Scopus
YÖKSİS Eşleşti
An Extremely Rare Case of Ollier Disease With Calvarial Involvement
Clinical Nuclear Medicine · Ocak 2025
YÖKSİS Kayıtları
An Extremely Rare Case of Ollier Disease With Calvarial Involvement
Clinical Nuclear Medicine · 2025 SCI-Expanded
DOÇENT HASAN ÖNNER →
Makale Bilgileri
DergiClinical Nuclear Medicine
Yayın TarihiOcak 2025
Scopus ID2-s2.0-105014273174
Özet
First described by Ollier in 1899, Ollier disease is a rare, nonhereditary skeletal condition characterized by multiple enchondromas. Enchondromatosis can present bilaterally, often with a predominant side, and may manifest as monomelic or hemiskeletal involvement. Significant clinical challenges in Ollier disease include progressive limb shortening, angular deformities, and an elevated risk of pathologic fractures. In adult patients, malignant transformation is a potential concern. Calvarial involvement in Ollier disease is exceedingly rare, with only a few documented cases. Most reported instances of calvarial involvement pertain to the skull base rather than the calvarial bones. Herein, we present a case of Ollier disease with multifocal enchondromas, including involvement of the calvarium, identified through whole-body bone scintigraphy.
Yazarlar (3)
1
H. Önner
ORCID: 0000-0003-1002-2097
2
M. N. Calderon Tobar
3
L. Perktaş
Anahtar Kelimeler
bone scintigraphy
calvarial involvement
Ollier disease
Kurumlar
Selçuk Tip Fakültesi
Konya Turkey