Systemic sclerosis presenting TAFRO syndrome-like manifestations including renal glomerular microangiopathy: a case report and literature review
Hiroyuki Kawahara; Satoshi Hara; Noriko Iwaki; Hiroko Ikeda; Dai Inoue; Ichiro Mizushima; Hideki Nomura; Yasufumi Masaki · 2025 · Immunological Medicine
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
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Abstract
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 diagnosis of TAFRO syndrome. However, her clinical course and pathological findings, including renal glomerular microangiopathy, were consistent with TAFRO syndrome. We performed a systematic review of the literature to evaluate how autoimmunity affects the clinical characteristics of TAFRO syndrome/i
Abstract by Hiroyuki Kawahara; Satoshi Hara; Noriko Iwaki; Hiroko Ikeda; Dai Inoue; Ichiro Mizushima; Hideki Nomura; Yasufumi Masaki, Immunological Medicine (2025) — licensed CC BY 4.0.
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Metadata source: DOAJ · DOI 10.1080/25785826.2025.2481675