Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ninth thoracic vertebra"'
Publikováno v:
Korean Journal of Spine
We report a case of a 45-year-old man with a complaint of both leg weakness and hypoesthesia. Radiological evaluation revealed an osteolytic lesion of the ninth thoracic vertebra. The patient underwent posterior corpectomy with total excision of the
Publikováno v:
Trauma Monthly
Introduction: Traumatic thoracic spondyloptosis is caused by high energy trauma and is usually associated with severe neurological deficit. Cases presenting without any neurological deficit can be difficult to diagnose and manage. Case Presentation:
Publikováno v:
Emergency Radiology. 13:259-263
In this paper, we report a case of vertebral hemangioma during pregnancy in a 21-year-old woman presenting with paraparesis of rapid onset. An emergency MRI scan of the dorsal spine showed a lesion of the ninth thoracic vertebra with extradural exten
Publikováno v:
Clinical Endocrinology. 46:631-636
Summary A 42-year-old woman had galactorrhoea and amenorrhoea. Four years previously she complained of sensory disturbance of her legs, with gait disturbance. Serum PRL level was 1408 mU/l. Magnetic resonance imaging showed a spindle-shaped mass in t
Publikováno v:
Journal of spinal disorderstechniques. 20(2)
An exceedingly rare complication of Luque segmental spinal instrumentation in spinal fractures is described. A patient was treated for fractures of the eighth and ninth thoracic vertebra associated with traumatic paraplegia using Luque segmental spin
Autor:
Lyle J. Micheli, R W Hood
Publikováno v:
The Journal of Bone & Joint Surgery. 65:992-997
Anterior stabilization of severe structural deformities of the spine, especially kyphoscoliosis, at the cervicothoracic level is a difficult surgical procedure. A new combined procedure including anterolateral cervical and posterior transpleural tran
Autor:
S. N. Basu
Publikováno v:
The Indian Journal of Pediatrics. 25:323-328
A case having multiple sagittal cleft or “butter-fly” vertebrae and hemivertebrae is presented. The record of such coincidence of two rare anomalies in one case could not be found in the literature. Roentgenological investigations of parents and