Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Book Review
Brief Report
Case Letter
Case Report
Case Series
Commentary
Current Issue
Editorial
Erratum
Guest Editorial
Images
Images in Neurology
Images in Neuroscience
Images in Neurosciences
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Media and News
None
Notice of Retraction
Obituary
Original Article
Point of View
Position Paper
Review Article
Short Communication
Systematic Review
Systematic Review Article
Technical Note
Techniques in Neurosurgery
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Book Review
Brief Report
Case Letter
Case Report
Case Series
Commentary
Current Issue
Editorial
Erratum
Guest Editorial
Images
Images in Neurology
Images in Neuroscience
Images in Neurosciences
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Media and News
None
Notice of Retraction
Obituary
Original Article
Point of View
Position Paper
Review Article
Short Communication
Systematic Review
Systematic Review Article
Technical Note
Techniques in Neurosurgery
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Search in posts
Search in pages
Filter by Categories
Book Review
Brief Report
Case Letter
Case Report
Case Series
Commentary
Current Issue
Editorial
Erratum
Guest Editorial
Images
Images in Neurology
Images in Neuroscience
Images in Neurosciences
Letter to Editor
Letter to the Editor
Letters to Editor
Letters to the Editor
Media and News
None
Notice of Retraction
Obituary
Original Article
Point of View
Position Paper
Review Article
Short Communication
Systematic Review
Systematic Review Article
Technical Note
Techniques in Neurosurgery
View/Download PDF

Translate this page into:

Brief Report
11 (
1
); 170-174
doi:
10.1055/s-0039-3402621

Is Magnetic Resonance Imaging Diffusion Restriction of the Optic Disc Head a New Marker for Idiopathic Intracranial Hypertension?

Department of Neurology, Columbia University, New York, New York, United States
Department of Neurology, University of Missouri, Columbia, Missouri, United States

Elanagan Nagarajan, MD Department of Neurology, Columbia University New York, 710 West 168th Street, NY 10032 United States en2452@cumc.columbia.edu

Licence
This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Disclaimer:
This article was originally published by Thieme Medical and Scientific Publishers Private Ltd. and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Abstract

Background Idiopathic intracranial hypertension (IIH) is a headache syndrome due to raised intracranial pressure of unknown etiology. Before making the diagnosis of IIH, secondary causes of raised intracranial pressure must be ruled out. The radiological features associated with this condition have variable sensitivity and specificity. In this case series, we aim to describe a potential new radiological marker of IIH, that is, diffusion restriction, in the optic disc head and propose that this can be a specific finding in the appropriate clinical picture.

Importance IIH causes vision loss and disabling daily headaches. The diagnosis of this condition is based on history and physical examination findings. Magnetic resonance imaging (MRI) is used to exclude other causes, but specific radiological markers for the diagnosis of IIH are lacking.

Observations Five patients presented with the main complaint of headache, which was associated with blurry vision. All of our patients had a formal neuro-ophthalmological evaluation that confirmed the presence of optic disc edema in both eyes. They also underwent an MRI of the brain that showed diffusion restriction in the optic nerve head in either eye or both eyes. Patients underwent lumbar puncture in the lateral decubitus position, which revealed cerebrospinal fluid opening pressures > 25 cm H2O. They all responded well to standard treatments, with the resolution of symptoms in their follow-up appointments.

Conclusion and Relevance The MRI diffusion restriction in the optic nerve head may be a reliable noninvasive marker for the diagnosis of IIH in the appropriate clinical picture.

Keywords

idiopathic intracranial hypertension
pseudotumor cerebri
papilledema
diffusion restriction

Introduction

Headaches are one of the leading causes of both outpatient and emergency room visits and are an important public health problem, particularly among women during their reproductive years. Migraine is the most common headache disorder in this age group followed by idiopathic intracranial hypertension (IIH).1 IIH is a well-characterized headache syndrome caused by elevated intracranial pressure (ICP) of unknown etiology. It causes significant morbidity in untreated cases, including permanent vision loss, and therefore early diagnosis and intervention is warranted.2 Magnetic resonance imaging (MRI) is the imaging modality of choice to rule out other potential causes of raised ICP. Common neuroimaging findings in patients with IIH include empty sella, flattening of the posterior globes, distention of the optic nerve sheaths (ONSs), cerebellar tonsillar herniation, meningoceles, and transverse venous sinus stenosis.3 All these reported MRI findings have high sensitivity and specificity in diagnosing patients with IIH.3 4 5

In this case series, we present five patients with IIH who had diffusion restriction in one or both optic discs with a corresponding apparent diffusion coefficient (ADC) correlate.

