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遗传性蛋白C缺乏所致急性布加综合征中酷似浸润性肿块的肝坏死

Hepatic Necrosis Mimicking Infiltrative Masses in Acute Budd-Chiari Syndrome With Hereditary Protein C Deficiency.

作者信息

Ananchuensook Prooksa, Karuehardsuwan Julalak, Sanpawat Anapat, Wisedopas Naruemon, Treeprasertsuk Sombat, Komolmit Piyawat, Thanapirom Kessarin

机构信息

Division of Gastroenterology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Department of Pathology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

ACG Case Rep J. 2022 Jun 24;9(6):e00802. doi: 10.14309/crj.0000000000000802. eCollection 2022 Jun.

Abstract

We report the case of a patient with an unusual acute Budd-Chiari syndrome (BCS). The patient presented with high-grade fever and right upper quadrant pain. Infiltrative lesions at the right hepatic lobe and segment IVB with intrahepatic inferior vena cava and right hepatic vein thrombus appeared on abdominal imaging. Liver biopsy revealed hepatic infarction compatible with acute BCS. Thrombophilia work-up demonstrated low protein C activity with the -1657C/T mutation of the gene. Necrotic liver mass with acute BCS related to congenital protein C deficiency was diagnosed. Patient symptoms and necrotic masses improved after anticoagulant treatment for 4 months.

摘要

我们报告了一例患有罕见急性布加综合征(BCS)的患者。该患者表现为高热和右上腹疼痛。腹部影像学检查显示右肝叶和IVB段有浸润性病变,同时伴有肝内下腔静脉和右肝静脉血栓形成。肝活检显示肝梗死,符合急性布加综合征。血栓形成倾向检查显示蛋白C活性降低,伴有该基因的-1657C/T突变。诊断为与先天性蛋白C缺乏相关的急性布加综合征坏死性肝肿块。患者在接受抗凝治疗4个月后,症状和坏死肿块有所改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f7/9232359/77154f891f04/ac9-9-e00802-g001.jpg

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