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Journals / Acta Oncologica Turcica / 2026 / Cilt: 47 Sayı: 1

Isolated Sessile Chondrosarcoma Arising in Osteochondroma: A Case Report

İzole Sesil Osteokondrom Zemininde Gelişen Kondrosarkom: Olgu Sunumu

Mahmut Kalem
Reşit Sevimli
Adem Ünlü
Yener Sağlık
Pages
16–18
Publication Date
2014-08-21
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AI Summary & Key Takeaways

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

Causing severe pain and surgical treatment is recommended due to the risk of development chondrosarcoma.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Osteochondroma of the most common benign bone tumors are from youth, mostly in the metaphyses of long bones is determined as a single mass.
📊
Key Findings & Data:Causing severe pain and surgical treatment is recommended due to the risk of development chondrosarcoma.
💡
Conclusion & Impact:In this paper, an osteochondroma arising from the proximal humerus osteochondroma developed in the case of chondrosarcoma diagnosis, treatment and follow-up of patients was presented.
🔬Design:Makale
📍Scope:Comprehensive Sample
⚙️Variables:Humerus · kondrosarkom · osteokondrom

Abstract

Osteochondroma of the most common benign bone tumors are from youth, mostly in the metaphyses of long bones is determined as a single mass. Causing severe pain and surgical treatment is recommended due to the risk of development chondrosarcoma. In this paper, an osteochondroma arising from the proximal humerus osteochondroma developed in the case of chondrosarcoma diagnosis, treatment and follow-up of patients was presented.

Özet

Osteokondrom benign kemik tümörlerinin en sık görülenlerindendir, Çoğunlukla uzun kemiklerin metafizinde tek bir kitle olarak saptanır. Sıklıkla ağrıya sebep olması ve kondrosarkom gelişme riskindan dolayı cerrahi tedavi onerilmektedir. Bu yazıda, proksimal humerustan kaynaklanan bir osteokondrom zemininde gelişen sekonder kondrosarkom olgusunun tanı-tedavi ve takip sonucu sunuldu.

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Cite This Article

Kalem, M., Sevimli, R., Ünlü, A., Sağlık, Y. (2014). Isolated Sessile Chondrosarcoma Arising in Osteochondroma: A Case Report. Acta Oncologica Turcica, Cilt: 47 Sayı: 1, 16–18. https://doi.org/10.5505/aot.2014.87597

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