Methods

The study was reviewed and approved by the Institutional Review Board of the University of Missouri Hospital.

Case 1

A 29-year-old Hispanic female presented to our emergency department with a 5-day history of headache. The headache was associated with blurry vision, nausea, and vomiting. She was on tacrolimus because of focal segmental glomerular sclerosis. She was evaluated by a neuro-ophthalmologist and noted to have grade 2 optic disc edema in the left eye and grade 5 optic disc edema in the right eye along with subtle hemorrhage. The MRI of her brain showed edema and restricted diffusion in the optic papillae bilaterally, suggestive of ischemic changes (Fig. 1). There were no other abnormal findings on MRI of the brain. Magnetic resonance (MR) venogram did not show any major vessel occlusion or stenosis. Lumbar puncture showed an opening pressure of 50 cm H2O. These findings in the context of her clinical presentation and examination were consistent with IIH. She was started on acetazolamide, and tacrolimus was stopped. Her headache improved significantly by the time of discharge.

Fig. 1 MRI (magnetic resonance imaging) of the brain showing edema and restricted diffusion in the optic papillae bilaterally, suggestive of ischemic changes.

Fig. 1 MRI (magnetic resonance imaging) of the brain showing edema and restricted diffusion in the optic papillae bilaterally, suggestive of ischemic changes.

Case 2

A 20-year-old Caucasian female with no significant past medical history, except for recent steady weight gain, presented to our ophthalmology clinic for an evaluation of occasional headaches. These headaches were associated with pulsating tinnitus and occasional pressure in the back of her eye. The headaches were not associated with photophobia, nausea, emesis or, alteration by positional changes. Funduscopic examination showed grade 2 optic disc edema in the right eye and grade 3 optic disc edema in the left eye. Humphrey’s visual field (HVF) testing showed enlargement of blind spots in both eyes and nasal scotoma in the left eye. The MRI of the brain showed edema and restricted diffusion in the optic papillae bilaterally, more pronounced in the right eye (Fig. 2). The papillae also demonstrated mild postcontrast enhancement. MR venogram showed a hypoplastic left transverse sinus, but no significant vessel stenosis or occlusion was noted. Lumbar puncture showed an elevated opening pressure of 35 cm H20. The patient was started on acetazolamide. Her subsequent clinic visit showed improvement in papilledema (grade 1 in the right eye and grade 2 in the left eye). HVF testing also showed improvement of blind spots in both eyes and nasal scotoma in the left eye that has improved from the previous clinic visit.

Fig. 2 MRI (magnetic resonance imaging) of the brain showing edema and restricted diffusion in the optic papillae bilaterally, which is more pronounced in the right eye.

Fig. 2 MRI (magnetic resonance imaging) of the brain showing edema and restricted diffusion in the optic papillae bilaterally, which is more pronounced in the right eye.

Case 3

A 26-year-old Caucasian female presented to our emergency department with a 5-day history of intermittent binocular diplopia and headache. She complained of retro-orbital pain that was more pronounced in the left eye with occasional floaters. She was noted to have a weight gain of 10 pounds over the past 6 months. Funduscopic examination revealed bilateral optic disc edema (grade 2 in the left eye and grade 1 in the right eye) along with mild left lateral rectus palsy. The MRI of her brain showed edema, restricted diffusion, and postcontrast enhancement in the optic papillae bilaterally that was more pronounced on the left side (Fig. 3A). MR venogram did not show any major vessel occlusion or stenosis. Lumbar puncture showed an elevated opening pressure of 37 cm H20. HVF showed peripheral scotoma on the right and dense central scotoma on the left. The diagnosis of IIH was made and the patient was started on acetazolamide. The intensity and frequency of headaches improved at her subsequent clinical visit. But the patient was not able to tolerate the acetazolamide due to nausea, and subsequently a lumboperitoneal shunt was placed. The repeat MRI after the shunt placement did not show any evidence of edema of the optic disc (Fig. 3B).

