实用肝脏病杂志 ›› 2023, Vol. 26 ›› Issue (2): 230-233.doi: 10.3969/j.issn.1672-5069.2023.02.020

• 自身免疫性肝病 • 上一篇    下一篇

系统性硬化病合并原发性胆汁性胆管炎并发门静脉高压症12例临床特点分析*

张丽丽, 张纯, 王一同, 勾春燕, 胡建华, 吕文良   

  1. 100053 北京市 中国中医科学院广安门医院感染性疾病科(张丽丽,吕文良);首都医科大学附属北京佑安医院中西医结合中心(张丽丽,张纯,王一同,勾春燕,胡建华)
  • 收稿日期:2022-09-01 出版日期:2023-03-10 发布日期:2023-03-21
  • 通讯作者: 吕文良,E-mail:lvwenliang@sohu.com
  • 作者简介:张丽丽,女,29岁,博士研究生
  • 基金资助:
    *北京市扬帆计划重点医学专业-中西医结合重症肝病研究项目(编号:ZYLX201819);中国中医科学院科技创新工程项目(编号:CI2021A00801/CI2021A00802)

Clinical characteristics of systemic sclerosis complicated with primary biliary cholangitis and portal hypertension: Analysis of 12 cases

Zhang Lili, Zhang Chun, Wang Yitong, et al.   

  1. Department of Infectious Diseases, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, China
  • Received:2022-09-01 Online:2023-03-10 Published:2023-03-21

摘要: 目的 总结分析系统性硬化病(SSc)合并原发性胆汁性胆管炎(PBC)并发门静脉高压症患者的临床特征。方法 2010年1月~2022年3月于首都医科大学附属北京佑安医院住院的SSc合并PBC并发门静脉高压症患者12例,分析其临床表现、实验室、腹部影像学和胃镜检查等临床资料。结果 5例患者因呕血和/或黑便为首发症状就诊;8例患者SSc诊断早于PBC诊断;10例患者血红蛋白(HGB)下降,9例PLT下降,8例GGT和ALP升高,表现出胆汁淤积现象;10例患者具有电子胃镜检查结果,提示均存在食管静脉曲张;CT/超声检查提示均有脾肿大,8例提示有侧支循环形成,9例有腹水。结论 SSc合并PBC并发门静脉高压症患者临床表现与PBC患者相似,门静脉高压症表现较为明显,胆汁淤积较转氨酶升高更为明显,在诊断SSc后应积极完善PBC诊断的相关检查,早期诊断,早期干预,可能会进一步改善疾病的不良结局。

关键词: 原发性胆汁性胆管炎, 系统性硬化病, 硬皮病, 消化道出血, 食管静脉曲张

Abstract: Objective This paper aimed too summarize the clinical characteristics of patients with systemic sclerosis (SSc) complicated with primary biliary cholangitis (PBC) and portal hypertension. Methods Twelve patients with SSc complicated with PBC and portal hypertension were hospitalized in Beijing You'an Hospital Affiliated to Capital Medical University between January 2010 and March 2022, and the clinical symptoms, laboratory tests, abdominal imaging and gastroscopy data were analyzed. Results Among the 12 patients, 5 patients went to see doctors for hematemesis and/or melena as the first symptom; 8 patients were diagnosed with SSc earlier than PBC; 10 patients had decreased peripheral blood hemoglobin (HGB) levels, and 9 patients had decreased blood PLT counts; 8 patients had elevated serum GGT and ALP levels, showing cholestasis; 10 patients had electronic gastroscopic findings, suggesting esophageal varices, 12 patients had splenomegaly by CT/ultrasonography, and 9 patients had varying degrees of ascites, 8 patients had formation of collateral circulation. Conclusion The clinical manifestations of patients with SSc, PBC and portal hypertension are similar to patients with PBC alone. The clinical manifestations of portal hypertension are more obvious, and the cholestasis is more obvious than the increase of serum transaminases levles. It might be necessary to actively find PBC, when the SSc is diagnosed. Early diagnosis and early intervention might improve the outcome of patients with those entities.

Key words: Primary biliary cholangitis, Systemic sclerosis, Scleroderma, Gastrointestinal bleeding, Esophageal varices