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多形性肉瘤压迫下腔静脉导致布加综合征:一例报告

Budd-Chiari syndrome from pleomorphic sarcoma compressing the inferior vena cava: A case report.

作者信息

Camp Brandon, Danza Clifford N, Fateri Cameron, Sun Shawn, Phillipi Michael, Houshyar Roozbeh

机构信息

Department of Radiological Sciences, University of California, Irvine, CA 92868-3201, USA.

出版信息

Radiol Case Rep. 2025 Jul 26;20(10):5161-5164. doi: 10.1016/j.radcr.2025.06.081. eCollection 2025 Oct.

Abstract

Budd-Chiari syndrome is a rare condition characterized by obstruction of the hepatic veins or inferior vena cava, leading to portal hypertension and liver dysfunction. While common etiologies include thrombosis or malignancy, we present, to our knowledge, the first reported case in the English-language literature of Budd-Chiari syndrome secondary to metastatic undifferentiated pleomorphic sarcoma. A 52-year-old male with an extensive history of metastatic undifferentiated pleomorphic sarcoma presented with a 10-day history of vomiting and abdominal pain. A contrast-enhanced computed tomography scan of the abdomen revealed a large mediastinal mass representing likely further metastasis compressing the suprahepatic inferior vena cava, resulting in severe congestive hepatopathy consistent with Budd-Chiari syndrome. While hepatocellular carcinoma, renal cell carcinoma, leiomyosarcoma, and other malignancies have been linked to Budd-Chiari syndrome, this report highlights a novel cause. In cases of Budd-Chiari syndrome secondary to malignancy, vessel obstruction may result from compression, infiltration, or bland thrombus formation.

摘要

布加综合征是一种罕见的疾病,其特征为肝静脉或下腔静脉阻塞,导致门静脉高压和肝功能障碍。常见病因包括血栓形成或恶性肿瘤,据我们所知,我们报告了英文文献中首例继发于转移性未分化多形性肉瘤的布加综合征病例。一名有广泛转移性未分化多形性肉瘤病史的52岁男性,出现了10天的呕吐和腹痛症状。腹部增强计算机断层扫描显示,一个巨大的纵隔肿块可能代表进一步转移,压迫肝上下腔静脉,导致与布加综合征相符的严重充血性肝病。虽然肝细胞癌、肾细胞癌、平滑肌肉瘤和其他恶性肿瘤与布加综合征有关,但本报告强调了一个新的病因。在继发于恶性肿瘤的布加综合征病例中,血管阻塞可能是由于压迫、浸润或单纯血栓形成所致。

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