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五例真性红细胞增多症与非肝硬化门静脉高压症的关联:病例系列

Association of polycythemia vera with non‑cirrhotic portal hypertension in five patients: A case series.

作者信息

Zhang Lili, Wang Yitong, Lv Wenliang, Hu Jianhua, Gou Chunyan

机构信息

Integrated Traditional Chinese and Western Medicine Center, Beijing You'an Hospital, Capital Medical University, Beijing 100069, P.R. China.

Department of Infectious Diseases, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, P.R. China.

出版信息

Exp Ther Med. 2023 Feb 16;25(4):149. doi: 10.3892/etm.2023.11848. eCollection 2023 Apr.

Abstract

Polycythemia vera (PV) and non-cirrhotic portal hypertension (NCPH) are relatively independent diseases, and few studies have linked them. However, in clinical settings, there may be a causal relationship. The aim of the present study was to analyze the clinical data of five patients with portal hypertension caused by PV and summarize the characteristics of PV with portal hypertension, to enhance the knowledge of this disease. The clinical data of five patients with PV and portal hypertension treated at Beijing You'an Hospital (Beijing, China) from January 2010 to March 2022 were retrospectively collected. The characteristics of these patients were then summarized and analyzed, including general information, laboratory tests, imaging and gastroscopy data. Overall, four patients were diagnosed with PV earlier compared with those with NCPH (ranging between days and years), whereas one patient was diagnosed with NCPH at the time of PV diagnosis. These four patients had blood cell elevations of 2-3 categories (red blood cells, white blood cells or platelets). The Child classification of liver functions in all five patients were found to be grades A-B. All five patients had splenomegaly, where three patients had portal vein thrombosis and cavernous degeneration. In addition, four patients had moderate or severe esophageal varices. In conclusion, to the best of our knowledge, this was the first case series of NCPH caused by PV. Among the patients, it was revealed that: i) NCPH caused by PV had milder liver function damage compared with cirrhosis-induced portal hypertension; ii) splenomegaly, ascites and esophageal varicose veins were prominent symptoms of NCPH caused by PV; iii) If PV is diagnosed, esophagogastroduodenoscopy should be performed as early as possible and regularly, where primary prevention measures for esophageal variceal hemorrhage are recommended; and iv) patients with PV with portal hypertension are at risk of thrombosis and bleeding, but it remains to be determined whether early antithrombotic therapy can reduce complications.

摘要

真性红细胞增多症(PV)和非肝硬化性门静脉高压症(NCPH)是相对独立的疾病,很少有研究将它们联系起来。然而,在临床环境中,它们可能存在因果关系。本研究的目的是分析5例由PV引起的门静脉高压患者的临床资料,总结PV合并门静脉高压的特征,以增进对该疾病的认识。回顾性收集了2010年1月至2022年3月在北京佑安医院(中国北京)接受治疗的5例PV合并门静脉高压患者的临床资料。然后对这些患者的特征进行了总结和分析,包括一般信息、实验室检查、影像学和胃镜检查数据。总体而言,与NCPH患者相比,4例患者更早被诊断为PV(间隔天数至数年),而1例患者在PV诊断时被诊断为NCPH。这4例患者有2 - 3类血细胞升高(红细胞、白细胞或血小板)。所有5例患者的肝功能Child分级均为A - B级。所有5例患者均有脾肿大,其中3例患者有门静脉血栓形成和海绵样变性。此外,4例患者有中度或重度食管静脉曲张。总之,据我们所知,这是首例由PV引起的NCPH病例系列。在这些患者中发现:i)与肝硬化引起的门静脉高压相比,PV引起的NCPH肝功能损害较轻;ii)脾肿大、腹水和食管静脉曲张是PV引起的NCPH的突出症状;iii)如果诊断为PV,应尽早并定期进行食管胃十二指肠镜检查,建议采取食管静脉曲张出血的一级预防措施;iv)PV合并门静脉高压的患者有血栓形成和出血的风险,但早期抗血栓治疗是否能减少并发症仍有待确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2224/9995705/08c861533cf1/etm-25-04-11848-g00.jpg

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