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Systemic sclerosis presenting TAFRO syndrome-like manifestations including renal glomerular microangiopathy: a case report and literature review

TAFRO syndrome is a systemic inflammatory disorder of unknown etiology, and its diagnosis requires the exclusion of autoimmune diseases. A 42-year-old Japanese woman presented with TAFRO syndrome-like manifestations, but had undiagnosed limited-cutaneous systemic sclerosis preventing a definitive di...

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Hlavní autoři: Hiroyuki Kawahara, Satoshi Hara, Noriko Iwaki, Hiroko Ikeda, Dai Inoue, Ichiro Mizushima, Hideki Nomura, Yasufumi Masaki, Yasunori Iwata, Mitsuhiro Kawano
Médium: Artigo
Jazyk:Inglês
Vydáno: Taylor & Francis Group 2025-10-01
Edice:Immunological Medicine
Témata:
TAFRO syndrome
iMCD-TAFRO
systemic sclerosis
autoantibody
autoimmunity
On-line přístup:https://www.tandfonline.com/doi/10.1080/25785826.2025.2481675
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