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Adult Langerhans Cell Histiocytosis with Hepatic and Pulmonary Involvement
Langerhans cell histiocytosis (LCH) is a rare proliferative disorder of Langerhans cells of unknown etiology. It can involve multiple organ systems with different clinical presentation, which complicates the diagnosis. It can range from isolated to multisystem disease with different prognosis. Altho...
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| Vydáno v: | Case Rep Radiol |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hindawi Publishing Corporation
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4419232/ https://ncbi.nlm.nih.gov/pubmed/25977828 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/536328 |
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