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在一名伪装成肝细胞癌的乙肝核心总抗体阳性患者中检测到的肝脏病变:肝紫癜症1例罕见病例及文献复习

Liver lesions detected in a hepatitis B core total antibody-positive patient masquerading as hepatocellular carcinoma: a rare case of peliosis hepatis and a review of the literature.

作者信息

Tan Chun Han Nigel, Soon Gwyneth Shook Ting, Kow Wei Chieh Alfred

机构信息

Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, University Surgical Cluster, National University Health System, Singapore.

Department of Pathology, National University Health System, Singapore.

出版信息

Ann Hepatobiliary Pancreat Surg. 2017 Aug;21(3):157-162. doi: 10.14701/ahbps.2017.21.3.157. Epub 2017 Aug 31.

Abstract

Peliosis Hepatis (PH) is a rare vascular disorder of the liver, characterized by the presence of cystic blood-filled cavities distributed throughout the hepatic parenchyma. The pathogenesis of PH remains controversial. The preoperative diagnosis of PH is difficult, due to the non-specific imaging characteristics of PH and almost all cases are diagnosed on histology post resection. This study presents a case of PH masquerading as hepatocellular carcinoma (HCC). The patient is a 45-year old Chinese lady, who presented with transaminitis. She was found to be hepatitis B virus core total antibody-positive with an alpha-fetoprotein (AFP) of 29.4 ng/ml. Triphasic liver computed tomography showed several arterial hypervascular lesions and hypoenhancing lesions on the venous phase, particularly in the segments 6/7. Subsequently, a magnetic resonance imaging scan showed multiple lesions in the right hemiliver with an indeterminate enhancement patterns. Subsequently, she decided to undergo a resection procedure. Histopathology revealed findings consistent with PH with some unusual features. This case demonstrates a clinical conundrum, in which PH presented with a raised AFP, in a patient with risk factors for the development of HCC. The clinical suspicion of PH should be high in patients, who present with multiple hepatic lesions with variable enhancement patterns.

摘要

肝紫癜病(PH)是一种罕见的肝脏血管疾病,其特征是在整个肝实质内存在充满血液的囊性腔隙。PH的发病机制仍存在争议。由于PH的影像学特征不具特异性,PH的术前诊断较为困难,几乎所有病例都是在切除术后通过组织学诊断的。本研究报告了一例伪装成肝细胞癌(HCC)的PH病例。患者是一位45岁的中国女性,因转氨酶升高就诊。她的乙肝病毒核心总抗体呈阳性,甲胎蛋白(AFP)为29.4 ng/ml。肝脏三期计算机断层扫描显示有几个动脉期高血供病变,静脉期呈低密度强化病变,特别是在6/7段。随后,磁共振成像扫描显示右半肝有多个病变,强化方式不确定。随后,她决定接受切除手术。组织病理学检查结果符合PH,但有一些不寻常的特征。该病例显示了一个临床难题,即PH在有HCC发生风险因素的患者中表现为AFP升高。对于出现多个强化方式各异的肝脏病变的患者,临床上应高度怀疑PH。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1bd/5620477/2f78de6d3873/ahbps-21-157-g001.jpg

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