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The rare sprengel deformity: our experience with three cases
Antonia Bindoudi1, Eleni P Kariki1, Konstantinos Vasiliadis1
1Department of Radiology, Papageorgiou General Hospital, Thessaloniki, Greece.
Sprengel shoulder, a rare congenital scapula defect, is typically diagnosed at birth. Advanced imaging like CT and MRI aid in assessing associated abnormalities and planning treatment for this common congenital scapular anomaly.
Area of Science:
- Orthopedics
- Pediatric Radiology
- Medical Imaging
Background:
- Sprengel shoulder is a rare congenital deformity affecting one or both scapulae, characterized by the failure of the scapula to descend during fetal development.
- While often sporadic, familial cases of Sprengel shoulder have been documented, and it is frequently associated with Klippel-Feil syndrome and other skeletal anomalies.
Observation:
- This case series presents imaging experiences from three pediatric patients diagnosed with Sprengel shoulder.
- The study highlights the diagnostic utility of conventional radiography and advanced imaging modalities such as computed tomography (CT) and magnetic resonance (MR) scans.
Findings:
- Anteroposterior X-ray imaging is effective for diagnosing Sprengel deformity.
- CT and MR scans with 3D reconstruction are crucial for identifying concomitant abnormalities, detailed anatomical assessment, and surgical planning.
Implications:
- Understanding the imaging characteristics of Sprengel shoulder is vital for accurate diagnosis and management in pediatric cases.
- This discussion aims to enhance awareness and inform clinical practice regarding this common congenital scapular defect.
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