Chinese General Practice ›› 2023, Vol. 26 ›› Issue (05): 641-646.DOI: 10.12114/j.issn.1007-9572.2022.0338

Special Issue: 胰腺炎最新文章合集

• Research of Typical Cases • Previous Articles    

Hereditary Pancreatitis in Children: Report of One Case with Pedigree Analysis and Literature Review

  

  1. 1. Department of Pediatrics, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China
    2. Department of Pediatrics, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning 530003, China
    3. Department of Radiology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China
    4. Department of Respiratory, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China
  • Received:2022-03-21 Revised:2022-05-31 Published:2023-02-15 Online:2022-06-16
  • Contact: SHAN Qingwen

儿童遗传性胰腺炎及其家系分析一例报道并文献复习

  

  1. 1.530021 广西壮族自治区南宁市,广西医科大学第一附属医院儿科
    2.530003 广西壮族自治区南宁市,广西壮族自治区妇幼保健院儿科
    3.530021 广西壮族自治区南宁市,广西医科大学第一附属医院放射科
    4.530021 广西壮族自治区南宁市,广西医科大学第一附属医院呼吸内科
  • 通讯作者: 单庆文
  • 作者简介:
    作者贡献:何小莉收集资料、撰写文章;梁淑恒、李妙遐提供部分资料;孔晋亮负责提供技术支持;单庆文进行写作指导,对文章内容进行审阅与修订。

Abstract:

Hereditary pancreatitis (HP) is a rare autosomal genetic disease that is often manifested by recurrent pancreatitis and complicated type 3c diabetes mellitus (T3cDM) , and even leads to pancreatic cancer, impairing the quality of life and prognosis of patients. We reported a child with HP caused by p.Val39Ala (V39A) mutation of the PRSS1 gene with a pedigree analysis, which is the first case report in China, hoping to provide clinicians with evidence for the diagnosis and treatment of HP.

Key words: Pancreatitis, Hereditary pancreatitis, Child, Serine proteases, Genes, Mutation, Type 3c diabetes mellitus, Pancreatic neoplasms

摘要:

遗传性胰腺炎(HP)是一种罕见的常染色体遗传病,表现为胰腺炎反复发作,常并发3c型糖尿病(T3cDM),甚至导致胰腺癌的发生,影响患者的生活质量及预后。本文报道了1例由丝氨酸蛋白酶1(PRSS1)基因p.Val39Ala(V39A)突变导致的HP患儿,同时对其家系进行了分析,以期为临床医师诊治HP提供参考。

关键词: 胰腺炎, 遗传性胰腺炎, 儿童, 丝氨酸蛋白酶类, 基因, 突变, 3c型糖尿病, 胰腺肿瘤