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Erdheim-Chester disease with isolated craniocerebral involvement
Erdheim-Chester disease (ECD) is a rare non-Langerhans form of histiocytosis with distinctive radiographic and pathological features. Intracranial involvement is further a rarity, usually producing diabetes insipidus or cerebellar-brainstem symptoms. We report a 40-year-old man presenting with recur...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Publishing Group
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3645836/ https://ncbi.nlm.nih.gov/pubmed/23592809 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2012-006823 |
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