Presentation
Limb deformity.
Patient Data
Age: 6 years
Gender: Male
From the case:
Ollier disease
{"current_user":null,"step_through_annotations":true,"access":{"can_edit":false,"can_download":true,"can_toggle_annotations":true,"can_feature":false,"can_examine_pipeline_reports":false,"can_pin":false},"extraPropsURL":"/studies/100592/annotated_viewer_json?lang=us"}
There are multiple pelvic and bilateral lower limb bony expansile lesions with broadened shaft at the end of long bones and patchy calcifications.
Case Discussion
Enchondromatosis, also known as Ollier disease, is a non-hereditary, sporadic, skeletal disorder characterized by multiple enchondromas principally located in the metaphyseal regions.
Unable to process the form. Check for errors and try again.