open access

Vol 71, No 6 (2020)
Clinical vignette
Submitted: 2020-07-18
Accepted: 2020-08-28
Early publication date: 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
DOI: 10.5603/EP.a2020.0068
·
Pubmed: 33125697
·
Endokrynol Pol 2020;71(6):583-584.
Affiliations
  1. Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
  2. Excellence Center in Diabetes, Hormone, and Metabolism, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand
  3. Department of Medicine, Rayong Hospital, Rayong Province, Thailand
  4. Department of Radiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
  5. Department of Pathology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
  6. Department of Surgery, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand

open access

Vol 71, No 6 (2020)
Clinical Vignette
Submitted: 2020-07-18
Accepted: 2020-08-28
Early publication date: 2020-09-25

Abstract

Not required for Clinical Vignette.

Abstract

Not required for Clinical Vignette.

Get Citation

Keywords

organs of ZuckerKandl; paraganglioma; FH gene

About this article
Title

Paraganglioma of the organ of Zuckerkandl and FH gene mutation

Journal

Endokrynologia Polska

Issue

Vol 71, No 6 (2020)

Article type

Clinical vignette

Pages

583-584

Early publication date

2020-09-25

Page views

451

Article views/downloads

443

DOI

10.5603/EP.a2020.0068

Pubmed

33125697

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

References (5)
  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.

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