Journal of Clinical Medicine (May 2023)

Overview of Spontaneous Intracranial Hypotension and Differential Diagnosis with Chiari I Malformation

  • Wan Muhammad Nazief Bin Wan Hassan,
  • Francesco Mistretta,
  • Stefano Molinaro,
  • Riccardo Russo,
  • Giovanni Bosco,
  • Andrea Gambino,
  • Mauro Bergui

DOI
https://doi.org/10.3390/jcm12093287
Journal volume & issue
Vol. 12, no. 9
p. 3287

Abstract

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Spontaneous intracranial hypotension (SIH) occurs due to a leakage of the cerebrospinal fluid (CSF) lowering the pressure of subarachnoid space, mostly caused by a dural breach or discogenic microspur. As a result of less support provided by CSF pressure, intracranial structures are stretched downward, leading to a constellation of more or less typical MRI findings, including venous congestion, subdural effusions, brainstem sagging and low-lying cerebellar tonsils. Clinic examination and an MRI are usually enough to allow for the diagnosis; however, finding the location of the dural tear is challenging. SIH shares some MRI features with Chiari malformation type I (CM1), especially low-lying cerebellar tonsils. Since SIH is likely underdiagnosed, these findings could be interpreted as signs of CM1, leading to a misdiagnosis and an incorrect treatment pathway. Medical treatment, including steroids, bed rest, hydration caffeine, and a blind epidural blood patch, have been used in this condition with variable success rates. For some years, CSF venous fistulas have been described as the cause of SIH, and a specific diagnostic and therapeutic pathway have been proposed. The current literature on SIH with a focus on diagnosis, treatment, and differential diagnosis with CM1, is reviewed and discussed.

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