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Paraganglioma of the organ of Zuckerkandl and FH gene mutation
- Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
- Excellence Center in Diabetes, Hormone, and Metabolism, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand
- Department of Medicine, Rayong Hospital, Rayong Province, Thailand
- Department of Radiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
- Department of Pathology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
- Department of Surgery, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
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Abstract
Not required for Clinical Vignette.
Abstract
Not required for Clinical Vignette.
Keywords
organs of ZuckerKandl; paraganglioma; FH gene
Title
Paraganglioma of the organ of Zuckerkandl and FH gene mutation
Journal
Issue
Article type
Clinical vignette
Pages
583-584
Published online
2020-09-25
Page views
738
Article views/downloads
720
DOI
Pubmed
Bibliographic record
Endokrynol Pol 2020;71(6):583-584.
Keywords
organs of ZuckerKandl
paraganglioma
FH gene
Authors
Thiti Snabboon
Natnicha Houngngam
Sirinrat Tangjittrong
Kewalee Sasiwimonphan
Kroonpong Iampenkhae
Supparerk Prichayudhrichayudh
- 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.
- 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.
- 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.
- 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.
- Clark GR, Sciacovelli M, Gaude E, et al. Germline FH mutations presenting with pheochromocytoma. J Clin Endocrinol Metab. 2014; 99(10): E2046–E2050.