鼻窦港血管病和下坡静脉曲张:不同的临床实体?

Inês Pestana, C. Noronha Ferreira, Rita Luís, Rui Sousa, Eduardo Abrantes Pereira, A. Banhudo
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摘要

简介门-鼻窦血管病(PSVD)是一种实体病,其特点是不存在组织学上的肝硬化,而且无论是否存在门静脉高压症(PHT),都能检测到特异性或非特异性的组织学结果。目前对其发病机理仍知之甚少。肺动脉高压(PAH)与门静脉高压(PHT)无关,可能与中心静脉压升高有关,而中心静脉压升高在极少数情况下会导致食管近端出现下坡静脉曲张。病例介绍:一名 53 岁的女性,病史和药史均无异常,3 天前出现血便、上腹痛和吐血。体格检查发现双侧腿部周围水肿。实验室检查结果包括严重贫血、肝酶学正常、NT-proBNP 1 748 pg/mL。内镜检查显示食管近端大静脉曲张和轻度高血压性胃病。肝病病因全套检查结果为阴性。超声波检查显示肝脏表面不规则、脾脏肿大、肝上静脉和下腔静脉扩张。超声心动图显示心脏瓣膜和腔室明显异常,尤其是右侧,以及中重度 PAH。开始使用利尿剂治疗后,临床症状有所改善。由于不耐受,β-受体阻滞剂被暂停使用。血管造影检查未发现门静脉侧支。内镜复查显示食管静脉曲张较大,但已缩小,无红点。心肺血液动力学评估显示,患者为中度 PAH(40 毫米汞柱)。肝脏血液动力学检查显示,该患者无临床意义的窦状 PHT。经颈静脉肝活检发现结节性再生增生,提示为 PSVD。讨论/结论:该病例病情复杂,诊断困难,说明了 PSVD 和门静脉肺动脉高压之间的关联并不多见,经颈静脉肝活检和压力测量对确诊这两种疾病非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Porto-Sinusoidal Vascular Disease and Downhill Varices: Separate Clinical Entities?
Introduction: Porto-sinusoidal vascular disease (PSVD) is an entity characterized by the absence of histologic liver cirrhosis and the detection of specific or non-specific histological findings, irrespective of the presence of portal hypertension (PHT). The pathogenesis remains poorly understood. Pulmonary arterial hypertension (PAH), independently of the presence of PHT, can be associated with an increase in central venous pressure, which can rarely lead to the development of downhill varices in the proximal esophagus. Case Presentation: A 53-year-old woman, with an unremarkable medical and pharmacological history, presented with a 3-day history of melena, epigastric pain and hematemesis. Physical examination revealed bilateral peripheral edema of the legs. Laboratory findings included severe anemia, normal hepatic enzymology, and NT-proBNP 1,748 pg/mL. Endoscopy showed large proximal esophageal varices and mild hypertensive gastropathy. A complete liver disease etiology panel was negative. Ultrasound showed an irregular liver surface, splenomegaly, and dilated supra-hepatic veins and inferior vena cava. Echocardiogram revealed significant cardiac valve and cavity abnormalities, especially on the right side, as well as moderate to severe PAH. Diuretics therapy was started with clinical improvement. Beta-blockers were suspended due to intolerance. There were no images suggestive of portosystemic collateralization on angiography. Re-evaluation endoscopy showed large but reduced esophageal varices, without red spots. Cardiopulmonary hemodynamic assessment revealed moderate PAH (40 mm Hg). Liver hemodynamic study revealed non-clinically significant sinusoidal PHT. Transjugular liver biopsy revealed nodular regenerative hyperplasia suggestive of PSVD. Discussion/Conclusion: The case was complex and presented diagnostic challenges, illustrating the uncommonly reported association between PSVD and porto-pulmonary hypertension and the importance of the transjugular liver biopsy and pressure measurements to confirm both diagnoses.
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