RESUMO
Sprengel deformity is a congenital abnormality done to the ascent of the scapular bone (which occurs probably between the 5th and 12th weeks of gestation). It can cause cosmetic or functional problems. The aim of our study was to describe this rare deformity, often neglected in our context, and its surgical management. We report a case of a 16-year-old boy with a Sprengel deformity associated with omovertebral intracanalar compressive bone seen on the CT scan. He reported neurological symptoms such as spastic paraparesis and walk disturbances. The bone was resected surgically and physiotherapy was set up. The outcome was good with noticeable neurological improvement of walk and balance, recovery of autonomy. Sprengel deformity is a rare pathology. Surgery must be done early and be adapted to the case.
Assuntos
Neurocirurgia , Articulação do Ombro , Adolescente , Países em Desenvolvimento , Humanos , Masculino , Escápula , Tomografia Computadorizada por Raios XRESUMO
Epidural lipomatosis is characterized by the abnormal accumulation of non-encapsulated grease in the epidural space. Although rare, it is a possible cause of lombosciatica or narrow lumbar channel. It is often associated with contributing factors such as prolonged corticosteroid therapy or obesity. We report the case of a patient presenting with disabling lombosciatalgias. Radiological evaluation confirmed the diagnosis of compressive epidural lipomatosis. Patient's evolution was favorable after surgical decompression.