Thrombotic microangiopathy as a complication of acute pancreatitis

Authors

  • Bruno Scarlatto Universidad de la República, Facultad de Medicina, Hospital de Clínicas, Cátedra de Medicina Intensiva, Asistente. Médico Intensivista. MUCAM, Unidad de Medicina Intensiva, Médico de staff
  • Sofía Kohn Universidad de la República, Facultad de Medicina, Hospital de Clínicas, Cátedra de Medicina Intensiva, Medicina Intensiva, Residente
  • William Manzanares Universidad de la República, Facultad de Medicina, Hospital de Clínicas, Cátedra de Medicina Intensiva, Profesor Titular. Médico Intensivista. MUCAM, Unidad de Medicina Intensiva, Director

DOI:

https://doi.org/10.29193/RMU.38.4.11

Keywords:

ACUTE PANCREATITIS, THROMBOTIC THROMBOCYTOPENIC PURPURA

Abstract

Thrombotic thrombocytopenic purpura is rather an unusual thrombotic microangiopathy characterized by hemolytic anemia and plateletopenia which results in high morbimortality rates. The most frequent form of this disease is immune thrombotic thrombocytopenic purpura, also known as acquired thrombotic thrombocytopenic purpura, which is caused by enzime deficiency disintegrin-like and metalloprotease with thrombospondin type 1 motif 13 (ADAMTS13) that is secondary to antibodies in plasma. The study presents the case of a patient with a diagnosis of acute pancreatitis with a rare complication of thrombotic thrombocytopenic purpura which is exceptional in the clinical practice.

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Published

2022-12-20

How to Cite

1.
Scarlatto B, Kohn S, Manzanares W. Thrombotic microangiopathy as a complication of acute pancreatitis. Rev. Méd. Urug. [Internet]. 2022 Dec. 20 [cited 2024 Sep. 16];38(4):e38412. Available from: https://revista.rmu.org.uy/index.php/rmu/article/view/988