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Langerhans cell histiocytosis masquerading as acute appendicitis: Case report and review
Langerhans cell histiocytosis (LCH) is a rare syndrome characterized by unifocal, multifocal unisystem, or disseminated/multi-system disease that commonly involves the bone, skin, lymph nodes, pituitary, or sometimes lung (almost exclusively in smokers) causing a variety of symptoms from rashes and...
Gardado en:
| Publicado en: | World J Gastrointest Endosc |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Baishideng Publishing Group Inc
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5355761/ https://ncbi.nlm.nih.gov/pubmed/28360976 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4253/wjge.v9.i3.139 |
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