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肝活检在不明原因门静脉高压病因诊断中的应用:门体静脉血管病变不容忽视。

Application of liver biopsy in etiological diagnosis of unexplained portal hypertension: Porto-sinusoidal vascular disease should not be ignored.

机构信息

Department of Medicine, Southeast University, Nanjing, China.

Department of Infectious and Liver Diseases, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.

出版信息

Medicine (Baltimore). 2024 Sep 27;103(39):e39819. doi: 10.1097/MD.0000000000039819.

Abstract

The diagnostic value of liver biopsy has been confirmed in patients with abnormal liver test results; however, little data are available on its application in patients with portal hypertension. This study aimed to investigate the utility of liver biopsy for the etiological diagnosis of unexplained portal hypertension, and explore the clinical and pathological characteristics of each etiology. A retrospective observational analysis was conducted on 1367 patients who underwent liver biopsy at the Second Hospital of Nanjing from 2017 to 2019. Of these, 188 patients with unexplained portal hypertension were enrolled. The clinical and pathological characteristics were collected and reassessed in a multidisciplinary team meeting. Among these patients, 174 (92.6%, 174/188) had a definite etiological diagnosis through liver biopsy. The main etiologies were autoimmune hepatitis in 47 patients (25%, 47/188), autoimmune hepatitis-primary biliary cirrhosis overlap syndrome in 41 patients (21.8%, 41/188), and porto-sinusoidal vascular disease (PSVD) in 40 patients (21.3%, 40/188). Compared to liver cirrhosis, PSVD patients were younger and the liver function damage of which was subtler. The widths of portal vein diameter were widest in PSVD but the liver stiffness measurement were almost normal. Splenomegaly was common in PSVD, but ascites were less frequent than in autoimmune hepatitis (25.0% vs 51.1%, P = .013). Based on the histological patterns, we found that cholestatic liver diseases such as primary biliary cirrhosis, autoimmune hepatitis-primary biliary cirrhosis overlap syndrome, and progressive familial intrahepatic cholestasis could lead to non-cirrhotic portal hypertension, while vascular liver diseases such as PSVD and Budd-Chiari syndrome could also show fibrous proliferation as the disease progresses. Liver biopsy is safe and valuable for etiological diagnosis of unexplained portal hypertension. Cirrhosis is the leading cause of portal hypertension, and porto-sinusoidal vascular diseases should also be considered. Clinical features may be helpful in suggesting the cause; however, pathological examination is still indispensable for disease diagnosis and progression assessment.

摘要

肝活检在肝功能异常患者中的诊断价值已得到证实;然而,关于其在门脉高压患者中的应用,数据有限。本研究旨在探讨肝活检在不明原因门脉高压病因诊断中的作用,并探讨各病因的临床和病理特征。对 2017 年至 2019 年在南京第二医院行肝活检的 1367 例患者进行回顾性观察性分析,其中 188 例为不明原因门脉高压患者。通过多学科团队会议收集并重新评估临床和病理特征。在这些患者中,174 例(92.6%,174/188)通过肝活检明确病因诊断。主要病因包括自身免疫性肝炎 47 例(25%,47/188)、自身免疫性肝炎-原发性胆汁性胆管炎重叠综合征 41 例(21.8%,41/188)和窦前性门脉高压(PSVD)40 例(21.3%,40/188)。与肝硬化相比,PSVD 患者更年轻,肝功能损害更轻微。PSVD 患者的门静脉直径最宽,而肝硬度测量值几乎正常。脾肿大在 PSVD 中很常见,但腹水较自身免疫性肝炎少见(25.0%比 51.1%,P=0.013)。根据组织学模式,我们发现原发性胆汁性胆管炎、自身免疫性肝炎-原发性胆汁性胆管炎重叠综合征和进行性家族性肝内胆汁淤积症等胆汁淤积性肝病可导致非肝硬化性门脉高压,而 PSVD 和布加综合征等血管性肝病在疾病进展时也可表现出纤维增生。肝活检对于不明原因门脉高压的病因诊断是安全且有价值的。肝硬化是门脉高压的主要原因,也应考虑门脉窦前血管疾病。临床特征有助于提示病因;然而,病理检查对于疾病诊断和进展评估仍然不可或缺。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382e/11441879/50eaa7df6b32/medi-103-e39819-g001.jpg

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