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Hepatic Langerhans Cell Histiocytosis (LCH) Presenting as a Harbinger of Multisystem LCH

Langerhans cell histiocytosis (LCH) is a rare systemic disorder characterized by an infiltration of CD1a+/langerin+ histiocytes, commonly involving bone, skin, and lymph nodes in children. Hepatic involvement is rarely observed in multisystem LCH. We describe an exceptional case of hepatic LCH in an...

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Detalles Bibliográficos
Autores principales:	Li, Hua, Ells, Peter, Arslan, Mustafa Erdem, Robstad, Karl A, Lee, Hwajeong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2020
Materias:	Pathology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359969/ https://www.ncbi.nlm.nih.gov/pubmed/32676232 http://dx.doi.org/10.7759/cureus.8591

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