胰腺巨大副神经节瘤1例报告

徐洪基; 李鑫鑫; 刘凯

doi:10.3969/j.issn.1001-5256.2019.10.036

胰腺巨大副神经节瘤1例报告

DOI: 10.3969/j.issn.1001-5256.2019.10.036

1. 吉林大学第一医院肝胆胰外二科
2. 吉林大学第一医院放射线科

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中图分类号: R735.9
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出版历程
- 出版日期: 2019-10-20

A case of giant paraganglioma of the pancreas

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

摘要

摘要: <正>胰腺副神经节瘤是一种非常罕见的副神经节瘤,目前为止,文献报道不足35例[1]。副神经节瘤是一种起源于神经嵴细胞的罕见肿瘤[2]。其中恶性肿瘤占其中的1/10,而诊断为恶性肿瘤的患者5年生存率为50%。很多情况下,患者若未发现恶变的指标或者症状,该副神经节瘤可视为良性。手术治疗是该病的首选治疗措施,发现副神经节瘤后应尽早行手术切除治疗。1病例资料患者女性,50岁,自述近1年偶有上腹部疼痛不适,未重
- 胰腺肿瘤 /
- 副神经节瘤 /
- 胰十二指肠切除术
- pancreatic neoplasms /
- paraganglioma /
- pancreaticoduodenectomy

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参考文献(6)

[1] ERICKSON D,KUDVA YC,EBERSOLD MJ,et al. Benign paragangliomas:Clinical presentation and treatment outcomes in 236patients[J]. J Clin Endocrinol Metab,2001,86(11):5210-5216.

[2] KIMURA N,CAPELLA C,de KRIJGER RR,et al. Extra-adrenal sympathetic paraganglioma:Superior and inferior paraaortic[M]//DELELLIS RA,LIOYD RV,HEITZ PU,et al. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Endocrine Organs. Lyon,IARC Press,2004:164-165.

[3] ZENG ZP. Pheochromocytoma[M]. Clinical endocrinology,2011:637-644.(in Chinese)曾正陪.嗜铬细胞瘤[M].临床内分泌学,2011:637-644.

[4] GINESU GC,BARMINA M,PALIOGIANNIS P,et al. Nonfunctional paraganglioma of the head of the pancreas:A rare case report[J]. Int J Surg Case Rep,2016,28:81-84.

[5] SHUCH B,RICKETTS CJ,METWALLI AR,et al. The genetic basis of pheochromocytoma and paraganglioma:Implications for management[J]. Urology,2014,83(6):1225-1232.

[6] KIM SY,BYUN JH,CHOI G,et al. A case of primary paraganglioma that arose in the pancreas:The Color Doppler ultrasonography and dynamic CT features[J]. Korean J Radiol,2008,9(Suppl):s18-s21.

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