Journals / Ege Tıp Dergisi / 1999 / Cilt: 38 - Sayı: 1

"Schwannomatosis": Case report

"Schwannomatosis": Olgu sunumu

Pages
45–47
DOI
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AI Summary & Key Takeaways

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

A case of schwannomatosis was presented in view of the literature

📌 3 Key Takeaways

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Objective & Hypothesis:Schwannomatosis characterized with multiple schwannomas is a rare entity and not associated with clinical signs that are seen in neurofibromatosis.
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Key Findings & Data:Schwannomatosis characterized with multiple schwannomas is a rare entity and not associated with clinical signs that are seen in neurofibromatosis.
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Conclusion & Impact:A case of schwannomatosis was presented in view of the literature
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Nöroendokrin tümörler · Nörofibromatözler · Nörilemoma

Abstract

Schwannomatosis characterized with multiple schwannomas is a rare entity and not associated with clinical signs that are seen in neurofibromatosis. A case of schwannomatosis was presented in view of the literature

Özet

Schwannomatosis, nörofibromatoziste görülen klinik bulguların eşlik etmediği, multipl schwannom varlığı ile karakterli az görülen bir antitedir. Bir schwannomatosis olgusu, kaynaklar eşliğinde sunulmaktadır.

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Cite This Article

VARDAR, E., BÜYÜKKEBABÇI, D., ZENGEL, B., POSTACI, H., DENEÇLİ, A. G., KARAKOYUNLAR, Ö. (1999). "Schwannomatosis": Case report. Ege Tıp Dergisi, Cilt: 38 - Sayı: 1, 45–47. https://ajindex.com/articles/223178