Multisystemic Langerhans cell histiocytosis: case report

ABSTRACT Langerhans cell histiocytosis is the designated name for a spectrum of rare diseases that affects children from one- to three-years-old, which name refers to the proliferation of cells morphologically and immunophenotypically similar to the specialized dendritic cells of the skin and mucosa...

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Main Authors: Larissa A. Paiva (Author), Daniela M. Takano (Author), Valeska A. S. Queiroz (Author), Laís S. Príncipe (Author)
Format: Book
Published: Sociedade Brasileira de Patologia Clínica.
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Summary:ABSTRACT Langerhans cell histiocytosis is the designated name for a spectrum of rare diseases that affects children from one- to three-years-old, which name refers to the proliferation of cells morphologically and immunophenotypically similar to the specialized dendritic cells of the skin and mucosa (Langerhans cells). This article reports a case of multisystemic Langerhans cell histiocytosis diagnosed by autopsy of a four-day newborn with confirmation by immunohistochemistry and secondary systemic infection associated.
Item Description:1676-2444
1678-4774
10.5935/1676-2444.20160066