Hosting 721 files, 2924 images, and 4 contributors.

Random Case

Sinonasal Ewing Sarcoma
Joseph Junewick, MD FACR
over 8 years ago
Enter A Workflow
Standard2   Academic2

Please choose a workflow. A standard workflow allows you to browse the repository with full case detail; the academic workflow allows you to browse the repository with limited case detail revealed. Double click on the images to launch image viewer.

ARSt Case Repository

Case History

6 year old male with intermittent hip pain for several months, acutely worsened after climbing the sand dunes.

Case Detail

Anatomy: Musculoskeletal
Joseph Junewick, MD FACR
Diagnostic Category: Trauma
Created: over 7 years ago
Updated: over 7 years ago
Tags: PEDS
Modality/Study Types: CR CT
Adobe32 PDF Imagej32 ImageJA

Case Images

Academic Case Revealer (Click to Expand)

Reveal Findings

CR – Neutral and abduction views show coxa valga and slipped left capital femoral epiphysis. Also note that the height of the femoral epiphyses is decreased.

CT – Axial and sagittal images show the femoral head to be posterior relative to the neck. Note the buttressing posteriorly at the neck near the physis related to attempted healing, indicating an acute on chronic process.

Reveal Discussion

Slipped capital femoral epiphysis (SCFE) is a relatively atraumatic fracture through the proximal femoral physis. SCFE is the most common hip malady in adolescents, affecting males more than females and African-Americans more than caucasions. SCFE prior to adolescence suggests underlying process such as malnutrition, endocrinopathy, developmental dysplasia, and coxa valga. Pathophysiology is probably related to oblique orientation of the physis and increased body weight and activity (particularly abduction, external rotation and extension) during adolescence.

Valgus displacement often presents with a relatively normal appearance on anteroposterior radiographs. Valgus SCFE may be associated with obesity, coxa valga, hypopituitarism, and Stickler syndrome. Posterolateral displacement of the femoral epiphysis makes in situ fixation of valgus SCFE more difficult, due to the necessity of a more medial starting point.

Stickler syndrome is connective tissue disease characterized by midface hypoplasia, cleft palate, myopia, sensorineural hearing loss, joint hypermobility, and epiphyseal dysplasia (short stature). Radiographically there is mild to moderateflattening of the vertebral bodies, undermodeling of the long bones with broad epiphyses (particularly the femora and tibiae), and premature arthropathy. Stickler syndrome is an autosomal dominant with marked intrafamilial and mutation-dependent variability; the molecular defect is related to the COL2A1 gene.

Reveal Diagnosis

Posterior Slipped Capital Femoral Epiphysis – Probable Stickler Syndrome

Corporate Office: 616.363.7272, 3264 North Evergreen Drive, Grand Rapids, MI 49525

Spectrum Health Helen Devos Childrens Hospital GE HealthCare