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肝嗜铬细胞瘤1例报告

王小磊 孟珊珊 曲丽梅 王广义 魏锋

引用本文:
Citation:

肝嗜铬细胞瘤1例报告

DOI: 10.3969/j.issn.1001-5256.2020.09.032
基金项目: 

吉林省科技发展计划项目国际科技合作项目(20190701008GH); 吉林大学白求恩计划(450060521279); 吉林大学第一医院交叉学创新研究专项(JDYYJCHX005); 

详细信息
  • 中图分类号: R735.7

A case of hepatic pheochromocytoma

Research funding: 

 

  • 摘要:

    <正>嗜铬细胞瘤是一种起源于肾上腺嗜铬细胞的神经内分泌肿瘤,它可以持续或间断分泌儿茶酚胺,包括去甲肾上腺素、多巴胺及肾上腺素。肾上腺外来源的嗜铬细胞瘤称为转移性嗜铬细胞瘤。嗜铬细胞瘤典型的临床表现有血压异常波动、心悸、头疼等,严重者可导致高血压危象,危及生命。本文报道了1例位于肝右后叶的嗜铬细胞瘤的青年患者,并讨论了临床表现、影像学表现、组织学病理和治疗方法。1病例资料

     

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    [11] ZHAO L,LIANG CZ. Progress in diagnosis and treatment of pheochromocytoma[J]. J Contem Urol Reprod Oncol,2019,11(3):181-183.(in Chinese)赵磊,梁朝朝.嗜铬细胞瘤的诊断及治疗进展[J].现代泌尿生殖肿瘤杂志,2019,11(3):181-183.
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  • 出版日期:  2020-09-20
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