Langerhans Cell Histiocytosis of the Gastrointestinal Tract – A Rare Entity

Langerhans cell histiocytosis (LCH) is an idiopathic and rare disease that ranges in clinical severity based on location and organ involvement. LCH most commonly affects the skin and bones. The involvement of the gastrointestinal tract (GI) in adults is exceedingly rare and only 10 cases have been r...

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Detalles Bibliográficos
Autores principales: Bhinder, Jasmine, Mori, Amit, Kurtz, Leon, Reddy, Madhavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2018
Materias:
Gastroenterology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919765/
https://www.ncbi.nlm.nih.gov/pubmed/29713572
http://dx.doi.org/10.7759/cureus.2227

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919765/
https://www.ncbi.nlm.nih.gov/pubmed/29713572
http://dx.doi.org/10.7759/cureus.2227

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