[A case of adult Gaucher's disease mainly initially manifested as hepatosplenomegaly]

Zhonghua Gan Zang Bing Za Zhi. 2024 Oct 20;32(10):940-942. doi: 10.3760/cma.j.cn501113-20240410-00192.
[Article in Chinese]

Abstract

戈谢病是一种溶酶体贮积病,因编码葡萄糖脑苷脂酶的基因突变,导致葡萄糖脑苷脂分解代谢途径受阻,其底物在肝、脾、骨骼、肺、甚至脑的巨噬细胞溶酶体中贮积,造成一系列器官受损。戈谢病是一种罕见的常染色体隐性遗传病,基因突变超400种。根据神经系统是否受累分为3种类型,其中I型最常见。现分享1例成人I型戈谢病的临床表现、诊断过程,提高对该病的认识。.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Gaucher Disease* / diagnosis
  • Hepatomegaly* / etiology
  • Humans
  • Male
  • Splenomegaly* / etiology