Intrinsic Causes of Nonfibrotic Portal Hypertension-A Clinicopathologic Review of 56 Patients.

IF 0.9 4区 医学 Q4 PATHOLOGY
Hamza Ashmila, Nazia Khatoon, Andrew Keaveny, Muli Krishna, Raouf Nakhleh
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引用次数: 0

Abstract

Aim: The differential diagnosis of intrinsic nonfibrotic conditions that may lead to portal hypertension include hepatoportal sclerosis (HPS), nodular regenerative hyperplasia (NRH), and sinusoidal obstruction syndrome (SOS). In this article, we characterize the clinical features and outcome of these lesions when they manifest as portal hypertension. Methods: Data was collected through retrospective patient medical records. Results: Patients (HPS: 28, NRH: 17, SOS: 11) were identified more frequently in recent years. All groups presented with signs and symptoms of portal hypertension. All patients had complex medical histories. An elevated serum alkaline phosphatase occurred in all groups and an elevated bilirubin with SOS. Imaging of the liver with HPS and NRH suggested cirrhosis, which was not seen with SOS. 11%, 12%, and 9% of patients in the HPS, NRH, and SOS respectively, underwent transjugular intrahepatic portosystemic shunt placement to manage the complications of portal hypertension, while 43%, 24%, and 36% of patients respectively, received a liver transplant. Conclusions: Patients with HPS, NRH, and SOS had complex medical histories, likely contributing to the development of these lesions. They are recognized more frequently now. In contrast to HPS and NRH, SOS occurred in liver transplant recipients, was associated with elevated serum bilirubin, and imaging did not suggest the presence of advanced fibrosis/cirrhosis. Liver transplantation appeared to be a viable treatment for complications related to HPS and NRH. Retransplantation for SOS yielded mixed results. HPS, SOS, and NRH should be considered when evaluating liver specimens from patients with unexplained nonfibrotic portal hypertension. Key message: Intrinsic nonfibrotic causes of portal hypertension appear to be increasing in frequency. The differential diagnosis includes NRH, HPS, and SOS. These conditions are associated with complex diseases and possibly due to treatments. Pathologists need to be aware of this differential diagnosis when presented with liver biopsies performed to assess portal hypertension.

非纤维化门静脉高压症的内在原因--56 例患者的临床病理学回顾。
目的:可能导致门静脉高压的内在非纤维化病变的鉴别诊断包括肝门静脉硬化症(HPS)、结节性再生增生(NRH)和窦道阻塞综合征(SOS)。在本文中,我们将描述这些病变表现为门脉高压症时的临床特征和预后。研究方法通过回顾性病历收集数据。结果患者(HPS:28 例;NRH:17 例;SOS:11 例)的发病率近年来有所上升。所有组别均出现门静脉高压的体征和症状。所有患者都有复杂的病史。所有组别患者的血清碱性磷酸酶均升高,SOS患者的胆红素升高。HPS 和 NRH 的肝脏成像提示肝硬化,而 SOS 则未发现肝硬化。在 HPS、NRH 和 SOS 组中,分别有 11%、12% 和 9% 的患者接受了经颈静脉肝内门体分流术,以控制门脉高压并发症,而分别有 43%、24% 和 36% 的患者接受了肝移植。结论HPS、NRH 和 SOS 患者病史复杂,可能是导致这些病变发生的原因。现在,这些病变被更多人所认识。与HPS和NRH不同的是,SOS发生在肝移植受者身上,与血清胆红素升高有关,而且影像学检查并未提示存在晚期纤维化/肝硬化。肝移植似乎是治疗 HPS 和 NRH 相关并发症的一种可行方法。针对 SOS 的再移植结果不一。在评估不明原因的非纤维化门脉高压症患者的肝脏标本时,应考虑到HPS、SOS和NRH。关键信息:非纤维化性门脉高压的内在原因似乎越来越多。鉴别诊断包括 NRH、HPS 和 SOS。这些病症与复杂的疾病相关,也可能是由于治疗所致。病理学家在进行肝活检以评估门静脉高压时,需要注意这种鉴别诊断。
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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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
198
审稿时长
1 months
期刊介绍: International Journal of Surgical Pathology (IJSP) is a peer-reviewed journal published eight times a year, which offers original research and observations covering all major organ systems, timely reviews of new techniques and procedures, discussions of controversies in surgical pathology, case reports, and images in pathology. This journal is a member of the Committee on Publication Ethics (COPE).
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