We report a series of four cases of congenital high scapula (or Sprengel's deformity) diagnosed and followed in our establishment. The main feature of this very rare congenital malformation of the pectoral girdle is an abnormally high, more or less dysmorphic scapula. A congenitally high scapula is often discovered in young children, when consequences for aesthetics, and sometimes functional difficulties, are brought to light. When surgical treatment is envisaged, imaging is recommended to diagnose a supernumerary structure, ossified (an omovertebral bone) or not (a fibrous and/or cartilaginous connection), extending from the scapula to the cervical spine. This needs to be resected. A CT scan is essential for detecting an omovertebral bone and the vertebral bone abnormalities that are often associated with it. MRI and ultrasound are very useful for assessing any fibrous and/or cartilaginous components. An ultrasound examination has the undeniable advantage of being quick and easy in these young children.
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http://dx.doi.org/10.1016/j.diii.2012.08.006 | DOI Listing |
Neurol India
November 2024
Department of Radiodiagnosis, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
Radiol Case Rep
January 2025
Department of Emergency Radiology. Ibn Sina University Hospital, Mohammed V University, Rabat, Morocco.
The features of Sprengel's deformity, also known as congenital high scapula, include abnormal positioning and dysplasia of the affected scapula, with a possible omovertebral connection or atrophy of the surrounding muscles. This case primarily aims to present the CT scan findings of a 19-year-old male with Sprengel deformity. Imaging enables the definitive diagnosis of this congenital malformation, and allows for the detection of associated anomalies, particularly the presence of the omovertebral bone, thereby facilitating appropriate management.
View Article and Find Full Text PDFKlippel-Feil syndrome (KFS) is a rare congenital disorder characterized by the fusion of cervical vertebrae, limiting neck mobility, and often presenting with clinical manifestations such as neck pain, stiffness, and neurological deficits. While the classical presentation of KFS includes a "clinical triad" comprising a shortened neck, a low posterior hairline, and limited cervical motion, not all patients exhibit all three features. This case report presents an 81-year-old male with the complete KFS triad and underscores the diagnostic challenges and management strategies associated with this condition.
View Article and Find Full Text PDFPediatr Neonatol
September 2024
Diagnostic and Interventional Radiology, IRCCS Istituto Ortopedico Rizzoli, 40136, Bologna, Italy. Electronic address:
Neurol India
March 2024
Department of Neuro Physiotherapy, Ravi Nair Physiotherapy College, Datta Meghe Institute of Higher Education and Research, Sawangi, Wardha, Maharashtra, India.
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