Vol 71, No 6 (2020)
Clinical vignette
Published online: 2020-09-25

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Paraganglioma of the organ of Zuckerkandl and FH gene mutation

Thiti Snabboon12, Natnicha Houngngam2, Sirinrat Tangjittrong13, Kewalee Sasiwimonphan4, Kroonpong Iampenkhae5, Supparerk Prichayudhrichayudh6
Pubmed: 33125697
Endokrynol Pol 2020;71(6):583-584.


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  1. Lodish MB, Adams KT, Huynh TT, et al. Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of Zuckerkandl. Endocr Relat Cancer. 2010; 17(3): 581–588.
  2. Castro-Vega LJ, Buffet A, De Cubas AA, et al. Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas. Hum Mol Genet. 2014; 23(9): 2440–2446.
  3. Prichayudh S, Kritayakirana K, Snabboon T, et al. An extra-adrenal pheochromocytoma of the organ of Zuckerkandl: report of a case. J Med Assoc Thai. 2009; 92(11): 1532–1537.
  4. Lenders JWM, Duh QY, Eisenhofer G, et al. Endocrine Society. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2014; 99(6): 1915–1942.
  5. Clark GR, Sciacovelli M, Gaude E, et al. Germline FH mutations presenting with pheochromocytoma. J Clin Endocrinol Metab. 2014; 99(10): E2046–E2050.