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Journals / ENT Updates / 2017 / Cilt: 7 Sayı: 3

Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report

Özlem Ünsal
Pınar Soytaş
Fevziye Kabukçuoğlu
Berna Uslu Coşkun
Pages
157–160
Publication Date
2017-11-28
DOI
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AI Summary & Key Takeaways

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

In this case report, we presented a young male patient with juvenile psammomatoid ossifying fibroma involving the sinonasal region, skull base and the orbit, which was treated with endoscopic surgery.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Juvenile ossifying fibroma is an uncommon, benign, fibro-osseous neoplasm with aggressive local growth.
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Key Findings & Data:This tumor is distinguished from other fibro-osseous lesions especially by its age of onset, aggressive behavior, and clinical presentation.
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Conclusion & Impact:In this case report, we presented a young male patient with juvenile psammomatoid ossifying fibroma involving the sinonasal region, skull base and the orbit, which was treated with endoscopic surgery.
🔬Design:Araştırma Makalesi
📍Scope:Comprehensive Sample
⚙️Variables:Endoscopic sinus surgery · juvenile ossifying fibroma · psammomatoid variant

Abstract

Juvenile ossifying fibroma is an uncommon, benign, fibro-osseous neoplasm with aggressive local growth. This tumor is distinguished from other fibro-osseous lesions especially by its age of onset, aggressive behavior, and clinical presentation. Two microscopic types have been described: trabecular and psammomatoid variants. In this case report, we presented a young male patient with juvenile psammomatoid ossifying fibroma involving the sinonasal region, skull base and the orbit, which was treated with endoscopic surgery.

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Cite This Article

Ünsal, Ö., Soytaş, P., Kabukçuoğlu, F., Coşkun, B. U. (2017). Juvenile psammomatoid ossifying fibroma with skull base and orbital wall invasion: a rare case report. ENT Updates, Cilt: 7 Sayı: 3, 157–160. https://ajindex.com/articles/1205374

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References (1)

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