Delivery in a Patient with Paroxysmal Nocturnal Hemoglobinuria Successfully Managed with Low Molecular Weight Heparin Therapy. |
Ho Bin Kim, Hye Jin Chang, Jeong In Yang, Haeng Soo Kim, Hee Sug Ryu, Hyo Chul Kim |
1Department of Obstetrics and Gynecology, Ajou University School of Medicine, Suwon, Korea. 2Department of Hemato-Oncology, Ajou University School of Medicine, Suwon, Korea. |
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Abstract |
Paroxysmal nocturnal hemoglobinura is a very rare acquired clonal hematopoietic cell disorder leading to chronic intravascular hemolysis caused by abnormal complement activation. Pregnancy in a patient with paroxysmal nocturnal hemoglobinuria is often complicated with thrombosis resulting serious materno-fetal morbidity and mortality. A case of successful maintenance of the pregnancy, delivery and postpartum in a woman at gestational age of 37 weeks and 2 days with paroxysmal nocturnal hemoglobinuria managed with prophylactic transfusions and anticoagulation therapy by low molecular weight heparin is presented with a review of literature. |
Key Words:
Paroxysmal nocturnal hemoglobinuria, Low molecular weight heparin, Pregnancy |
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