Korean J Radiol. 2011 Jul-Aug;12(4):499-503. English.
Published online Jul 22, 2011.
Copyright © 2011 The Korean Society of Radiology
Case Report

Reversal in the Diameter of the Superior Ophthalmic Vein after an Epidural Blood Patch in a Case of Spontaneous Intracranial Hypotension

Chen Yu Hsiao, MD,1 and Yuh Feng Tsai, MD1,2,3
    • 1Department of Diagnostic Radiology, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
    • 2College of Medicine, Fu-Jen Catholic University, New Taipei City, Taiwan.
    • 3Neuroimaging Center, Department of Health Management, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
Received July 22, 2010; Accepted December 07, 2010.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Spontaneous intracranial hypotension (SIH) is caused by single or multiple cerebrospinal fluid (CSF) leaks in the spine with the prototypical symptom of postural headache. One of the characteristic MRI features in SIH is intracranial venous engorgement. This report presents a case of SIH with engorgement of the bilateral superior ophthalmic veins (SOVs) which resume their normal diameters by the third day of successful epidural blood patches (EBPs). We define this phenomenon as the "reversal of the SOV" sign.

Keywords
Blood patch, epidural; Cerebrospinal fluid (CSF); Intracranial hypotension, spontaneous; Magnetic resonance imaging (MRI)

INTRODUCTION

Spontaneous intracranial hypotension (SIH) is rare, with an estimated annual incidence of five per 100,000. The female : male ratio is about 2:1 and the peak incidence is reached at the fourth decade (1). The pathogenesis remains unclear but is thought to be the result of spinal cerebrospinal fluid (CSF) leaks (1). Although a definite diagnosis is made when CSF opening pressure is less than 60 mm H2O at the lumbar puncture (1, 2), some authors have reported that the CSF leaks can be depicted on a MR myelography with the use of a heavily T2-weighted pulse sequence (3, 4). Clinical manifestations in SIH are widely variable with the most characteristic manifestation being a postural headache, which is defined by the revised International Classification of Headache Disorders criteria as a headache occurring or worsening within 15 minutes while assuming the upright position and gradually improving within 15 to 30 minutes after lying down (1, 5). Other commonly related symptoms include a stiff neck, nausea, vomiting, diplopia, cranial neuropathies, and marked exacerbation of the headache by Valsalva maneuver (1, 5). There are multiple available treatment options which include bed rest, analgesics, sedatives, oral caffeine, intravenous hydration, epidural blood patch (EBP), epidural saline infusion, and direct surgical repair of spinal dura tear (1, 6). Among them, the mainstay of treatment is EBP, a procedure to secure a CSF leak that in turn restores brain buoyancy (1). Surgical repair of a dura tear is reserved for a patient with an identifiable site for a CSF leak that is refractory to EBP (1, 4, 7). The majority of patients with SIH have favorable outcomes and the resolution of symptoms may be achieved in a period of weeks and months to years after treatments (1, 8-11). The advent of MRI has revolutionized the understanding of SIH. Typical MR imaging features include subdural collections, dural thickening and pachymeningeal enhancement, engorged venous structures, pituitary hyperemia, and sagging of the brain (1, 12). The superior ophthalmic vein (SOV) drains into the cavernous sinus and is theoretically influenced by the alteration in intracranial pressure. However, the relationship between the SIH and the SOV diameter, before and after EBP, was rarely investigated. Our case demonstrates a striking regression of the SOV diameter three days after an EBP. The "reversal of the SOV" sign is introduced, which implies the reconstruction of intracranial pressure and is also highly suggestive of a successful EBP procedure.

