AbstractCervical dysraphism is rare, and the 3 recognized subtypes manifest as cystic, skin-covered masses. To our knowledge, no case of cervical lipomyelocele has been reported in the literature so far. We present a case of surgically and pathologically confirmed cervical lipomyelocele in a patient with spondylocostal dysostosis and multiple other congenital anomalies and a brief review of the literature. In this case, magnetic resonance imaging demonstrates fat extension into a dysraphic cervical spinal canal, allowing for preoperative diagnosis. Computed tomography using 3-dimensional reconstruction serves to more clearly characterize the extensive spine malsegmentation characteristic of spondylocostal dysostosis. The use of this techniq...
A rare high cervical intradural subpial lipoma unassociated with spinal dysraphism manifested by a s...
Background: Cystic dysraphic lesions of the cervical and upper thoracic region are rare and only a f...
Seven cases of adult spinal vascular malformations presenting in conjunction with spinal dysraphism ...
Cervical dysraphism is rare, and the 3 recognized subtypes manifest as cystic, skin-covered masses. ...
AbstractCervical dysraphism is rare, and the 3 recognized subtypes manifest as cystic, skin-covered ...
Lateral sacral lipomyelomeningocele is a rare spinal developmental anomaly. In the case under report...
Cervical lipomyelomeningocele is a very rare form of spina bifida occulta, which can cause some comp...
A patient with lipomyelomeningocele (known in utero) presented for MRI characterization prior to sur...
AbstractA patient with lipomyelomeningocele (known in utero) presented for MRI characterization prio...
International audienceBackground: Congenital spinal lipomas are closed spinal dysraphisms belonging ...
The results of a retrospective study of 10 cases of lipomyelomeningocele (LMML) and 4 cases of spina...
Two cases of lipoma of the spinal cord are presented. CT gives a specific diagnosis in this conditio...
Background: Intradural spinal lipomas without an associated dysraphism, represent a fraction of an a...
We report the MRI dorsolumbar spine of 10-year child who was referred to the Civil Hospital in June ...
Myelocystocele is a rare variety of spinal dysraphism that presents as a skin covered, midline, lumb...
A rare high cervical intradural subpial lipoma unassociated with spinal dysraphism manifested by a s...
Background: Cystic dysraphic lesions of the cervical and upper thoracic region are rare and only a f...
Seven cases of adult spinal vascular malformations presenting in conjunction with spinal dysraphism ...
Cervical dysraphism is rare, and the 3 recognized subtypes manifest as cystic, skin-covered masses. ...
AbstractCervical dysraphism is rare, and the 3 recognized subtypes manifest as cystic, skin-covered ...
Lateral sacral lipomyelomeningocele is a rare spinal developmental anomaly. In the case under report...
Cervical lipomyelomeningocele is a very rare form of spina bifida occulta, which can cause some comp...
A patient with lipomyelomeningocele (known in utero) presented for MRI characterization prior to sur...
AbstractA patient with lipomyelomeningocele (known in utero) presented for MRI characterization prio...
International audienceBackground: Congenital spinal lipomas are closed spinal dysraphisms belonging ...
The results of a retrospective study of 10 cases of lipomyelomeningocele (LMML) and 4 cases of spina...
Two cases of lipoma of the spinal cord are presented. CT gives a specific diagnosis in this conditio...
Background: Intradural spinal lipomas without an associated dysraphism, represent a fraction of an a...
We report the MRI dorsolumbar spine of 10-year child who was referred to the Civil Hospital in June ...
Myelocystocele is a rare variety of spinal dysraphism that presents as a skin covered, midline, lumb...
A rare high cervical intradural subpial lipoma unassociated with spinal dysraphism manifested by a s...
Background: Cystic dysraphic lesions of the cervical and upper thoracic region are rare and only a f...
Seven cases of adult spinal vascular malformations presenting in conjunction with spinal dysraphism ...