Literature DB >> 21156430

Spontaneous intracranial hypotension: case series of rare clinical presentations.

N Chaudhary1, P Cooper, S P Lownie, W Ng, N Duggal.   

Abstract

BACKGROUND: Spontaneous intracranial hypotension (SIH) is an increasingly described entity, with over 70 cases reported in the literature. The classic triad includes orthostatic headache, diffuse pachymeningeal enhancement on magnetic resonance imaging (MRI) with gadolinium, and low cerebrospinal fluid pressure (CSF) in the lateral decubitus (< 60 mm H₂O) and sitting positions.
METHOD: We present four rare clinical presentations of SIH, two of which have not been previously described in the literature, to the best of our knowledge.
RESULTS: Patient 1 presented with dyspnea, dysphagia, bilateral ptosis, diplopia and seizures. Patient 2 presented with a paradoxical positional pattern of orthostatic hypotension. In Patient 3, bilateral subdural hematomas (SDH) were encountered; while in Patient 4, a recurrent unilateral SDH requiring multiple surgical interventions was demonstrated.
CONCLUSION: Although uncommon clinical presentations, all four cases of intracranial hypotension were spontaneous, demonstrated diagnostic MRI findings, and responded favorably to blood patches or saline injections.

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Mesh:

Year:  2011        PMID: 21156430     DOI: 10.1017/s0317167100011070

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  2 in total

1.  Concentric visual field defect related to spontaneous intracranial hypotension.

Authors:  Belen Pilo-de-la-Fuente; Julio Gonzalez Martin-Moro; Francisco Navacerrada; Francisco Jose Plaza-Nieto; Felix Javier Jimenez-Jimenez
Journal:  Int Ophthalmol       Date:  2013-01-01       Impact factor: 2.031

2.  Seizures and Consciousness Disorder Secondary to Intracranial Hypotension After Spinal Surgery: A Case Report and Literature Review.

Authors:  Yuqing Lv; Hui Xiang
Journal:  Front Neurol       Date:  2022-06-27       Impact factor: 4.086

  2 in total

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