Adult Langerhans Cell Histiocytosis with Hepatic and Pulmonary Involvement

Langerhans cell histiocytosis (LCH) is a rare proliferative disorder of Langerhans cells of unknown etiology. It can involve multiple organ systems with different clinical presentation, which complicates the diagnosis. It can range from isolated to multisystem disease with different prognosis. Altho...

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Detalles Bibliográficos
Autores principales: Araujo, Bruno, Costa, Francisco, Lopes, Joanne, Castro, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419232/
https://www.ncbi.nlm.nih.gov/pubmed/25977828
http://dx.doi.org/10.1155/2015/536328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419232/
https://www.ncbi.nlm.nih.gov/pubmed/25977828
http://dx.doi.org/10.1155/2015/536328

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