ArticleCureus2026
Therapeutic Plasma Exchange in a 15-kg Child With Atypical Hemolytic Uremic Syndrome: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
6 authors.
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Abstract
Atypical hemolytic uremic syndrome (aHUS) is one of the thrombotic microangiopathy (TMA) syndromes characterized by thrombocytopenia, Coombs-negative hemolytic anemia, and renal dysfunction without evidence of Shiga toxin-producing Escherichia coli (E. coli) (STEC) or thrombotic thrombocytopenic purpura (TTP). aHUS is a rare, potentially fatal entity. We present a case of a six-year-old male with vomiting and abdominal pain who developed hematuria and jaundice, along with acute kidney injury (AKI). The patient was diagnosed with aHUS and managed with plasma infusions and exchange, immunosuppression, hemodialysis, and associated kidney-protective measures. He successfully achieved remission and was discharged after a prolonged hospital stay.
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