Fig. 3 (A) MRI (magnetic resonance imaging) of the brain showing edema, restricted diffusion, and postcontrast enhancement in the optic papillae bilaterally that was more pronounced in the left eye. (B) The repeat MRI (magnetic resonance imaging) after the shunt placement did not show any evidence of edema of the optic disc.

Fig. 3 (A) MRI (magnetic resonance imaging) of the brain showing edema, restricted diffusion, and postcontrast enhancement in the optic papillae bilaterally that was more pronounced in the left eye. (B) The repeat MRI (magnetic resonance imaging) after the shunt placement did not show any evidence of edema of the optic disc.

Case 4

A 26-year-old Caucasian male presented to the hospital with a 3-week history of blurry vision in both eyes. His vision was worse in the right eye and was associated with dark spots and a mild headache. He reported a weight gain of 20 pounds in the past 6 months. Funduscopic examination revealed grade 4 optic disc edema in the right eye and grade 3 in the left eye with peripapillary hemorrhage. MRI of his brain with contrast showed edema and restricted diffusion in the optic papillae bilaterally, significantly more so in the right eye than the left eye (Fig. 4). Venous sinuses did not show any abnormality. Lumbar puncture revealed an opening pressure of 55 cm H20. He was started on acetazolamide. During the follow-up, the patient had worsening of headache and blurry vision and therefore underwent optic nerve sheath (ONS) fenestration.

Fig. 4 MRI (magnetic resonance imaging) of the brain with contrast showing edema and restricted diffusion in the optic papillae bilaterally, significantly more so in the right eye than the left eye.

Fig. 4 MRI (magnetic resonance imaging) of the brain with contrast showing edema and restricted diffusion in the optic papillae bilaterally, significantly more so in the right eye than the left eye.

Case 5

A 23-year-old right-handed woman presented with a 4-day history of blurry vision. She describes her visual disturbance as a painful blurring in both eyes (greater in the right eye) and double vision along with seeing flashes of light and floaters. She also had vertical gaze paresis. The patient was evaluated by a neuro-ophthalmologist and was found to have a grade 4 papilledema bilaterally. HVF showed constriction of peripheral visual field in both eyes (greater in the right eye). MRI of the brain with contrast showed edema and diffusion restriction in the bilateral optic papillae, more significantly in the right eye (Fig. 5). Lumbar puncture was performed that showed an elevated opening pressure of >55 cm H2O. Her headache did not improve with medical management, and the patient eventually underwent ONS fenestration.

Fig. 5 MRI (magnetic resonance imaging) of the brain with contrast showing edema and diffusion restriction in the bilateral optic papillae, more significantly in the right eye.

Fig. 5 MRI (magnetic resonance imaging) of the brain with contrast showing edema and diffusion restriction in the bilateral optic papillae, more significantly in the right eye.

Discussion

Papilledema refers to optic disc swelling because of raised ICP. 3 MRI is the commonly used noninvasive diagnostic modality to study the optic nerves and other orbital structures.3 Common radiological signs associated with IIH are given in Table 1 3 Brodsky and Vaphiades3 proposed that the presence of posterior scleral flattening and prelaminar enhancement on imaging is a confirmatory finding of IIH in the presence of papilledema.6 The other radiological signs that are associated with IIH, however, are nonspecific.3 4 5 6 In our study, we present high T2-weighted signal changes in the optic disc head along with restriction of diffusion as a potential new radiological marker in cases of IIH, and this finding suggests optic nerve ischemia in these patients.

