肝嗜铬细胞瘤1例报告

王小磊; 孟珊珊; 曲丽梅; 王广义; 魏锋

doi:10.3969/j.issn.1001-5256.2020.09.032

肝嗜铬细胞瘤1例报告

DOI: 10.3969/j.issn.1001-5256.2020.09.032

1. 吉林大学第一医院肝胆胰外一科
2. 吉林大学第一医院护理部
3. 吉林大学第一医院病理科

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
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出版历程
- 出版日期: 2020-09-20

A case of hepatic pheochromocytoma

First Department of Hepatopancreatobiliary Surgery, The First Hospital of Jilin University

Research funding:

摘要

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
- 嗜铬细胞瘤 /
- 肝肿瘤 /
- 肿瘤转移
- pheochromocytoma /
- liver neoplasms /
- neoplasm metastasis

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参考文献(11)

[1] LENDERS JW,DUH QY,EISENHOFER G,et al. Pheochromocytoma and paraganglioma:An endocrine society clinical practice guideline[J]. J Clin Endocrinol Metab,2014,99(6):1915-1942.

[2] HAMIDI O,YOUNG WF Jr,GRUBER L,et al. Outcomes of patients with metastatic phaeochromocytoma and paraganglioma:A systematic review and meta-analysis[J]. Clin Endocrinol(Oxf),2017,87(5):440-450.

[3] WANG QF,LIANG CZ,ZHU JS,et al. Diagnosis and treatment of pheochromocytoma in urinary bladder(One case report and literature review)[J]. J Contem Urol Reprod Oncol,2017,9(5):279-281.(in Chinese)汪群锋，梁朝朝，朱劲松，等．膀胱嗜铬细胞瘤1例诊治并文献复习[J]．现代泌尿生殖肿瘤杂志，2017,9(5):279-281.

[4] EISENHOFER G,PEITZSCH M. Laboratory evaluation of pheochromocytoma and paraganglioma[J]. Clin Chem,2014,60(12):1486-1499.

[5] PAPPACHAN JM,RASKAUSKIENE D,SRIRAMAN R,et al.Diagnosis and management of pheochromocytoma:A practical guide to clinicians[J]. Curr Hypertens Rep,2014,16(7):442.

[6] JACQUES AE,SAHDEV A,SANDRASAGARA M,et al. Adrenal phaeochromocytoma:Correlation of MRI appearances with histology and function[J]. Eur Radiol,2008,18(12):2885-2892.

[7] RAJA A,LEUNG K,STAMM M,et al. Multimodality imaging findings of pheochromocytoma with associated clinical and biochemical features in 53 patients with histologically confirmed tumors[J]. AJR Am J Roentgenol,2013,201(4):825-833.

[8] ADAM SZ,NIKOLAIDIS P,HOROWITZ JM,et al. Chemical shift MR imaging of the adrenal gland:Principles,pitfalls,and applications[J]. Radiographics,2016,36(2):414-432.

[9] JACQUES AE,SAHDEV A,SANDRASAGARA M,et al. Adrenal phaeochromocytoma:Correlation of MRI appearances with histology and function[J]. Eur Radiol,2008,18(12):2885-2892.

[10] NISHINO M,HAYAKAWA K,MINAMI M,et al. Primary retroperitoneal neoplasms:CT and MR imaging findings with anatomic and pathologic diagnostic clues[J]. Radiographics,2003,23(1):45-57.

[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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