57 | 24 | 81 |
2020 March | 47 | 30 | 77 |
2020 February | 8 | 5 | 13 |
2020 January | 4 | 6 | 10 |
2019 December | 9 | 4 | 13 |
2019 November | 4 | 5 | 9 |
2019 October | 0 | 5 | 5 |
2019 September | 8 | 2 | 10 |
2019 August | 4 | 1 | 5 |
2019 July | 5 | 9 | 14 |
2019 June | 12 | 21 | 33 |
2019 May | 3 | 101 | 104 |
2019 April | 1 | 52 | 53 |
2019 March | 8 | 10 | 18 |
2019 February | 0 | 12 | 12 |
2019 January | 2 | 6 | 8 |
2018 December | 2 | 2 | 4 |
2018 November | 1 | 2 | 3 |
2018 October | 2 | 2 | 4 |
2018 September | 5 | 9 | 14 |
2018 August | 0 | 22 | 22 |
2018 July | 0 | 6 | 6 |
2018 June | 0 | 7 | 7 |
2018 May | 0 | 12 | 12 |
2018 April | 0 | 9 | 9 |
2018 March | 2 | 6 | 8 |
2018 February | 47 | 13 | 60 |
2018 January | 55 | 12 | 67 |
2017 December | 51 | 22 | 73 |
2017 November | 52 | 21 | 73 |
2017 October | 56 | 17 | 73 |
2017 September | 42 | 19 | 61 |
2017 August | 40 | 36 | 76 |
2017 July | 24 | 35 | 59 |
2017 June | 40 | 42 | 82 |
2017 May | 28 | 24 | 52 |
2017 April | 28 | 26 | 54 |
2017 March | 31 | 24 | 55 |
2017 February | 28 | 17 | 45 |
2017 January | 31 | 16 | 47 |
2016 December | 35 | 26 | 61 |
2016 November | 50 | 46 | 96 |
2016 October | 35 | 27 | 62 |
2016 September | 2 | 7 | 9 |
2016 August | 0 | 5 | 5 |
2016 July | 1 | 10 | 11 |
2016 June | 1 | 21 | 22 |
2016 May | 0 | 14 | 14 |
2016 April | 0 | 31 | 31 |
2016 March | 0 | 16 | 16 |
2016 February | 0 | 24 | 24 |
2016 January | 0 | 44 | 44 |
2015 November | 0 | 85 | 85 |