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Journals / The European Research Journal / 2023 / Cilt: 9 - Sayı: 1

Paraganglioma admitting with stage-4 hypertensive retinopathy

İsa YILMAZ
Fatma ÖZCAN SIKI
Mehmet ÖZTÜRK
Fuat BUĞRUL
Zeliha Esin ÇELİK
Şükrü ARSLAN
Pages
173–177
Publication Date
2023-01-04
DOI
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AI Summary & Key Takeaways

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

Here, we present a 15-year-old patient diagnosed with the complaint of blurred vision.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Paragangliomas and pheochromocytomas are rare tumors originating in chromaffin cells which are predominantly located in adrenal glands.
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Key Findings & Data:This tumor is generally bilateral and much more rarely seen in pediatric patients.
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Conclusion & Impact:Here, we present a 15-year-old patient diagnosed with the complaint of blurred vision.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Extraadrenal gland neoplasms · paraganglioma · pheochromocytoma

Abstract

Paragangliomas and pheochromocytomas are rare tumors originating in chromaffin cells which are predominantly located in adrenal glands. This tumor is generally bilateral and much more rarely seen in pediatric patients. Sustained or paroxysmal hypertension is the most frequent sign of paragangliomas /pheochromocytoma. Here, we present a 15-year-old patient diagnosed with the complaint of blurred vision.

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Cite This Article

YILMAZ, İ., SIKI, F. Ö., ÖZTÜRK, M., BUĞRUL, F., ÇELİK, Z. E., ARSLAN, Ş. (2023). Paraganglioma admitting with stage-4 hypertensive retinopathy. The European Research Journal, Cilt: 9 - Sayı: 1, 173–177. https://ajindex.com/articles/864997

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