Web01. jun 2015. · Ollier disease (Spranger type I) is a rare bone disease that is characterized by multiple enchondromatosis with a typical asymmetrical distribution and confined to the appendicular skeleton. ... In this article, various radiological features of Ollier disease, including radiographs, computed tomography, and magnetic resonance imaging, are also ... Web23. jul 2016. · Purpose . The purpose of our study was to investigate clinical manifestations, roentgen images, histopathological studies, and evolution of the disease in patient displaying infantile cortical hyperostosis. Methods . Roentgenograms were made to evaluate a neonatal patient presenting multiple soft-tissue swellings. The initial radiographs …
Diffuse midline glioma in Ollier disease: A case report and a brief ...
Web28. maj 2009. · Introduction Ollier's disease is a rare nonhereditary disorder characterized by multiple enchondromas with a predilection for unilateral distribution. Malignant … Web12. avg 2024. · Ollier disease is usually diagnosed during childhood. Symptoms are not typically apparent at birth, though skeletal abnormalities may sometimes be noted early … bologna university in germany
Bilateral multiple malignant transformation of Ollier’s disease
Web02. dec 2024. · Ollier’s disease is a non-hereditary, benign bone tumor which is usually characterized by presence of multiple radiolucent lesions (enchondromas) in the … WebMaffucci syndrome is a disorder that primarily affects the bones and skin. It is characterized by multiple enchondromas, which are noncancerous (benign) growths of cartilage that … WebThe purpose of this paper is to correlate the roentgenologic, pathologic, and clinical findings in polyostotic fibrous dysplasia, as indicated in a report of four cases; to present the … bologna university phd call 2023