Rare Presentation of Atypical Hemolytic Uremic Syndrome in an Adult
Document Type
Article
Publication Date
9-1-2021
Description
Thrombotic microangiopathies (TMA) are disorders characterized by microangiopathic hemolytic anemia, thrombocytopenia, and microthrombi leading to organ dysfunction. Atypical hemolytic uremic syndrome (aHUS) is a rare subtype of TMA mediated by complement dysregulation. We present a case of a 59-year-old female who presented with acute kidney injury and mild thrombocytopenia but with normal hemoglobin. We highlight the importance of prompt diagnosis of aHUS and initiating appropriate treatment with eculizumab.
Citation Information
Alhabhbeh, Ammar A.; Fatima, Zainab; Thomas, Akesh; and Cook, Christopher, "Rare Presentation of Atypical Hemolytic Uremic Syndrome in an Adult" (2021). ETSU Faculty Works. 126.
https://dc.etsu.edu/etsu-works-2/126