4.5 Article

Popping the balloon: Abrupt onset of a spinal CSF leak and spontaneous intracranial hypotension in idiopathic intracranial hypertension, a case report

Journal

HEADACHE
Volume 62, Issue 2, Pages 208-211

Publisher

WILEY
DOI: 10.1111/head.14264

Keywords

cerebrospinal fluid leak; idiopathic intracranial hypertension; intracranial hypertension; intracranial hypotension; neuroimaging; spontaneous intracranial hypotension

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This study reports a case of a patient with idiopathic intracranial hypertension who developed a spinal cerebrospinal fluid leak and subsequent spontaneous intracranial hypotension following a pressure-elevating maneuver. The findings raise questions about a potential causative link between elevated CSF pressure and the development of spontaneous intracranial hypotension, and suggest the potential prophylactic benefit of lowering CSF pressure in preventing this condition.
Objectives Spontaneous intracranial hypotension (SIH) is a debilitating neurologic condition that is often thought of as separate from idiopathic intracranial hypertension (IIH). The unique case presented here details a spontaneous spinal cerebrospinal fluid (CSF) leak that developed abruptly following a CSF pressure elevating maneuver in a patient with pre-existing intracranial hypertension, raising the possibility of a causative link between the two conditions. Results A 40-year-old woman with symptomatic IIH developed a dural tear of a thoracic spinal nerve root sleeve during an episode of Valsalva maneuver leading to a CSF leak and development of symptomatic SIH. This was successfully treated with epidural blood and fibrin glue patch and the patient is now symptom-free. Discussion The implication of a possible causative link between elevated CSF pressure and subsequent development of dural rupture and SIH raises important questions regarding the pathophysiology of SIH in some cases. Furthermore, it suggests that there could be a potential prophylactic benefit of CSF pressure lowering medications in preventing the development of SIH in patients with IIH.

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