A case of acute pancreatitis-induced microangiopathic hemolytic anemia with thrombocytopenia

Kevin M Hill1,2, Danielle Moorman3,4, Jonathan Mack3,5,4

  • 1Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada. kevhill@toh.ca.

Insights

Microangiopathic hemolytic anemia and thrombocytopenia (MAHA-T) is a rare complication of acute pancreatitis. This case report suggests therapeutic plasma exchange (TPE) may stabilize MAHA-T, even with normal ADAMTS13 levels, warranting further investigation.

Area of Science:

  • Internal Medicine
  • Hematology
  • Gastroenterology

Background:

  • Microangiopathic hemolytic anemia and thrombocytopenia (MAHA-T) is a rare but serious complication of acute pancreatitis (AP).
  • The optimal management and natural history of AP-induced MAHA-T remain poorly understood.
  • Therapeutic plasma exchange (TPE) is frequently employed, but its precise role is unclear.

Observation:

  • A case of acute pancreatitis leading to MAHA-T with end-organ dysfunction and a normal ADAMTS13 level is presented.
  • The patient's condition, blood counts, and hemolytic markers stabilized after three TPE sessions.
  • Clinical improvement persisted even after TPE was discontinued.

Findings:

  • Early initiation of TPE is associated with good outcomes in AP-induced MAHA-T.
  • The patient demonstrated stabilization and improvement following TPE, despite a normal ADAMTS13 level.
  • The value of TPE in altering the natural course of AP-induced MAHA-T requires further elucidation.

Implications:

  • This case highlights the potential benefit of TPE in managing acute pancreatitis-associated MAHA-T.
  • Further research is needed to clarify the role of ADAMTS13 testing in guiding treatment decisions.
  • Understanding the long-term impact and optimal duration of TPE is crucial for clinical practice.

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