Ravulizumab monotherapy for anti-CFH antibody-associated aHUS in an elderly patient: a case report highlighting individualized clinical decision-making.

CEN Case RepOct 27, 2026 (epub)
Case ReportNephrologyHematologyOpen access

Ryuichi Yoshii, Kengo Kajiwara, Keitaro Hirose et al.

✦ AI-curated · Sources linked

Case in brief

An 85-year-old man presented with acute kidney injury, thrombocytopenia, microangiopathic hemolytic anemia, and severe hypertension. Preserved ADAMTS13 activity and no identified secondary cause supported suspected complement-mediated thrombotic microangiopathy, but anti-CFH antibody results were unavailable during initial treatment decisions. Ravulizumab monotherapy was chosen after individualized assessment of the risks of plasma exchange and immunosuppression. Hematological parameters improved and renal function recovered sufficiently to stop hemodialysis. Subsequent testing found elevated anti-CFH antibodies and no pathogenic complement gene variants, confirming anti-CFH antibody-associated aHUS.

What made this case unusual

The diagnosis was confirmed only after treatment began, and the patient’s age and uncertainty about renal recovery complicated decisions about plasma exchange and immunosuppression. Ravulizumab was selected as an initial monotherapy approach in this context.

Diagnostic / clinical pearl

In suspected complement-mediated TMA, anti-CFH antibody results may not be available when treatment decisions are needed; interpret renal and hematological trends in context, particularly during hemodialysis.

Why it matters

The report emphasizes documenting patient-specific risks when selecting an initial approach and following anti-CFH antibody levels, with immunosuppression considered if titers persist or relapse risk remains high.

Source

Published in CEN Case Rep. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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