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Erdheim–Chester Disease With Multiorgan Involvement, Following Polycythemia Vera: A Case Report
Erdheim–Chester disease is a rare form of non-Langerhans cell histiocytosis characterized by the migration and infiltration of lipid-laden CD68(+), CD1a(−) and S100(−) histiocytes to various target organs, which leads to the disruption of physiological tissue architecture and reactive fibrosis, and...
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| Yayımlandı: | Medicine (Baltimore) |
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| Asıl Yazarlar: | , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Wolters Kluwer Health
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4902423/ https://ncbi.nlm.nih.gov/pubmed/27196481 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000003697 |
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