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array:25 [ "pii" => "S0001731022008754" "issn" => "00017310" "doi" => "10.1016/j.ad.2022.10.021" "estado" => "S300" "fechaPublicacion" => "2022-12-01" "aid" => "3243" "copyright" => "AEDV" "copyrightAnyo" => "2021" "documento" => "simple-article" "crossmark" => 1 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "crp" "cita" => "Actas Dermosifiliogr. 2022;113 Supl 1:TS26-TS28" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "itemSiguiente" => array:19 [ "pii" => "S0001731021002969" "issn" => "00017310" "doi" => "10.1016/j.ad.2021.07.004" "estado" => "S300" "fechaPublicacion" => "2022-12-01" "aid" => "2729" "copyright" => "AEDV" "documento" => "simple-article" "crossmark" => 1 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "crp" "cita" => "Actas Dermosifiliogr. 2022;113 Supl 1:S29-S31" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "es" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">CARTA CIENTÍFICO-CLÍNICA</span>" "titulo" => "Úlceras de Lipschütz tras la vacuna frente a la COVID-19 de AstraZeneca" "tienePdf" => "es" "tieneTextoCompleto" => "es" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "S29" "paginaFinal" => "S31" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Lipschütz Ulcers after the AstraZeneca COVID-19 Vaccine" ] ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figura 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1205 "Ancho" => 905 "Tamanyo" => 186155 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Úlceras de Lipschütz. Lesiones redondeadas de bordes bien definidos y fondo grisáceo. Junto a introito vaginal, la de mayor tamaño (1,5<span class="elsevierStyleHsp" style=""></span>cm).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "N. González-Romero, V. Morillo Montañes, I. Vicente Sánchez, M. García García" "autores" => array:4 [ 0 => array:2 [ "nombre" => "N." "apellidos" => "González-Romero" ] 1 => array:2 [ "nombre" => "V." "apellidos" => "Morillo Montañes" ] 2 => array:2 [ "nombre" => "I." "apellidos" => "Vicente Sánchez" ] 3 => array:2 [ "nombre" => "M." "apellidos" => "García García" ] ] ] ] ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731021002969?idApp=UINPBA000044" "url" => "/00017310/00000113000000S1/v1_202212200523/S0001731021002969/v1_202212200523/es/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S0001731021003185" "issn" => "00017310" "doi" => "10.1016/j.ad.2021.07.007" "estado" => "S300" "fechaPublicacion" => "2022-12-01" "aid" => "2751" "copyright" => "AEDV" "documento" => "simple-article" "crossmark" => 1 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "crp" "cita" => "Actas Dermosifiliogr. 2022;113 Supl 1:S26-S28" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "es" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Carta científico-clínica</span>" "titulo" => "Sífilis secundaria granulomatosa: presentación de un caso sospechado a partir de los hallazgos histológicos" "tienePdf" => "es" "tieneTextoCompleto" => "es" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "S26" "paginaFinal" => "S28" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Granulomatous Secondary Syphilis Suggested by Histology: A Case Report" ] ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figura 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1066 "Ancho" => 1500 "Tamanyo" => 517234 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">A)<span class="elsevierStyleHsp" style=""></span>Tinción con hematoxilina-eosina (H-E) 40×. B)<span class="elsevierStyleHsp" style=""></span>H-E 200×. C)<span class="elsevierStyleHsp" style=""></span>H-E 400×.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "A. Fernández Camporro, J.M. Calzada González, P. Arcos González, E. Rodríguez Díaz" "autores" => array:4 [ 0 => array:2 [ "nombre" => "A." "apellidos" => "Fernández Camporro" ] 1 => array:2 [ "nombre" => "J.M." "apellidos" => "Calzada González" ] 2 => array:2 [ "nombre" => "P." "apellidos" => "Arcos González" ] 3 => array:2 [ "nombre" => "E." 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B)<span class="elsevierStyleHsp" style=""></span>H-E 200×. C)<span class="elsevierStyleHsp" style=""></span>H-E 400×.