Table 1
Common radiological signs with IIH

Imaging findings

Sensitivity (%)

Specificity (%)

Empty sella

80

83

Meningocele/meningoencephalocele

11

0

Foramen ovale widening

50

80

Posterior flattening of the posterior poles

66

98

Optic nerve head protrusion

36

99

Distention of the optic nerve sheath

58

89

Vertical tortuosity of the optic nerve

43

90

Transverse sinus stenosis

97

93

Enhancement of the optic nerve head

17

99

Tonsillar herniation > 5 mm

16

95

The sensitivity of transverse sinus stenosis was reported to be approximately 90% in patients with IIH.7 Three patients in our case series had a dedicated imaging for the venous system. Among them, one patient had hypoplastic left transverse sinus, and the venous system was unremarkable in all other patients. Two patients did not have venogram, but MRI of the brain with contrast did not show any suggestion of venous sinus occlusion. Sari et al reported that MRI of the brain with contrast is highly sensitive for studying the venous system when compared with MR venogram and noncontrast imaging of the brain.7

All the patients in our case series underwent lumbar puncture, and the opening pressure was >25 mm H2O. These findings are concordant with the opening pressure reported in patients with IIH for the diagnosis.8

The first case of IIH was reported in the 1890s by a German physician Heinrich Quincke, who called it “serous meningitis.”9 Subsequently, Nonne and Dandy reported similar case series of increased ICP without tumor and coined the name “pseudotumor cerebri.”10 11

The reported incidence of IIH in the general population is between 1 and 3 per 100,000 per year, with a higher incidence in females (up to 12 to 28 per 100,000 per year) during their reproductive years.12 13 14 Clinical features of this condition include headache, transient visual obscurations, diplopia, and pulsatile tinnitus. In untreated cases, vision loss is a major complication and sometimes can be very profound within a few days. In a recent study from the United Kingdom, the annual incidence of blindness in patients with IIH is 1 to 2%.15 Friedman proposed diagnostic criteria for IIH that include both patients with and those without papilledema,16 and all of the patients in this case series fulfill those diagnostic criteria. The management of these patients is based on preserving the visual function along with reducing the disability from headache. The treatment options include weight loss in conjunction with medications such as acetazolamide, topiramate, furosemide, and, sometimes, corticosteroids. If the medical therapy fails, the surgical options include serial lumbar punctures, ONS fenestration, ventriculoperitoneal shunt, lumboperitoneal shunt, and transverse sinus stenting. Studies have shown that surgical interventions are effective in improving visual symptoms, preventing vision loss and reducing the morbidity associated with headache.9 15 16

The pathophysiology of IIH and papilledema is still controversial, and the exact mechanism is not clear. The subarachnoid space underneath the ONS is in direct anatomical connection with cerebrospinal fluid (CSF) surrounding the brain. Increased ICP causes a direct transmission of this pressure, resulting in distention of the ONS, as shown in Fig. 6A B, The increase in ICP causes an enlargement of the ONS diameter and changes in tortuosity. This process eventually leads to alteration in the metabolic processes of the nerve and subsequent edema, ischemia, and, finally, visual impairment or loss.3 17 T2-weighted images are used for the analysis of orbital structures and the optic sheath.18 Most of the optic nerve findings are reported from thin-section or volumetric fat-saturated T2-weighted images of the orbit.19 In our series, in addition to all reported findings from the literature, we found increased T2-weighted signal changes in the optic disc head and diffusion restriction. We propose that continued pressure on the optic nerves would result in ischemic insult in the optic nerve head. In ischemic stroke, diffusion sequence on brain MRI shows increased signal with a low ADC signal, and these are the same MRI findings in our case series. To our knowledge, MRI findings involving optic disc heads have not been described in IIH. Given the paucity of specific radiological features in cases of IIH, we propose that the diffusion restriction in the optic disc heads in a patient with clinically suggestive IIH may be considered a fairly specific finding.

Fig. 6 (A) Anatomy of the optic nerve and the central retinal artery and vein present in the center at normal pressure. (B) Compression of both the central retinal artery and vein during raised intracranial pressure.

Fig. 6 (A) Anatomy of the optic nerve and the central retinal artery and vein present in the center at normal pressure. (B) Compression of both the central retinal artery and vein during raised intracranial pressure.

