Journals / Şişli Etfal Hastanesi Tıp Bülteni / 2009 / Cilt: 43 - Sayı: 1

2 cases of hereditary pheochromositoma

İki olgu nedeniyle kalıtsal feokromasitoma

Pages
48–50
DOI
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AI Summary & Key Takeaways

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

In this study we present two peadiatric siblings cases of hereditary pheochromositoma and discuss their anesthesia characteristics.

📌 3 Key Takeaways

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Objective & Hypothesis:Pheochromositoma is a rare tumor seen generally in middle aged group patients.
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Key Findings & Data:This tumor is generally bilateral and much more rarely seen in peadiatric patients.
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Conclusion & Impact:In this study we present two peadiatric siblings cases of hereditary pheochromositoma and discuss their anesthesia characteristics.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Ergen · Çocuk · Kadın

Abstract

Pheochromositoma is a rare tumor seen generally in middle aged group patients. This tumor is generally bilateral and much more rarely seen in peadiatric patients. In this study we present two peadiatric siblings cases of hereditary pheochromositoma and discuss their anesthesia characteristics.

Özet

Feokromasitoma, genellikle orta yaş grubunda görülen ender bir tümördür. Pediatrik olgularda ise daha da nadir ve genellikle bilateraldir. Bu çalışmada iki kardeş çocuk olgu üzerinden kalıtsal feokromasitomada anestezi özellikleri tartışıldı.

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Cite This Article

OBA, S., PAKSOY, İ., GÜNDOĞAN, F., ÇINAR, S., ÖZBAĞRIAÇIK, Ö. (2009). 2 cases of hereditary pheochromositoma. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 43 - Sayı: 1, 48–50. https://ajindex.com/articles/363959

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References (1)

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