Acral pseudolymphomatous angiokeratoma: case report and literature review
The authors describe a case of a female patient with Acral Pseudolymphomatous Angiokeratoma of Children, known as APACHE. It is a rare benign cutaneous disease, of unknown etiology, characterized by multiple, asymptomatic erythematous-violaceous papules and nodules, usually located unilaterally with acral distribution. Today, this denomination is questionable, since there are published reports of this disease in adults and in different locations. Clinically, it is similar to an angiokeratoma, whereas hystologically, it corresponds to a distinct type of pseudolymphoma. The immunohistochemical study is required to distinguish APACHE from cutaneous lymphoma.
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Sociedade Brasileira de Dermatologia
2013
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oai:scielo:S0365-059620130008000392014-06-16Acral pseudolymphomatous angiokeratoma: case report and literature reviewLessa,Priscila PachecoJorge,Juliana Chaib FerreiraFerreira,Flávia ReginaLira,Marcia Lanzoni de AlvarengaMandelbaum,Samuel Henrique Child Extremities Hemangioma Pseudolymphoma The authors describe a case of a female patient with Acral Pseudolymphomatous Angiokeratoma of Children, known as APACHE. It is a rare benign cutaneous disease, of unknown etiology, characterized by multiple, asymptomatic erythematous-violaceous papules and nodules, usually located unilaterally with acral distribution. Today, this denomination is questionable, since there are published reports of this disease in adults and in different locations. Clinically, it is similar to an angiokeratoma, whereas hystologically, it corresponds to a distinct type of pseudolymphoma. The immunohistochemical study is required to distinguish APACHE from cutaneous lymphoma.info:eu-repo/semantics/openAccessSociedade Brasileira de DermatologiaAnais Brasileiros de Dermatologia v.88 n.6 suppl.1 20132013-12-01info:eu-repo/semantics/reporttext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000800039en10.1590/abd1806-4841.20132413 |
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Lessa,Priscila Pacheco Jorge,Juliana Chaib Ferreira Ferreira,Flávia Regina Lira,Marcia Lanzoni de Alvarenga Mandelbaum,Samuel Henrique |
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Lessa,Priscila Pacheco Jorge,Juliana Chaib Ferreira Ferreira,Flávia Regina Lira,Marcia Lanzoni de Alvarenga Mandelbaum,Samuel Henrique Acral pseudolymphomatous angiokeratoma: case report and literature review |
author_facet |
Lessa,Priscila Pacheco Jorge,Juliana Chaib Ferreira Ferreira,Flávia Regina Lira,Marcia Lanzoni de Alvarenga Mandelbaum,Samuel Henrique |
author_sort |
Lessa,Priscila Pacheco |
title |
Acral pseudolymphomatous angiokeratoma: case report and literature review |
title_short |
Acral pseudolymphomatous angiokeratoma: case report and literature review |
title_full |
Acral pseudolymphomatous angiokeratoma: case report and literature review |
title_fullStr |
Acral pseudolymphomatous angiokeratoma: case report and literature review |
title_full_unstemmed |
Acral pseudolymphomatous angiokeratoma: case report and literature review |
title_sort |
acral pseudolymphomatous angiokeratoma: case report and literature review |
description |
The authors describe a case of a female patient with Acral Pseudolymphomatous Angiokeratoma of Children, known as APACHE. It is a rare benign cutaneous disease, of unknown etiology, characterized by multiple, asymptomatic erythematous-violaceous papules and nodules, usually located unilaterally with acral distribution. Today, this denomination is questionable, since there are published reports of this disease in adults and in different locations. Clinically, it is similar to an angiokeratoma, whereas hystologically, it corresponds to a distinct type of pseudolymphoma. The immunohistochemical study is required to distinguish APACHE from cutaneous lymphoma. |
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Sociedade Brasileira de Dermatologia |
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2013 |
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http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000800039 |
work_keys_str_mv |
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1756412454917636096 |