Magnan Heather, Kayton Mark L, DiMichele Donna M, Araten David J, Kernan Nancy A, Boulad Farid
Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.
Pediatr Blood Cancer. 2009 Sep;53(3):472-4. doi: 10.1002/pbc.22058.
We describe a patient with paroxysmal nocturnal hemoglobinuria (PNH) and no previous history of thrombosis who presented with hepatic venous thromboses and subsequently developed splenic infarction and rupture requiring splenectomy while on anticoagulation therapy for the hepatic thromboses. The patient's anticoagulation was complicated by heparin-induced thrombocytopenia (HIT) highlighting the unique management challenge presented by PNH in combination with HIT.
我们描述了一名阵发性夜间血红蛋白尿(PNH)患者,其既往无血栓形成病史,出现肝静脉血栓形成,随后在接受肝血栓抗凝治疗期间发生脾梗死和破裂,需要进行脾切除术。患者的抗凝治疗因肝素诱导的血小板减少症(HIT)而复杂化,突出了PNH合并HIT所带来的独特管理挑战。