CASE REPORT

A 65-year-old man began to suffer from an intermittent right fronto-parietal headache and right neck soreness seven months prior to admission. The headache, as he described, was not related to his posture. He sought medical help because of the development of an orthostatic headache a few days prior to admission. Brain and spinal MRI studies were performed. The brain MRI revealed dural thickening with pachymeningeal enhancement, subdural effusion, pituitary hyperemia, and a slight brain sag (Fig. 1A, B), which are typical findings of SIH. In addition, bilateral ophthalmic veins were significantly engorged (Fig. 1C). MR myelography, using the heavily T2-weighted pulse sequence, revealed CSF leaks in the thoracic epidural space from the T1 to T6 levels (Fig. 1D, T4 level illustrated). An EBP was performed the next day by injection of 30 c.c. of autologous blood into the T6 epidural space. The patient was kept in the Trendelenburg position for two hours after the procedure to allow for the ascension of blood over several segments towards the sites of CSF leaks. However, he did not experience instantaneous relief of the postural headache. The first follow-up MRI was performed on the third day after the EBP, which showed the complete seal of spinal CSF leaks and a striking reversal of the bilateral SOV diameters (Fig. 1E, F). The second follow-up MRI on the eleventh day after EBP failed to demonstrate any resorption of bilateral subdural collections or regression of dural venous engorgement (Fig. 1G, H). The diameters of the bilateral SOVs were stable (Fig. 1I). The postural headache persisted, but subsided dramatically about one and a half months later. Serial follow-up brain and spinal MRI studies at one-month intervals in the following four months showed gradual resolution of the subdural collections (Fig. 1J) without recurrent spinal CSF leak. Of note, the diameters of the bilateral SOVs were stable without further engorgement.

Fig. 1
Characteristic MR imaging findings of spontaneous intracranial hypotension.

A. Postcontrast coronal T1-weighted image shows thin and uniform thickening of dura and tentorium (long arrows), as well as bilateral subdural effusion (short arrows). B. Postcontrast sagittal T1-weighted image shows enlargement of pituitary gland with diffuse enhancement; so-called pituitary hyperemia (long arrow), and engorgement of superior sagittal sinus, straight sinus and internal cerebral vein, as well as so-called engorgement of venous structures (short arrows). C. Coronal T2-weighted image, obtained day before epidural blood patch after suffering from postural headache for few days, shows significant engorgement of bilateral superior ophthalmic veins (arrows), which measure about 6 mm in diameter on both sides. D. Spinal MR myelography (T2-weighted image, echo time = 750 ms, T4 level) disclosed abnormal fluid accumulation along nerve sheaths (more significant on left side), which is suggestive of cerebrospinal fluid leaks (arrows). E. Coronal T2-weighted image obtained on third day after epidural blood patch shows significant regression of bilateral superior ophthalmic vein diameters (arrows); approximately 2 mm in diameter on both sides compared to 6 mm before procedure. F. Spinal MR myelography shows blockage of cerebrospinal fluid leak. G. Coronal fluid attenuation inversion recovery image obtained on eleventh day after epidural blood patch shows mild dural thickening (short arrows) and persistent bilateral subdural collections without regression (long arrows). H. Sagittal T2-weighted image shows persistent engorgement of superior sagittal sinus, straight sinus, and internal cerebral vein (arrows) without regression. I. Coronal T2-weighted image shows stationary diameters of bilateral superior ophthalmic veins (arrows) without further engorgement. J. Coronal fluid attenuation inversion recovery image obtained about four months later after epidural blood patch shows complete resolution of bilateral subdural collections.

DISCUSSION

The clinical manifestation, typical MRI features, and treatment options in SIH have been well described in the literature (1-12). In this article, we introduce the "reversal of the SOV" sign following the EBP procedure, which we believe may imply the reconstruction of intracranial pressure.

According to the Monroe-Kellie hypothesis, the sum of the volumes of intracranial blood, CSF, and cerebral tissue should be constant in an intact cranium (13). Both the clinical symptoms and MRI features in SIH can be the result of a spinal CSF leak. The postural headache can be explained by CSF volume depletion with loss of CSF buoyancy, which in turns leads to brain sagging and traction of various intracranial pain-sensitive structures (1). For pachymeningeal enhancement, engorgement of the venous structures and pituitary hyperemia could be the results of compensatory effects for increasing the vascular component (1). As for the subdural collection, it is intended for increasing the intracranial CSF component (1).

