Splenectomy for massive splenic infarction unmasks paroxysmal nocturnal hemoglobinuria

Acta Haematol. 2003;110(4):193-6. doi: 10.1159/000074224.

Abstract

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disorder characterized by pancytopenia, hemolysis, and thrombosis. Abdominal vein thrombosis is a life-threatening manifestation of this disease. We present a patient with complete spleen necrosis due to thrombosis of the splenic vessels. After splenectomy, other causes of thrombophilia were excluded and the diagnosis of PNH was established. The patient was put on anticoagulation but despite the prophylactic international normalized ratio maintained over the last 18 months of follow-up, he had another episode of intrahepatic thrombosis which was treated with tissue plasminogen activator thrombolysis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Hemoglobinuria, Paroxysmal / complications
  • Hemoglobinuria, Paroxysmal / diagnosis*
  • Humans
  • Male
  • Splenectomy*
  • Splenic Infarction / complications
  • Splenic Infarction / diagnostic imaging
  • Splenic Infarction / surgery*
  • Tomography, X-Ray Computed