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Journals / Çukurova Üniversitesi Tıp Fakültesi Dergisi / 2015 / Cilt: 40 - Sayı: 3

Familyal Feokromasitoma Semptomlarıyla Başvuran Nadir Bir Olgu

A Rare Case Presenting with Symptoms of Familial Pheochromacytoma

Murat SERT
Mehtap EVRAN
Tamer TETİKER
Gamze AKKUŞ
Pages
593–596
Publication Date
2022-10-10
DOI
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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.
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Key Findings & Data:A 46-year-old man experienced headache, sweating and palpitation referred to our hospital.
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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:Domain Parameters

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.

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Cite This Article

SERT, M., EVRAN, M., TETİKER, T., AKKUŞ, G. (2022). Familyal Feokromasitoma Semptomlarıyla Başvuran Nadir Bir Olgu. Çukurova Üniversitesi Tıp Fakültesi Dergisi, Cilt: 40 - Sayı: 3, 593–596. https://ajindex.com/articles/485862

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References (6)

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