SavedAdd your journal

Journals / Cukurova Medical Journal / 2015 / Cilt: 40 - Sayı: 3

A Rare Case Presenting with Symptoms of Familial Pheochromacytoma

Familyal Feokromasitoma Semptomlarıyla Başvuran Nadir Bir Olgu

Mehtap EVRAN
Gamze AKKUŞ
Murat SERT
Tamer TETİKER
Pages
593–596
Publication Date
2015-09-30
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We presented this case as whole family members had suffered from morbidities and deaths due to this disorder

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Pheochromocytoma is a rare tumor in which seen an incidence of 1 per 100.000 in the general population.
📊
Key Findings & Data:A 46-year-old man experienced headache, sweating and palpitation referred to our hospital.
💡
Conclusion & Impact:We presented this case as whole family members had suffered from morbidities and deaths due to this disorder
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Pheocromocytoma · familial disorder · hypertension

Abstract

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

Özet

Feokromasitoma 100.000 kişide bir görülebilen nadir tümörlerden birisidir. Genel olarak adrenal medulladan katekolamin salınımı ile karakterizedir. Kırk altı yaşında erkek hasta baş ağrısı, terleme, çarpıntı şikayeti ile kliniğimize başvurdu. Hastaya feokromasitoma tanısı konuldu. Bu yazıda ailesinde feokromasitomaya bağlı morbidite ve ölüm öyküsü olan bir hasta aktarılmıştır.

🔖

Cite This Article

EVRAN, M., AKKUŞ, G., SERT, M., TETİKER, T. (2015). A Rare Case Presenting with Symptoms of Familial Pheochromacytoma. Cukurova Medical Journal, Cilt: 40 - Sayı: 3, 593–596. https://ajindex.com/articles/213521

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (6)

  1. Santos P, Pimenta T, Taveira-Gomes A. Hereditary pheochromocytoma. Int J Surg Pathol. 2014;22:393- 400 Kaltsas GA, Papadogias D, Grossman AB. The clinical presentation (symptoms and signs) of sporadic and familial chromaffin cell tumours (phaeochromocytomas and paragangliomas) Front Horm Res. 2004;31:61-75.
  2. DeLellis R, Lloyd P, Heitz C. Pathology and Genetics of Tumours of Endocrine Organs (IARC WHO Classification of Tumours), IARC Press, 2004
  3. Lyon, France. Martins R, Paragangliomas/Pheochromocytomas: Oriented Genetic Testing. Int J Endocrinol. 2014; 2014: 794187. doi: 10.1155/2014/794187. Epub 2014 May Bugalho MJ. Clinically Van Berkel A, Lenders JW, Timmers HJ. Diagnosis of endocrine pheochromocytoma and paraganglioma. Eur J Endocrinol. 2014;170:R109-119. diagnosis of Neumann HP, Bausch B, McWhinney SR, et al. Germ-line pheochromocytoma N Engl J Med. 2002;346:1459- in nonsyndromic 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.
  4. Maher ER, Eng. C. The pressure rises: update on the genetics of phaeochromocytoma Hum Mol Genet. 2002;11:2347-54.
  5. Ilias I, Pacak K. Current approaches and the recommended localization of pheochromocytoma J Clin Endocrinol Metab. 2004;89:479-91. for diagnostic 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.
  6. Bauters C, Vantyghem MC, Leteurtre E, et al. Hereditary paragangliomas: a study of five susceptibility genes J Med Genet. 2003;40:e75. and