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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We report the case of a 38-year-old woman &#40;skin type V&#41; with a history of tricuspid and mitral regurgitation who had undergone pulmonary bilobectomy for atypical carcinoid tumor&#46; She was taking oral contraceptives&#46; She attended our center with a flare-up of pruriginous lesions on her hands and forearms that had first appeared 1 year previously&#46; The lesions appeared every month and did not remit completely between flare-ups&#44; although they did improve with medium-potency topical corticosteroids&#46; She reported no lesions at other sites and denied having had concomitant symptoms&#46; Physical examination revealed poorly defined&#44; apparently residual erythematous-brownish macules on the anterior and lateral surfaces of the wrists&#46; Multiple hyperpigmented papules with a shiny surface measuring between 1&#160;mm and 3<span class="elsevierStyleHsp" style=""></span>mm in diameter were observed on the radial surface of the first finger of both hands and on the palmar creases&#46; These alternated with flesh-colored papules with a lichenoid appearance on the adjacent skin and were distributed symmetrically &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; An ultrasound scan &#40;Esaote&#44; MyLabClass C with a 22-MHz transducer&#41; of the affected area on the lateral surface of the wrist revealed epidermal thickening in the form of a cleft&#44; which was observed as double hyperechoic band with a hypoechoic central area&#46; The upper band was characterized by undulations that varied between more hyperechoic areas &#40;convex&#41; and more hypoechoic areas &#40;concave&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Ultrasound revealed a certain degree of hypoechogenicity in the dermis that was interpreted as an artifact resulting from epidermal thickening using the 22-MHz transducer&#46; The suspicion of lichen nitidus compared with elastic fiber abnormality led us to perform a biopsy of the ultrasound lesion and to prescribe clobetasol cream&#46; Histopathology revealed a compact area of orthokeratotic hyperkeratosis resting on a slight epidermal depression with mild hypergranulosis in the epidermis &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; No inflammation or other significant histopathological abnormalities were observed&#46; Orcein staining did not reveal elastorrhexis&#46; Therefore&#44; the findings were compatible with focal acral hyperkeratosis &#40;FAH&#41;&#8211;type marginal papular acrokeratoderma&#46; At subsequent visits&#44; the patient reported a lack of improvement with her daily high-potency corticosteroid and even mentioned the appearance of additional lesions&#59; consequently&#44; we recommended a switch to mometasone and calcipotriol cream&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">FAH is an uncommon variant of a heterogeneous group of conditions grouped together under the term <span class="elsevierStyleItalic">palmoplantar keratoderma</span>&#44; which are characterized by chronic pathologic thickening of the hairless skin of the palms and soles secondary to hyperkeratosis&#46; Until 1983&#44; there had been multiple reports of hyperkeratotic papular lesions on the lateral sides of the hands and feet&#46; Their clinical presentation was similar to that of a condition previously known as acrokeratoelastoidosis&#44;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> and the histology findings were similar&#44; except for the absence of elastorrhexis&#46; This is when Dowd et al&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> coined the term <span class="elsevierStyleItalic">focal acral hyperkeratosis</span> to define a new entity whose differentiation with acrokeratoelastoidosis continues to be controversial&#46; Those authors who see the conditions as separate entities believe that the first is a focal keratinization disorder&#44; whereas the second is based on abnormalities of the elastic fibers&#46; Their claims are supported by the histologic nuance of elastorrhexis&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> In 1994&#44; Rongioletti et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> proposed grouping these 2<span class="elsevierStyleHsp" style=""></span>entities and other clinically indistinguishable conditions under the term <span class="elsevierStyleItalic">marginal papular acrokeratoderma</span>&#46; In 2009&#44; Mart&#237;nez-Casimiro et al&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">5</span></a> reported a new FAH-type case&#44; similar to the one we report here&#46; The patient was a black woman in the third decade of life with asymptomatic lesions on the palms and lateral surfaces of the hands that had first appeared several years previously&#46; The authors studied the article by Dowd et al&#46;&#44; who reported on familial cases &#40;autosomal dominant inheritance pattern<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">6</span></a>&#41;&#46; The typical histology pattern is invariably characterized by orthokeratotic hyperkeratosis on an epidermal depression&#44; with no abnormalities of collagen or elastic fibers&#46; Lee and Kim<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">7</span></a> examined biopsy specimens of lesional and healthy skin and performed immunohistochemical staining of proliferation and differentiation markers &#40;Ki-67&#47;proliferating cell nuclear antigen and involucrin&#44; respectively&#41;&#46; In addition to a 3&#46;4-fold increase in the thickness of the orthokeratotic layer and a 2-fold increase in the thickness of the epidermis&#44; the authors reported increased levels for both markers&#44; thus supporting the possibility that FAH is a focal disorder of keratinization in which the process is accelerated&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">In addition to the histology findings&#44; we reported the ultrasound characteristics of the condition&#44; which involved a specific epidermal cleft with marked changes in echogenicity and no abnormalities in the dermis&#46; No abnormalities of the healthy skin were observed &#40;the marked difference in the thickness of the epidermis can be seen in <a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; To date&#44; diagnosis of FAH has been based on characteristic symptoms with consistent demographic data and a potentially compatible family history&#44; as well as on the absence of dermal abnormalities in histology&#46; The finding of the ultrasound characteristics used in the differential diagnosis<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">8</span></a> of FAH &#40;acrokeratoelastoidosis itself&#44; plane warts&#44; acrokeratosis verruciformis&#44; punctate porokeratosis&#44; punctate palmoplantar keratoderma&#44; palmoplantar lichen planus&#44; and juvenile elastoma&#41; could be essential for determining the role of ultrasound in the differential diagnosis of these conditions&#46; The main limitation is the low number of cases and&#44; therefore&#44; the difficulty in matching with similar clinical presentations in the various conditions that manifest as palmoplantar keratoderma&#46; There is no evidence to support treating FAH&#44; which often proves to be ineffective&#58; given the absence of symptoms&#44; not treating is a reasonable option&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">9</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">We report the first ultrasound description of FAH as an additional diagnostic tool in the study of palmoplantar keratoderma&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0025" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case and Research Letters
Correlation Between Clinical, Histopathologic, and Ultrasound Findings in Focal Acral Hyperkeratosis
Hiperqueratosis acral focal: correlación clínica, histopatológica y ecográfica
J. Company-Quirogaa,
Autor para correspondencia
j.companyquiroga@gmail.com

Corresponding author.
