Acquired Thrombotic Thrombocytopenic Thrombocytopenia Presenting As Urinary Tract Infection and Perianal Abscess: A Case Review
Oluwaremilekun Tolu-Akinnawo, Kikelola Oyeleye, Ikenna Nnamani

TL;DR
A rare case of acquired TTP triggered by a urinary tract infection and perianal abscess is described, highlighting the importance of early diagnosis and treatment.
Contribution
This case report presents a rare clinical scenario of infection-induced TTP and emphasizes early suspicion for better outcomes.
Findings
The patient presented with UTI and perianal abscess, which triggered acquired TTP.
ADAMTS13 levels were <5% with an inhibitor, confirming the TTP diagnosis.
Treatment with steroids, plasma exchange, and Rituximab led to a swift recovery.
Abstract
Thrombotic thrombocytopenic purpura (TTP) is a rare but potentially life-threatening hematologic disorder characterized by hemolytic anemia, thrombocytopenia, renal failure, fever, and neurologic dysfunction. While cases often do not present with all five characteristics (<5%), TTP can be hereditary or acquired, often due to a deficiency or dysfunction of the ADAMST13 enzyme. Here, we describe a case of infection-induced acquired TTP in a middle-aged male with urinary tract infection (UTI) and perianal abscess. Suspicion arose from hematologic abnormalities, fever, thrombocytopenia, acute renal failure, and the presence of an underlying infection. A PLASMIC score of 6 (indicating a 72% probability of ADAMTS13 deficiency) prompted ADAMTS13 level testing, revealing levels <5% with the presence of an inhibitor, confirming TTP diagnosis. Treatment with high-dose steroids and daily plasma…
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Taxonomy
TopicsComplement system in diseases · Burkholderia infections and melioidosis · Renal Diseases and Glomerulopathies