Conclusion

IIH is a headache syndrome that can result in visual deficits including permanent vision loss if left untreated. Diagnosis of this condition relies on proper clinical history and physical examination findings along with measurement of CSF pressure. The finding of a unilateral or bilateral MR diffusion restriction of optical heads in IIH patients has the potential to become a new IIH diagnostic marker if it is confirmed in larger and controlled series. We propose that diffusion restriction in the optic disc heads in the appropriate clinical picture may be a specific radiological finding of IIH.

Note

This study was approved by the Institutional Board Review of the University of Missouri Health Care- Columbia.

Conflict of Interest

None declared.

Funding None.

References

  1. , , , , . The prevalence and burden of migraine and severe headache in the United States: updated statistics from government health surveillance studies. Headache. 2015;55(1):21-34.
    [Google Scholar]
  2. , , , . The diagnosis and management of idiopathic intracranial hypertension and the associated headache. Ther Adv Neurol Disorder. 2016;9(4):317-326.
    [Google Scholar]
  3. , , , , , , . Brain imaging in idiopathic intracranial hypertension. J Neuroophthalmol. 2015;35(4):400-411.
    [Google Scholar]
  4. , , , , , . Magnetic resonance imaging changes in idiopathic intracranial hypertension in children. J Child Neurol. 2010;25(3):294-299.
    [Google Scholar]
  5. , , , , , . Idiopathic intracranial hypertension: the validity of cross-sectional neuroimaging signs. Neuroradiology. 2006;48(8):521-527.
    [Google Scholar]
  6. , , . Magnetic resonance imaging in pseudotumor cerebri. Ophthalmology. 1998;105(9):1686-1693.
    [Google Scholar]
  7. , , , et al . MRI diagnosis of dural sinus - cortical venous thrombosis: immediate post-contrast 3D GRE T1-weighted imaging versus unenhanced MR venography and conventional MR sequences. Clin Neurol Neurosurg. 2015;134:44-54.
    [Google Scholar]
  8. , , . Cerebrospinal fluid pressure in normal obese subjects and patients with pseudotumor cerebri. Neurology. 1983;33(10):1386-1388.
    [Google Scholar]
  9. , , , , , , . Evolving evidence in adult idiopathic intracranial hypertension: pathophysiology and management. J Neurol Neurosurg Psychiatry. 2016;87(9):982-992.
    [Google Scholar]
  10. , . Über Fälle vom Symptomkomplex ‘tumor cerebri’ mit Ausgang in Heilung (Pseudotumor cerebri). Über Letal Verlaufene Fälle von ‘Pseudotumor Cerebri’ mit Sektionsbefund. Dtsch Z Nervenheilkd. 1904;27:169-216.
    [Google Scholar]
  11. , . Intracranial pressure without brain tumor: diagnosis and treatment. Ann Surg. 1937;106(4):492-513.
    [Google Scholar]
  12. , , , , , . Epidemiology of idiopathic intracranial hypertension: a prospective and case-control study. J Neurol Sci. 1993;116(1):18-28.
    [Google Scholar]
  13. , , , , . Idiopathic intracranial hypertension in the Northwest of Northern Ireland: epidemiology and clinical management. Neuroepidemiology. 2015;45(1):34-39.
    [Google Scholar]
  14. , , , . Idiopathic intracranial hypertension and obesity. Horm Res Paediatr. 2014;81(4):217-225.
    [Google Scholar]
  15. , , , , , . The incidence of blindness due to idiopathic intracranial hypertension in the UK. Open Ophthalmol J. 2013;7:26-29.
    [Google Scholar]
  16. , . The pseudotumor cerebri syndrome. Neurol Clin. 2014;32(2):363-396.
    [Google Scholar]
  17. , , , et al . Imaging and interventions in idiopathic intracranial hypertension: a pictorial essay. Indian J Radiol Imaging. 2015;25(4):439-444.
    [Google Scholar]
  18. , , . Using MRI of the optic nerve sheath to detect elevated intracranial pressure. Crit Care. 2008;12(5):181.
    [Google Scholar]
  19. , , . Imaging of intracranial pressure disorders. Neurosurgery. 2017;80(3):341-354.
    [Google Scholar]
Show Sections