, B. Echeverríaa, J.C. Tardíob, C. Martínez-Morána
a Servicio de Dermatología, Hospital Universitario de Fuenlabrada, Fuenlabrada (Madrid), España
b Servicio de Anatomía Patológica, Hospital Universitario de Fuenlabrada, Fuenlabrada (Madrid), España
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        "titulo" => "Hiperqueratosis acral focal&#58; correlaci&#243;n cl&#237;nica&#44; histopatol&#243;gica y ecogr&#225;fica"
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">A-C&#44; Minute symmetrically arranged flesh-colored hyperpigmented papules with a shiny surface that is lichenoid in appearance&#44; some of which are umbilicated&#46; D&#41; Hyperpigmentation of the interphalangeal joints with characteristic lesions&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We report the case of a 38-year-old woman &#40;skin type V&#41; with a history of tricuspid and mitral regurgitation who had undergone pulmonary bilobectomy for atypical carcinoid tumor&#46; She was taking oral contraceptives&#46; She attended our center with a flare-up of pruriginous lesions on her hands and forearms that had first appeared 1 year previously&#46; The lesions appeared every month and did not remit completely between flare-ups&#44; although they did improve with medium-potency topical corticosteroids&#46; She reported no lesions at other sites and denied having had concomitant symptoms&#46; Physical examination revealed poorly defined&#44; apparently residual erythematous-brownish macules on the anterior and lateral surfaces of the wrists&#46; Multiple hyperpigmented papules with a shiny surface measuring between 1&#160;mm and 3<span class="elsevierStyleHsp" style=""></span>mm in diameter were observed on the radial surface of the first finger of both hands and on the palmar creases&#46; These alternated with flesh-colored papules with a lichenoid appearance on the adjacent skin and were distributed symmetrically &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; An ultrasound scan &#40;Esaote&#44; MyLabClass C with a 22-MHz transducer&#41; of the affected area on the lateral surface of the wrist revealed epidermal thickening in the form of a cleft&#44; which was observed as double hyperechoic band with a hypoechoic central area&#46; The upper band was characterized by undulations that varied between more hyperechoic areas &#40;convex&#41; and more hypoechoic areas &#40;concave&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Ultrasound revealed a certain degree of hypoechogenicity in the dermis that was interpreted as an artifact resulting from epidermal thickening using the 22-MHz transducer&#46; The suspicion of lichen nitidus compared with elastic fiber abnormality led us to perform a biopsy of the ultrasound lesion and to prescribe clobetasol cream&#46; Histopathology revealed a compact area of orthokeratotic hyperkeratosis resting on a slight epidermal depression with mild hypergranulosis in the epidermis &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; No inflammation or other significant histopathological abnormalities were observed&#46; Orcein staining did not reveal elastorrhexis&#46; Therefore&#44; the findings were compatible with focal acral hyperkeratosis &#40;FAH&#41;&#8211;type marginal papular acrokeratoderma&#46; At subsequent visits&#44; the patient reported a lack of improvement with her daily high-potency corticosteroid and even mentioned the appearance of additional lesions&#59; consequently&#44; we recommended a switch to mometasone and calcipotriol cream&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">FAH is an uncommon variant of a heterogeneous group of conditions grouped together under the term <span class="elsevierStyleItalic">palmoplantar keratoderma</span>&#44; which are characterized by chronic pathologic thickening of the hairless skin of the palms and soles secondary to hyperkeratosis&#46; Until 1983&#44; there had been multiple reports of hyperkeratotic papular lesions on the lateral sides of the hands and feet&#46; Their clinical presentation was similar to that of a condition previously known as acrokeratoelastoidosis&#44;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> and the histology findings were similar&#44; except for the absence of elastorrhexis&#46; This is when Dowd et al&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> coined the term <span class="elsevierStyleItalic">focal acral hyperkeratosis</span> to define a new entity whose differentiation with acrokeratoelastoidosis continues to be controversial&#46; Those authors who see the conditions as separate entities believe that the first is a focal keratinization disorder&#44; whereas the second is based on abnormalities of the elastic fibers&#46; Their claims are supported by the histologic nuance of elastorrhexis&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> In 1994&#44; Rongioletti et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> proposed grouping these 2<span class="elsevierStyleHsp" style=""></span>entities and other