A case of congenital prothrombin deficiency and idiopathic thrombocytopenic purpura in a pregnant female

Hereditary prothrombin deficiency is an autosomal recessive disorder with an estimated incidence of 1 in 2 million [1]. Presentation of the disease is variable; however, it is usually associated with moderate to severe bleeding tendencies including muscle hematomas, hemarthrosis, intracranial, mucos...

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Veröffentlicht in:Blood coagulation & fibrinolysis 2017-01, Vol.28 (1), p.100-101
Hauptverfasser: Harel, Ronen, Shani, Dana, Donohoe, Kelsey
Format: Artikel
Sprache:eng
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Zusammenfassung:Hereditary prothrombin deficiency is an autosomal recessive disorder with an estimated incidence of 1 in 2 million [1]. Presentation of the disease is variable; however, it is usually associated with moderate to severe bleeding tendencies including muscle hematomas, hemarthrosis, intracranial, mucosal, and postoperative bleeding. Here we report a case of a 35-year-old pregnant woman with congenital hypoprothrombinemia and idiopathic thrombocytopenic purpura, review the literature, and discuss its epidemiology, presentation, diagnosis, and treatment.
ISSN:0957-5235
1473-5733
DOI:10.1097/MBC.0000000000000534