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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Bibliographic Details
Published in:CEN Case Rep
Main Authors: Hashimoto, Keiko, Sano, Takashi, Honma, Yukari, Ida, Maoko, Tominaga, Hiroshi, Sawada, Aya, Abe, Tetsuya, Takahashi, Haruka, Shimada, Yoshitaka, Masaki, Takanori, Kamata, Mariko, Naito, Shokichi, Aoyama, Togo, Takeuchi, Yasuo, Akiya, Masashi, Inukai, Madoka, Nakata, Norihiro
Format: Artigo
Language:Inglês
Published: Springer Singapore 2018
Subjects:
Case Report
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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