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2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Orcein stain was positive only in the areas with abnormal elastic fibers&#44; including some within the stratum corneum&#46; Orcein stain also revealed altered elastic fibers &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Elastosis perforans serpiginosa&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Two sessions of cryotherapy were administered at an interval of 6 weeks&#46; 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A keratin plug can sometimes be observed on the surface&#44; and there many be multinucleated giant cells and a pericanalicular inflammatory infiltrate&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Specific stains for elastic fibers &#40;Verhoeff-Van Gieson or orcein&#41; show the abnormal morphology of these elastic fibers&#46; In penicillamine-induced cases&#44; slight differences can be seen on optical and electron microscopy&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The etiology and pathogenesis of EPS are unknown&#46; It is thought that the abnormal fibers may be identified as foreign bodies&#44; provoking a granulomatous reaction that results in their elimination&#46; The granulomatous reaction around the elastic fibers may play an important role in the pathophysiology of elastosis perforans serpiginosa&#44; as may the keratinocytes that surround the elastotic material and express the elastin receptor &#40;67-kDa&#41;&#46; This receptor could be implicated in the interaction of the keratinocytes with the elastin and its subsequent elimination&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis principally includes granuloma annulare&#44; prurigo nodularis&#44; tinea&#44; annular sarcoidosis&#44; cutaneous calcinosis&#44; and porokeratosis of Mibelli&#46; Histopathologically&#44; EPS must be distinguished from congenital reactive perforating collagenosis&#8212;a rare genodermatosis usually of autosomal dominant inheritance that typically occurs in association with renal dysfunction or diabetes mellitus&#8212;and the acquired forms &#40;Kyrle disease and perforating folliculitis&#41;&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Most forms of treatment are unsatisfactory although good cosmetic results have been achieved with cryotherapy&#44;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> electrocoagulation&#44; 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Case for Diagnosis
Asymptomatic Lesion on the Forehead
Lesión asintomática en la región frontal
V. Fuentelsaz-del Barrioa,
Autor para correspondencia
victoriafuentelsaz@hotmail.com

Corresponding author.
, A. Pulidoa, V. Parrab
a Servicio de Dermatología, Hospital Gregorio Marañón, Madrid, Spain
b Servicio de Anatomía Patológica, Hospital Gregorio Marañón, Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 54-year-old man with a history of hypertension on treatment with enalapril and simvastatin consulted for the appearance of an asymptomatic lesion that had appeared on the right frontal region 4 months earlier and that had increased progressively in size&#46; He reported no local trauma or use of topical treatments&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">An irregular plaque of normal skin color&#44; measuring 1 x 0&#46;8<span class="elsevierStyleHsp" style=""></span>cm and with a slightly depressed centre was observed&#59; it was formed of small papules following a serpiginous path in the periphery of the lesion&#46; No other lesions of interest were observed on other areas of the body &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">A biopsy taken from the border of the lesion revealed an accumulation of acellular eosinophilic material associated with thick hypereosinophilic elastic fibers in the superficial papillary dermis&#46; There was a moderate inflammatory infiltrate of lymphocytes and plasma cells in the adjacent dermis&#44; with frequent multinucleated giant cells&#46; One area of the overlying epidermis presented a perforation and there was transepidermal elimination of the acellular eosinophilic material associated with small clusters of neutrophils &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Orcein stain was positive only in the areas with abnormal elastic fibers&#44; including some within the stratum corneum&#46; Orcein stain also revealed altered elastic fibers &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Elastosis perforans serpiginosa&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Two sessions of cryotherapy were administered at an interval of 6 weeks&#46; Three months after the second session&#44; the skin on the treated area was slightly atrophied and hypopigmented&#46; At 9 months of follow-up there was no recurrence and no new lesions had appeared&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Elastosis perforans serpiginosa is a rare dermatosis caused by the transepidermal elimination of thickened elastic fibers&#46; It has traditionally been classified into 3 types&#58; idiopathic&#59; secondary to treatment with D-penicillamine&#59; and associated with other disorders such as Down syndrome&#44; Marfan syndrome&#44; osteogenesis imperfecta&#44; Ehlers-Danlos syndrome&#44; acrogeria&#44; morphea&#44; Rothmund-Thomson syndrome&#44; and pseudoxanthoma elasticum&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a> Some familial cases have also been described&#44; with variable inheritance patterns&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The lesions typically appear in early adulthood&#44; with a male to female ratio of 4 to 1&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Clinically&#44; elastosis perforans serpiginosa consists of the appearance of asymptomatic or slightly pruritic&#44; skin colored or erythematous papules with a central keratin plug&#59; bleeding occurs if the plug is removed&#46; The papules tend to occur in a curvilinear or serpiginous distribution&#44; preferentially on the face&#44; neck&#44; or extremities&#46; The lesions sometimes resolve spontaneously after months or even years&#44; leaving hypopigmented atrophic scars&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Histological features include the presence of abnormal&#44; thickened elastic fibers that are eliminated via transepidermal channels that form grooves in an acanthotic epidermis&#46; A keratin plug can sometimes be observed on the surface&#44; and there many be multinucleated giant cells and a pericanalicular inflammatory infiltrate&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Specific stains for elastic fibers &#40;Verhoeff-Van Gieson or orcein&#41; show the abnormal morphology of these elastic fibers&#46; In penicillamine-induced cases&#44; slight differences can be seen on optical and electron microscopy&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The etiology and pathogenesis of EPS are unknown&#46; It is thought that the abnormal fibers may be identified as foreign bodies&#44; provoking a granulomatous reaction that results in their elimination&#46; The granulomatous reaction around the elastic fibers may play an important role in the pathophysiology of elastosis perforans serpiginosa&#44; as may the keratinocytes that surround the elastotic material and express the elastin receptor &#40;67-kDa&#41;&#46; This receptor could be implicated in the interaction of the keratinocytes with the elastin and its subsequent elimination&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis principally includes granuloma annulare&#44; prurigo nodularis&#44; tinea&#44; annular sarcoidosis&#44; cutaneous calcinosis&#44; and porokeratosis of Mibelli&#46; Histopathologically&#44; EPS must be distinguished from congenital reactive perforating collagenosis&#8212;a rare genodermatosis usually of autosomal dominant inheritance that typically occurs in association with renal dysfunction or diabetes mellitus&#8212;and the acquired forms &#40;Kyrle disease and perforating folliculitis&#41;&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Most forms of treatment are unsatisfactory although good cosmetic results have been achieved with cryotherapy&#44;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> electrocoagulation&#44; tazarotene&#44; imiquimod&#44; subcutaneous hydrocortisone&#44; cellophane tape stripping&#44; bichloroacetic acid&#44; carbon-dioxide laser&#44; and oral isotretinoin&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">The interesting feature in this case of elastosis perforans serpiginosa is the unusually late onset and presentation in the form of a single lesion&#46; We believe that further lesions may appear in the future despite the good initial response to cryotherapy&#46;</p></span></span>"
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Información del artículo
ISSN: 15782190
Idioma original: Inglés
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