中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 35 Issue 10
Oct.  2019
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A case of giant paraganglioma of the pancreas

DOI: 10.3969/j.issn.1001-5256.2019.10.036
  • Published Date: 2019-10-20
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  • [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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