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Acta Med Port ; 24 Suppl 3: 713-4, 2011 Dec.
Artigo em Português | MEDLINE | ID: mdl-22856419

RESUMO

Langerhans cell histiocytosis (LCH) is a rare systemic disorder, with a diversified presentation and natural history. It can compromise any organ. We report a case of a 32-year-old woman who came to our clinic with an asymptomatic palpable breast mass. She underwent excisional biopsy. Immunohistochemical and pathological evaluation revealed Langerhans cell histiocytosis. No multisystem involvement was found.


Assuntos
Doenças Mamárias/patologia , Histiocitose de Células de Langerhans/patologia , Adulto , Feminino , Humanos
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