clinically indistinguishable conditions under the term <span class="elsevierStyleItalic">marginal papular acrokeratoderma</span>&#46; In 2009&#44; Mart&#237;nez-Casimiro et al&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">5</span></a> reported a new FAH-type case&#44; similar to the one we report here&#46; The patient was a black woman in the third decade of life with asymptomatic lesions on the palms and lateral surfaces of the hands that had first appeared several years previously&#46; The authors studied the article by Dowd et al&#46;&#44; who reported on familial cases &#40;autosomal dominant inheritance pattern<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">6</span></a>&#41;&#46; The typical histology pattern is invariably characterized by orthokeratotic hyperkeratosis on an epidermal depression&#44; with no abnormalities of collagen or elastic fibers&#46; Lee and Kim<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">7</span></a> examined biopsy specimens of lesional and healthy skin and performed immunohistochemical staining of proliferation and differentiation markers &#40;Ki-67&#47;proliferating cell nuclear antigen and involucrin&#44; respectively&#41;&#46; In addition to a 3&#46;4-fold increase in the thickness of the orthokeratotic layer and a 2-fold increase in the thickness of the epidermis&#44; the authors reported increased levels for both markers&#44; thus supporting the possibility that FAH is a focal disorder of keratinization in which the process is accelerated&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">In addition to the histology findings&#44; we reported the ultrasound characteristics of the condition&#44; which involved a specific epidermal cleft with marked changes in echogenicity and no abnormalities in the dermis&#46; No abnormalities of the healthy skin were observed &#40;the marked difference in the thickness of the epidermis can be seen in <a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; To date&#44; diagnosis of FAH has been based on characteristic symptoms with consistent demographic data and a potentially compatible family history&#44; as well as on the absence of dermal abnormalities in histology&#46; The finding of the ultrasound characteristics used in the differential diagnosis<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">8</span></a> of FAH &#40;acrokeratoelastoidosis itself&#44; plane warts&#44; acrokeratosis verruciformis&#44; punctate porokeratosis&#44; punctate palmoplantar keratoderma&#44; palmoplantar lichen planus&#44; and juvenile elastoma&#41; could be essential for determining the role of ultrasound in the differential diagnosis of these conditions&#46; The main limitation is the low number of cases and&#44; therefore&#44; the difficulty in matching with similar clinical presentations in the various conditions that manifest as palmoplantar keratoderma&#46; There is no evidence to support treating FAH&#44; which often proves to be ineffective&#58; given the absence of symptoms&#44; not treating is a reasonable option&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">9</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">We report the first ultrasound description of FAH as an additional diagnostic tool in the study of palmoplantar keratoderma&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0025" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Company-Quiroga J&#44; Echeverr&#237;a B&#44; Tard&#237;o JC&#44; Mart&#237;nez-Mor&#225;n C&#46; Hiperqueratosis acral focal&#58; correlaci&#243;n cl&#237;nica&#44; histopatol&#243;gica y ecogr&#225;fica&#46; Actas Dermosifiliogr&#46; 2018&#59;109&#58;936&#8211;939&#46;</p>"
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          "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Upper trace&#44; epidermis&#59; middle trace&#44; dermis&#59; lower trace&#44; subcutaneous cellular tissue&#46; Lesional skin &#40;left&#41;&#58; cleft in the epidermis seen as a double hyperechoic band with a hypoechoic central area on a somewhat hypoechoic dermis &#40;possible artifact secondary to variability in epidermal thickening&#41;&#46; Upper band&#58; undulation that alternates between more hyperechoic areas &#40;convex&#41; and more hypoechoic areas &#40;concave&#41;&#46; Healthy skin &#40;right&#41;&#58; epidermis with no abnormalities in the form of a fine homogeneous hyperechoic band&#46;</p>"
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          "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">A&#44; Compact orthokeratotic hyperkeratosis resting on a slight epidermal depression with hypergranulosis &#40;hematoxylin-eosin&#44; original magnification&#44; &#215;10&#41;&#46; B&#44; Orcein staining&#44; with no evidence of elastorrhexis or other dermal alterations &#40;orcein&#44; original magnification&#44; &#215;20&#41;&#46;</p>"
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Información del artículo
ISSN: 15782190
Idioma original: Inglés
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