[Budd-Chiari syndrome with fatal outcome in a patient with polycythemia vera and antiphospholipid antibody syndrome].

Gianpaolo Bragagni, Raffaele Brogna, Francesca Dazzani, Paola Franceschetti, Giorgio Zoli
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Abstract

We report the case of a 41-year-old woman, affected by Vaquez syndrome, admitted to our hospital for a severe pain in the right hypochondrium, suddenly followed by hepatomegaly and ascites. The clinical and laboratory data were suggestive of hepatic insufficiency and abdominal ultrasonography, integrated by color Doppler and computed tomography, revealed an interrupted hepatic venous outflow. In addition a spontaneous prolonged partial thromboplastin time was present and the patient was found to be positive for lupus anticoagulant. A transient clinical improvement, with a partial reperfusion of suprahepatic veins, was achieved with medical treatment by using anticoagulants, diuretics and paracentesis. However, the patient showed a subsequence of suprahepatic venous thrombosis, although two transjugular intrahepatic portosystemic shunts with stent placement and local thrombolysis were performed. The polycythemia vera is a disease mainly associated with Budd-Chiari syndrome but, in our patient, the thrombotic event occurred in spite of normal values of hematocrit and platelet count. Certainly in this case the lupus anticoagulant positivity represents an additional thrombogenic factor. Nowadays the antiphospholipid antibody syndrome is a recognized and not unusual cause of Budd-Chiari syndrome but, to our knowledge, this is the first case characterized by the presence of polycythemia vera and antiphospholipid antibody syndrome to be reported.

[真性红细胞增多症合并抗磷脂抗体综合征患者的Budd-Chiari综合征致死性结局]。
我们报告一例41岁的女性,患有Vaquez综合征,因右侧胁肋剧烈疼痛,突然出现肝肿大和腹水而入院。临床和实验室资料提示肝功能不全,腹部超声,结合彩色多普勒和计算机断层扫描,显示肝静脉流出中断。此外,自发性延长部分凝血活酶时间存在,患者被发现为狼疮抗凝剂阳性。通过使用抗凝剂、利尿剂和穿刺等药物治疗,出现了短暂的临床改善,肝上静脉部分再灌注。然而,患者随后出现肝上静脉血栓形成,尽管进行了两次经颈静脉肝内门体分流术并放置支架和局部溶栓。真性红细胞增多症是一种主要与Budd-Chiari综合征相关的疾病,但在本例患者中,尽管红细胞比容和血小板计数正常,但仍发生血栓形成事件。当然,在这种情况下,狼疮抗凝血阳性代表一个额外的血栓形成因素。目前,抗磷脂抗体综合征是一种公认的且并不罕见的Budd-Chiari综合征的病因,但据我们所知,这是第一例以真性红细胞增多症和抗磷脂抗体综合征为特征的病例报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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