Spontaneous intracranial hypotension: two steroid-responsive cases
نویسندگان
چکیده
منابع مشابه
Two Cases of Secondary Intracranial Hypotension
The unique symptom of intracranial hypotension (IH) is an orthostatic headache caused by low cerebrospinal fluid (CSF) pressure and is not so rare. IH results from loss of CSF caused by a dural defect in the spine, cranial vault, or skull base. The classic orthostatic headache commences within 15 minutes, but occasionally symptoms last up to several hours, after standing or upright sitting posi...
متن کاملSpontaneous intracranial hypotension.
From the Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan; Department of Anatomy and Cell Biology, National Taiwan University College of Medicine, Taipei, Taiwan. Received January 10, 2005. Revised and Accepted January 21, 2005. Reprint requests and correspondence to: Sung-Tsang Hsieh. MD. Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan. ...
متن کاملSpontaneous intracranial hypotension.
Spontaneous intracranial hypotension (SIH) is an increasingly recognised syndrome. Postural headache with typical findings on magnetic resonance imaging (MRI) are the key to diagnosis. Orthostatic headache, low cerebrospinal fluid opening pressure, and diffuse meningeal enhancement on post-contrast T1-weighted MRI brain studies are the major features of this increasingly recognised syndrome. He...
متن کاملSpontaneous intracranial hypotension.
Spontaneous intracranial hypotension is a rare benign and usually self-limited condition of unknown aetiology. Four cases are presented that illustrate how the MRI features may support a diagnosis suggested on clinical grounds. The MRI findings include diffuse symmetric smooth dural thickening and enhancement, not only at the cranial level, but also involving the cervical spinal dura, subdural ...
متن کاملSpontaneous intracranial hypotension with camptocormia.
Camptocormia is defined as an abnormal flexion of the thoracolumbar spine that appears while standing or walking. It is associated with several clinical situations such as parkinsonism, dystonia, and neuromuscular disorders. We present the case of a 33-year-old man who had marked camptocormia with acute onset (video on the Neurology® Web site at Neurology.org). The patient also had a 2-day hist...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Polish Journal of Radiology
سال: 2018
ISSN: 1899-0967
DOI: 10.5114/pjr.2018.76380