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...

Descripción completa

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

Internet

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

Ejemplares similares