Presentation
Unknown
Patient Data
Age: 25 years
Gender: Female
From the case:
Camurati-Engelmann disease (diaphyseal dysplasia)
{"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/25266/annotated_viewer_json?c=1681077651\u0026lang=us"}
There is diffuse and somewhat irregular thickening of the cortical bone in the diaphyses of all of the long bones, with no involvement of the epiphyses. Interestingly, there are still open physes in this 24 year old, indicating delayed skeletal maturity.
From the case:
Camurati-Engelmann disease (diaphyseal dysplasia)
{"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/27060/annotated_viewer_json?c=1681077651\u0026lang=us"}
Calvarial thickening with a dense diploic space and absence of the frontal and sphenoid sinuses.
Case Discussion
These findings are pathognomonic of diaphyseal dysplasia.
This case is courtesy of the LAC+USC radiology department.
Unable to process the form. Check for errors and try again.