Acquired Chiari I malformation following a lumbo-peritoneal shunt– William’s hypothesis revisited
نویسندگان
چکیده
منابع مشابه
Treatment of Syringomyelia due to Chiari Type I Malformation with Syringo-Subarachnoid-Peritoneal Shunt
Chiari type I malformation is a tonsillar herniation more than 3 mm from the level of foramen magnum, with or without concurrent syringomyelia. Different surgical treatments have been developed for syringomyelia secondary to Chiari's malformations: craniovertebral decompression with or without plugging of the obex, syringo-subarachnoid, syringo-peritoneal, and theco-peritoneal shunt placement. ...
متن کاملAcquired Chiari Malformation: Safety of Neuraxial Anesthesia?
Chiari malformation is a congenital anomaly that primarily involves the downward displacement of the cerebellar tonsils through the foramen magnum and elongation of forth ventricle and lower brainstem. Patients with Chiari I (congenital or acquired) malformation are asymptomatic or may present with neurologic signs and symptoms. It is always a question of safety of neuraxial anesthesia in these...
متن کاملChiari I malformation and delivery
The following recommendations have been adopted and field tested on the patients of our centers for more than 10 years. They reflect the feedback from experts in the field of Obstetrics and Anesthesia, as well as the evolution of our understanding of CMI and syringomyelia. • A trial of natural childbirth is not contraindicated in patients with CMI (untreated, or after surgical decompression) • ...
متن کاملDetection of peritoneal pseudocyst following ventriculo-peritoneal shunt by radionuclide method [Persian]
A 14 years old boy who had a ventriculo-peritoneal shunt since the age of 5 months, was hospitalized due to headaches, nausea, vomiting and abdominal distension. In abdominal CT and sonographic evaluation, pancreatic pseudocyst or mesentric cyst were suspected. Evaluation of the shunt by radionuclide, however, was diagnostic and revealed a pseudocyst at the peritoneal end of the shunt. Th...
متن کاملA genetic hypothesis for Chiari I malformation with or without syringomyelia.
In several reports the authors have suggested occasional familial aggregation of syringomyelia and/or Chiari 1 malformation (CM1). Familial aggregation is one characteristic of traits that have an underlying genetic basis. The authors provide evidence for familial aggregation of CM1 and syringomyelia (CM1/S) in a large series of families, establishing that there may be a genetic component to CM...
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ژورنال
عنوان ژورنال: Journal of Medical and Scientific Research
سال: 2013
ISSN: 2321-1326,2394-112X
DOI: 10.17727/jmsr.2013/1-003