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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2018
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| 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 |