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1.
Journal of the Korean Shoulder and Elbow Society ; : 261-265, 2015.
Artículo en Inglés | WPRIM | ID: wpr-770721

RESUMEN

Neuropathic shoulder arthropathy or Charcot's shoulder is an extremely rare disease, and sometimes it is associated with cervical syringomyelia. Clinical symptoms of the disease include edema of the shoulder and restriction in range of motion. Radiological diagnosis can be made through plain radiography through a characteristic, atrophic destruction of the joint. We experienced a Charcot's joint of the shoulder wherein destruction of the joint progressed extremely quickly and reviewed the literature concerning this condition.


Asunto(s)
Artropatía Neurógena , Diagnóstico , Edema , Articulaciones , Radiografía , Rango del Movimiento Articular , Enfermedades Raras , Hombro , Siringomielia
2.
Clinics in Shoulder and Elbow ; : 261-265, 2015.
Artículo en Inglés | WPRIM | ID: wpr-197178

RESUMEN

Neuropathic shoulder arthropathy or Charcot's shoulder is an extremely rare disease, and sometimes it is associated with cervical syringomyelia. Clinical symptoms of the disease include edema of the shoulder and restriction in range of motion. Radiological diagnosis can be made through plain radiography through a characteristic, atrophic destruction of the joint. We experienced a Charcot's joint of the shoulder wherein destruction of the joint progressed extremely quickly and reviewed the literature concerning this condition.


Asunto(s)
Artropatía Neurógena , Diagnóstico , Edema , Articulaciones , Radiografía , Rango del Movimiento Articular , Enfermedades Raras , Hombro , Siringomielia
3.
Journal of Korean Neurosurgical Society ; : 718-722, 1995.
Artículo en Coreano | WPRIM | ID: wpr-98445

RESUMEN

The authors present a case of cervical syringomyelia associated with cerebellar mixed oligoastrocytoma in an 18-month-old boy who was normally delivered at full-term. The child presented with an increasing incidence of vomiting and irritability, and a poor truncal control. Preoperative magnetic resonance imaging of the brain revealed cerebellar vermian tumor with an obstructive hydrocephalus and a small-sized syringomyelia at the 6th cervical vertebral level. The tumor was completely removed via suboccipital craniectomy. Histologically, the tumor consisted of mixed oligo-astrocytoma. The cervical syringomyelia was conservatively managed with no specific operative treatment. At two months postoperatively, magnetic resonance imaging of the cervical spine showed a remarkable reduction in size of the syringomyelic cavity.


Asunto(s)
Niño , Humanos , Lactante , Masculino , Astrocitoma , Encéfalo , Neoplasias Cerebelosas , Hidrocefalia , Incidencia , Imagen por Resonancia Magnética , Columna Vertebral , Siringomielia , Vómitos
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