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A Case of Acute Budd-Chiari Syndrome Complicating Primary Antiphospholipid Syndrome Presenting as Acute Abdomen and Responding to Tight Anticoagulant Therapy

机译:急性腹部布氏综合征合并原发性抗磷脂综合征表现为急性腹部对严格的抗凝治疗有反应

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摘要

A 34-year-old woman with primary antiphospholipid syndrome was admitted to the Gastroenterology Department of our hospital with fever, acute abdomen, watery diarrhea, and extremely high levels of inflammatory parameters. She had a history of left lower limb deep vein thrombosis and pulmonary embolism and was taking warfarin potassium. Acute gastroenteritis was suspected and an antibiotic was administered, but symptoms progressed. Abdominal ultrasonography showed occlusion of the left hepatic vein and the middle hepatic vein and her D-dimer level was high. Accordingly, Budd-Chiari syndrome was diagnosed and high-dose intravenous infusion of heparin was initiated. Her abdominal symptoms improved and the levels of inflammatory parameters and D-dimer decreased rapidly. It is known that antiphospholipid syndrome can be complicated by Budd-Chiari syndrome that usually occurs as subacute or chronic onset, but acute onset is rare. It is difficult to diagnose acute Budd-Chiari syndrome complicating antiphospholipid syndrome and this complication generally has a poor outcome. However, the present case can get early diagnosis and successful treatment with tight anticoagulant therapy.
机译:一名34岁的原发性抗磷脂综合征的妇女因发热,急腹症,水样腹泻和极高的炎症指标被收治到我院消化内科。她有左下肢深静脉血栓形成和肺栓塞的病史,正在服用华法林钾盐。怀疑患有急性肠胃炎并使用了抗生素,但症状有所发展。腹部超声检查显示左肝静脉和肝中静脉闭塞,D-二聚体水平高。因此,诊断出Budd-Chiari综合征并开始大剂量静脉内输注肝素。她的腹部症状得到改善,炎症参数和D-二聚体水平迅速下降。众所周知,抗磷脂综合征可以并发于通常为亚急性或慢性发作的Budd-Chiari综合征,但很少有急性发作。难以诊断出合并有抗磷脂综合征的急性Budd-Chiari综合征,而且这种并发症通常预后较差。但是,本例可以通过严格的抗凝治疗得到早期诊断并成功治疗。

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