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "A. Fernández Camporro, J.M. Calzada González, P. Arcos González, E. Rodríguez Díaz" "autores" => array:4 [ 0 => array:2 [ "nombre" => "A." "apellidos" => "Fernández Camporro" ] 1 => array:2 [ "nombre" => "J.M." "apellidos" => "Calzada González" ] 2 => array:2 [ "nombre" => "P." "apellidos" => "Arcos González" ] 3 => array:2 [ "nombre" => "E." "apellidos" => "Rodríguez Díaz" ] ] ] ] ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731021003185?idApp=UINPBA000044" "url" => "/00017310/00000113000000S1/v1_202212200523/S0001731021003185/v1_202212200523/es/main.assets" ] ] "en" => array:15 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Case and Research Letter</span>" "titulo" => " Granulomatous Secondary Syphilis Suggested by Histology: A Case Report" "tieneTextoCompleto" => true "saludo" => "<span class="elsevierStyleItalic">To the Editor</span>," "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "TS26" "paginaFinal" => "TS28" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Á. Fernández Camporro, J.M. Calzada González, P. Arcos González, E. Rodríguez Díaz" "autores" => array:4 [ 0 => array:4 [ "nombre" => "Á." "apellidos" => "Fernández Camporro" "email" => array:1 [ 0 => "angelderma95@gmail.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" => "J.M." "apellidos" => "Calzada González" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 2 => array:3 [ "nombre" => "P." "apellidos" => "Arcos González" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] 3 => array:3 [ "nombre" => "E." "apellidos" => "Rodríguez Díaz" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] ] "afiliaciones" => array:3 [ 0 => array:3 [ "entidad" => "Servicio de Dermatología, Hospital Universitario de Cabueñes, Gijón, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Anatomía Patológica, Hospital Universitario de Cabueñes, Gijón, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Unidad de Investigación en Emergencia y Desastre, Departamento de Medicina, Universidad de Oviedo, Oviedo, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Sífilis secundaria granulomatosa: presentación de un caso sospechado a partir de los hallazgos histológicos" ] ] "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" => 750 "Ancho" => 1005 "Tamanyo" => 148859 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Immunohistochemical staining. Treponemal antibodies, original magnification ×400.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The Spanish National Epidemiology Center/Instituto de Salud Carlos III records the incidence of syphilis and other sexually transmitted infections (STIs) diagnosed in Spain each year. In 2018 (the most recent year for which data were available at the time of writing), a total of 5079 syphilis cases were diagnosed in Spain. This figure is 6.7 times the mean incidence reported between 1996 and 2001.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> Considering the growing number of syphilis cases and the importance of early diagnosis, it is essential to contemplate syphilis in multiple differential diagnoses.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> We present a case of granulomatous secondary syphilis, a rare variant that is clinically and histologically challenging to diagnose. We also illustrate the usefulness of immunohistochemistry in this setting.</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 51-year-old, heterosexual, cisgender woman of Spanish nationality, with no known allergies or other history of interest, was seen at our department for a 15-day history of a mildly pruritic rash that had begun on the abdomen and spread to the proximal limbs. She had not experienced fever or any other systemic symptoms. She did not mention any lesions on the genitalia or oral mucosa and had not taken any drugs before the onset of the rash. She reported being in a closed relationship with a stable partner, a cisgender male at no obvious risk for STIs.</p><p id="par0015" class="elsevierStylePara elsevierViewall">Physical examination revealed a papular, nonscaling rash consisting of dozens of pink spots with a diameter of between 3 and 10<span class="elsevierStyleHsp" style=""></span>mm that were located predominantly on the abdomen (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>) but also extended to the top of the limbs. The palms and soles were spared. The external genitalia and oral mucosa were also unaffected, and there were no palpable lymph nodes. The entities considered in the clinical differential diagnosis were atypical pityriasis lichenoides, lymphomatoid papulosis, and pityriasis rosea.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">In the histopathologic study, hematoxylin-eosin staining showed a normal epidermis and a predominantly perivascular nodular inflammatory infiltrate in the upper dermis comprising histiocytic cells, several multinucleated giant cells, epithelioid cells, lymphocytes, and abundant plasma cells; there was no evidence of caseous degeneration (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>A). Clusters of mononuclear cells with abundant plasma cells surrounding small vessels were seen in the mid dermis, with endothelial edema and swelling (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>B and C). Specific immunohistochemical staining for <span class="elsevierStyleItalic">Treponema pallidum</span> revealed abundant intracellular and extracellular helical structures (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>).