Erdheim-Chester Disease: Case Report
Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis characterized by the infiltration of bone and multiple organs by foamy lipid-laden histiocytes. ECD is easy to be misdiagnosed due to its complicated clinical manifestations. We report a patient who visited the hospital due to...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Chinês |
| Vydáno: |
Editorial Office of Journal of Rare Diseases
2022-01-01
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| Edice: | 罕见病研究 |
| Témata: | |
| On-line přístup: | https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2022.01.011 |
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