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Perianal Langerhans-Cell Histiocytosis: Review of the Literature

Langerhans-cell histiocytosis (LCH) is a rare disorder characterized by the proliferation of Langerhans cells, which originate in the bone marrow. It presents in two main clinical forms: single system LCH (SS-LCH), when the disease involves a single organ or system, and multisystem LCH (MS-LCH), whi...

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Autors principals: Carlos Augusto Real Martinez, Fabio Guilherme Campos, Fernando Forghieri Silveira, Camila Nardi, Luana Borges Segantine Martins, Naualy Cunha Alencar, Evaldo Pasquini Landi, José Aires Pereira, Danilo Toshio Kanno
Format: Artigo
Idioma:Inglês
Publicat: Thieme Revinter Publicações Ltda. 2026-01-01
Col·lecció:Journal of Coloproctology
Matèries:
histiocytosis
Langerhans-cell
Letterer-Siwe disease
Anus neoplasms
fatal outcome
Accés en línia:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0046-1820490
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