| Literature DB >> 14663164 |
Costas Tsatalas1, Dimitris Margaritis, Despina Pantelidou, Ioannis Kotsianidis, Anastasios J Karayiannakis, Emanuel Spanoudakis, Zafiris Kartasis, Vasiliki Kaloutsi, Alexandros Polychronidis, Ioannis Manavis, George Bourikas.
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. Copyright 2003 S. Karger AG, BaselEntities:
Mesh:
Year: 2003 PMID: 14663164 DOI: 10.1159/000074224
Source DB: PubMed Journal: Acta Haematol ISSN: 0001-5792 Impact factor: 2.195