A Rare Case Presenting with Symptoms of Familial Pheochromacytoma

Cilt: 40 Sayı: 3 30 Eylül 2015
Mehtap Evran , Gamze Akkuş , Murat Sert , Tamer Tetiker
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A Rare Case Presenting with Symptoms of Familial Pheochromacytoma

Öz

Pheochromocytoma is a rare tumor in which seen an incidence of 1 per 100.000 in the general population. Pheochromocytoma is a catecholamine producing neuroendocrine tumor arising from adrenal medulla. A 46-year-old man experienced headache, sweating and palpitation referred to our hospital. Familial pheocromocytoma was detected. We presented this case as whole family members had suffered from morbidities and deaths due to this disorder

Anahtar Kelimeler

Pheocromocytoma, familial disorder, hypertension

Kaynakça

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  3. DeLellis R, Lloyd P, Heitz C. Pathology and Genetics of Tumours of Endocrine Organs (IARC WHO Classification of Tumours), IARC Press, 2004 Lyon, France. Martins R,
  4. Paragangliomas/Pheochromocytomas: Oriented Genetic Testing. Int J Endocrinol. 2014; 2014: 794187. doi: 10.1155/2014/794187. Epub 2014 May Bugalho MJ. Clinically
  5. Van Berkel A, Lenders JW, Timmers HJ. Diagnosis of endocrine pheochromocytoma and paraganglioma. Eur J Endocrinol. 2014;170:R109-119. diagnosis of
  6. Neumann HP, Bausch B, McWhinney SR, et al. Germ-line pheochromocytoma N Engl J Med. 2002;346:1459- in nonsyndromic
  7. Plouin PF, Duclos JM, Soppelsa F, et al Factors associated with perioperative morbidity and mortality in patients with pheochromocytoma: analysis of 165 operations at a single center J Clin Endocrinol Metab. 2001;86:1480-6.
  8. Maher ER, Eng. C. The pressure rises: update on the genetics of phaeochromocytoma Hum Mol Genet. 2002;11:2347-54. Ilias I, Pacak K. Current approaches and the recommended localization of pheochromocytoma J Clin Endocrinol Metab. 2004;89:479-91. for diagnostic
  9. Sahdev A, Sohaib A, Monson JP, et al CT and MR imaging of unusual locations of extra-adrenal paragangliomas (pheochromocytomas) Eur Radiol. 2005;15:85-92.
  10. Bauters C, Vantyghem MC, Leteurtre E, et al. Hereditary paragangliomas: a study of five susceptibility genes J Med Genet. 2003;40:e75. and

Ayrıntılar

Birincil Dil

İngilizce

Konular

-

Bölüm

-

Yazarlar

Gamze Akkuş Bu kişi benim

Murat Sert Bu kişi benim

Tamer Tetiker Bu kişi benim

Yayımlanma Tarihi

30 Eylül 2015

Gönderilme Tarihi

30 Eylül 2015

Kabul Tarihi

-

Yayımlandığı Sayı

Yıl 2015 Cilt: 40 Sayı: 3

DOI

https://doi.org/10.17826/cutf.81730

IZ

https://izlik.org/JA46BC63YL

Kaynak Göster

RIS / Bibtex
APA
Evran, M., Akkuş, G., Sert, M., & Tetiker, T. (2015). A Rare Case Presenting with Symptoms of Familial Pheochromacytoma. Cukurova Medical Journal, 40(3), 593-596. https://doi.org/10.17826/cutf.81730
AMA
1.Evran M, Akkuş G, Sert M, Tetiker T. A Rare Case Presenting with Symptoms of Familial Pheochromacytoma. Cukurova Med J. 2015;40(3):593-596. doi:10.17826/cutf.81730
Chicago
Evran, Mehtap, Gamze Akkuş, Murat Sert, ve Tamer Tetiker. 2015. “A Rare Case Presenting with Symptoms of Familial Pheochromacytoma”. Cukurova Medical Journal 40 (3): 593-96. https://doi.org/10.17826/cutf.81730.
EndNote
Evran M, Akkuş G, Sert M, Tetiker T (01 Ekim 2015) A Rare Case Presenting with Symptoms of Familial Pheochromacytoma. Cukurova Medical Journal 40 3 593–596.
IEEE
[1]M. Evran, G. Akkuş, M. Sert, ve T. Tetiker, “A Rare Case Presenting with Symptoms of Familial Pheochromacytoma”, Cukurova Med J, c. 40, sy 3, ss. 593–596, Eki. 2015, doi: 10.17826/cutf.81730.
ISNAD
Evran, Mehtap - Akkuş, Gamze - Sert, Murat - Tetiker, Tamer. “A Rare Case Presenting with Symptoms of Familial Pheochromacytoma”. Cukurova Medical Journal 40/3 (01 Ekim 2015): 593-596. https://doi.org/10.17826/cutf.81730.
JAMA
1.Evran M, Akkuş G, Sert M, Tetiker T. A Rare Case Presenting with Symptoms of Familial Pheochromacytoma. Cukurova Med J. 2015;40:593–596.
MLA
Evran, Mehtap, vd. “A Rare Case Presenting with Symptoms of Familial Pheochromacytoma”. Cukurova Medical Journal, c. 40, sy 3, Ekim 2015, ss. 593-6, doi:10.17826/cutf.81730.
Vancouver
1.Mehtap Evran, Gamze Akkuş, Murat Sert, Tamer Tetiker. A Rare Case Presenting with Symptoms of Familial Pheochromacytoma. Cukurova Med J. 01 Ekim 2015;40(3):593-6. doi:10.17826/cutf.81730
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