101. Résolution spontanée d’une cavité syringomyélique dans le cadre d’une malformation de Chiari I chez un enfant : à propos d’un cas
- Author
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B. Mallinger, F. Marson, F. Loubes-Lacroix, I. Catalaa, C. Manelfe, and Annick Sevely
- Subjects
congenital, hereditary, and neonatal diseases and abnormalities ,medicine.medical_specialty ,Radiological and Ultrasound Technology ,medicine.diagnostic_test ,business.industry ,Magnetic resonance imaging ,respiratory system ,medicine.disease ,nervous system diseases ,Surgery ,Chiari I malformation ,embryonic structures ,medicine ,Radiology, Nuclear Medicine and imaging ,Syrinx (medicine) ,Headaches ,medicine.symptom ,business ,Nuclear medicine ,Syringomyelia - Abstract
Cervicothoracic syringomyelia is a frequent feature in Chiari I malformation. It can be symptomatic or not, and is well demonstrated by magnetic resonance imaging (MRI). Its spontaneous resolution is uncommon. The authors report a case of spontaneous resolution of a thoracic syrinx in an 18-year-old patient with a Chiari I malformation. MRI study performed 6 years previously because of worsening headaches demonstrated a Chiari I malformation associated with a syrinx cavity. The cavity disappearance was noted after improvement of the symptoms.
- Published
- 2004
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