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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...
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| 出版年: | Cureus |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Cureus
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5919765/ https://ncbi.nlm.nih.gov/pubmed/29713572 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.2227 |
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