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An autopsy case of TAFRO syndrome with membranoproliferative glomerulonephritis-like lesions
TAFRO syndrome (thrombocytopenia, anasarca, myelofibrosis, renal dysfunction, and organomegaly) is an atypical manifestation of multicentric Castleman’s disease. Although overproduction of interleukin-6, vascular endothelial growth factor, and other cytokines may partially explain the pathophysiolog...
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| Published in: | CEN Case Rep |
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| Main Authors: | , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Springer Singapore
2018
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6361076/ https://ncbi.nlm.nih.gov/pubmed/30244358 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-018-0363-9 |
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