Spontaneous Intracranial Hypotension: Headache With a Reversible Arnold-Chiari Malformation

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منابع مشابه

Delirium, headache, and the type I Arnold-Chiari malformation.

Acute delirium can occur in a variety of states including migraine, l head trauma,2 nonconvulsive status epilepticus,3 and cerebral infarction.4 Acute delirium accompanied by migrainous headache is much more common in children than adults and is termed acute confusional migraine.s In 1883 John Cleland, a British poet and anatomist, first described the abnormality of the brainstem and cerebellum...

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[Arnold-Chiari malformation].

Address for Correspondence: Dr. Joseph Abraham, Department of Anatomy, Government Medical College and Hospital, Chandigarh 32, India, 160030. Phone No.: +919041466127. E-Mail: [email protected] Chiari malformations (CM) are named for Hans Chiari, an Austrian pathologist, who first identified type I-III in 1891. This study was conducted on 400 fetuses obtained from department of Obstetrics an...

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Spontaneous Intracranial Hypotension Presenting as a "Pseudo-Chiari 1

Spontaneous intracranial hypotension (SIH) is classified as a decrease in cerebrospinal fluid (CSF) pressure secondary to a CSF leakage and consequent descent of the brain into the foramen magnum. Diagnosing SIH can be difficult due to its overlapping findings with Arnold-Chiari type 1 Malformation (CM1) where the cerebellar tonsils herniate into the foramen magnum. The similarity of both condi...

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Acute Porphyria in a Patient with Arnold Chiari Malformation

BACKGROUND Acute porphyria and Arnold Chiari malformation are both uncommon genetic disorders without known association. The insidious onset, non-specific clinical manifestations, and precipitating factors often cause diagnosis of acute porphyria to be missed, particularly in patients with comorbidities. CASE REPORT A women with Arnold Chiari malformation type II who was treated with oxybutyn...

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Arnold-Chiari Malformation Type III With Meningoencephalocele: A Case Report

Arnold-Chiari malformation type III (CM III) is an extremely rare anomaly with poor prognosis. An encephalocele with brain anomalies as seen in CM II, and herniation of posterior fossa contents like the cerebellum are found in CM III. The female infant was a twin, born at 33 weeks, weighing 1.7 kg with a huge hydrocele on the craniocervical junction. After operations were performed, she was ref...

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ژورنال

عنوان ژورنال: Headache: The Journal of Head and Face Pain

سال: 1995

ISSN: 0017-8748,1526-4610

DOI: 10.1111/j.1526-4610.1995.hed3509557.x