</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">The enzyme-linked immunosorbent assay and <span class="elsevierStyleItalic">Treponema pallidum</span> hemagglutination test were positive, as was the rapid plasma reagin (RPR) test, with a titer of 1:32. HIV serology was negative. Given the presence of granulomas on histology (these are much more common in late phases of syphilis than in secondary syphilis), 3 doses of benzathine penicillin 2.4 million international units were administered over 3 consecutive weeks (1 dose a week). The skin lesions disappeared several days after the last dose and the subsequent serologic response was adequate (RPR titer of 1:2 at 6 months). The patient's partner (the only other contact reported) was tested and was also positive. He received similar treatment at another center. Since both patients denied any other contacts, wider contact tracing was not possible.</p><p id="par0030" class="elsevierStylePara elsevierViewall">The latest analysis of trends in STIs published by the Spanish National Epidemiology Center shows a significant growth in syphilis cases since 2016.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> We are thus increasingly likely to be faced with any of the multiple manifestations of syphilis in routine care. We have described a case of granulomatous secondary syphilis presenting predominantly as nonscaling papules with sparing of the palms and soles. Granulomatous inflammation in syphilis has been linked to advanced stages of the disease and is very uncommon in secondary syphilis.<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3–6</span></a> A high index of clinical suspicion and early diagnosis are key to clinical and epidemiological control, as early phases of the disease (primary and secondary syphilis) are infectious.<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> As occurred in our case, full contact tracing is often not possible.<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> Considering that syphilis has clinical and histologic similarities to a broad range of diseases and conditions, it should be contemplated in multiple differential diagnoses.<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The incidence of syphilis continues to grow in Spain. High clinical suspicion and treatment of early phases are essential for achieving clinical and epidemiological control. Considering its multiple clinical and histopathologic variants, syphilis should not be forgotten in the list of differential diagnoses in the dermatology clinic. Immunohistochemical techniques can be very useful in atypical cases.<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0005" "titulo" => "Conflicts of Interest" ] 1 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "multimedia" => array:3 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 678 "Ancho" => 905 "Tamanyo" => 56792 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Papular rash on the abdomen.</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" => 1186 "Ancho" => 1674 "Tamanyo" => 583465 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Hematoxylin-eosin staining. Original magnification ×40 (A), ×200 (B), and ×400 (C).</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" => 750 "Ancho" => 1005 "Tamanyo" => 148859 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Immunohistochemical staining. Treponemal antibodies, original magnification ×400.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:10 [ 0 => array:3 [ "identificador" => "bib0055" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:1 [ "titulo" => "Unidad de vigilancia del VIH, hepatitis y conductas de riesgo. Vigilancia epidemiológica de las infecciones de transmisión sexual, 2018. 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año/Mes | Html | Total | |
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2024 Noviembre | 20 | 20 | 40 |
2024 Octubre | 107 | 62 | 169 |
2024 Septiembre | 134 | 55 | 189 |
2024 Agosto | 151 | 78 | 229 |
2024 Julio | 93 | 64 | 157 |
2024 Junio | 101 | 38 | 139 |
2024 Mayo | 87 | 72 | 159 |
2024 Abril | 73 | 34 | 107 |
2024 Marzo | 54 | 38 | 92 |
2024 Febrero | 67 | 39 | 106 |
2024 Enero | 59 | 33 | 92 |
2023 Diciembre | 52 | 17 | 69 |
2023 Noviembre | 79 | 105 | 184 |
2023 Octubre | 48 | 36 | 84 |
2023 Septiembre | 58 | 26 | 84 |
2023 Agosto | 70 | 20 | 90 |
2023 Julio | 87 | 28 | 115 |
2023 Junio | 70 | 31 | 101 |
2023 Mayo | 60 | 25 | 85 |
2023 Abril | 45 | 26 | 71 |
2023 Marzo | 68 | 29 | 97 |
2023 Febrero | 32 | 24 | 56 |
2023 Enero | 47 | 37 | 84 |
2022 Diciembre | 236 | 48 | 284 |
2022 Noviembre | 140 | 47 | 187 |
2022 Octubre | 53 | 64 | 117 |