The majority of CSF is produced by the choroid plexuses in the brain. Circulating over the brain and spinal cord, the CSF provides the supporting buoyancy for the central nervous system. The estimated CSF space is about 160 to 170 mL in a young adult and CSF is produced at a rate of 0.4 mL/min (14). As a result, the turnover rate is about four times a day. Based on this inference, the CSF volume should become normal within one day if the CSF leak has been secured by a successful EBP.

Dural venous engorgement is one of the imaging features in SIH. In one series, the authors observed that 14 of 15 (93%) patients with intracranial hypotension were associated with engorgement of the transverse sinus (15). Since the cavernous sinuses are not completely isolated from the dura matter, they are easily influenced by alteration in intracranial hydrodynamics (16). The SOV, which serves as one of the tributaries of the cavernous sinus and brings the venous flow from the orbit back to the cavernous sinus, is theoretically also influenced by alteration in intracranial hydrodynamics. As can been seen in our case, the diameters of bilateral SOVs had already returned to a normal status before the evolution of other imaging features were perceptible. Therefore, the diameter of SOV may indirectly reflect the status of intracranial pressure.

However, the relationship between the diameter of SOV and the intracranial pressure has been rarely investigated. In one series, the authors measured the average diameter of SOV on MRI and found that it was smaller in SIH where the term, "collapsed" SOV was used to describe this feature (17). In another study, the authors, by color Doppler imaging, found both the mean diameter and the flow of the SOV were substantially greater in SIH (18).

We cannot explain the discrepancy in the aforementioned studies, but our case supports that an engorged SOV might be one of the features of SIH, a mechanism such as an engorged dural vein in SIH. Nevertheless, it remains unclear whether the "reversal of the SOV" in our case definitely implies a complete seal of the CSF leak and restoration of intracranial pressure or whether the finding was incidental. Therefore, further case reports or studies are encouraged to further delve into this phenomenon. It is recommended that Color Doppler imaging be performed to access the diameter of the SOV, because it can be done at bed side without the need for sending the patient to an MRI room, and thus helps to prevent recurrent CSF leaks.

In summary, a high index of clinical suspicion and familiarity with MRI features are essential for a diagnosis of SIH to be made with confidence. Heavily T2-weighted MR myelography can benefit from its non-invasiveness. It is thus worth recommendation, not only for localization of CSF leak, but also for evaluation of post-treatment efficacy. The "reversal of the SOV" sign may provide adjunctive information for knowledge of post-treatment intracranial hemodynamic change. However, the application of "reversal of the SOV" sign to patients with SIH, in whom the SOVs are collapsed, is uncertain and needs substantially greater investigation.

References

    1. Schievink WI. Spontaneous spinal cerebrospinal fluid leaks and intracranial hypotension. JAMA 2006;295:2286–2296.
    1. Mokri B, Krueger BR, Miller GM, Piepgras DG. Meningeal gadolinium enhancement in low pressure headache. Ann Neurol 1991;30:294–295.
    1. Wang YF, Lirng JF, Fuh JL, Hseu SS, Wang SJ. Heavily T2-weighted MR myelography vs CT myelography in spontaneous intracranial hypotension. Neurology 2009;73:1892–1898.
    1. Tsai PH, Fuh JL, Lirng JF, Wang SJ. Heavily T2-weighted MR myelography in patients with spontaneous intracranial hypotension: a case-control study. Cephalalgia 2007;27:929–934.
    1. Headache Classification Subcommittee of the International Headache Society. The International Classification of Headache Disorders: 2nd edition. Cephalalgia 2004;24 Suppl 1:9–160.
    1. Mokri B. Headaches caused by decreased intracranial pressure: diagnosis and management. Curr Opin Neurol 2003;16:319–326.
    1. Schievink WI, Morreale VM, Atkinson JL, Meyer FB, Piepgras DG, Ebersold MJ. Surgical treatment of spontaneous spinal cerebrospinal fluid leaks. J Neurosurg 1998;88:243–246.
    1. Schievink WI, Reimer R, Folger WN. Surgical treatment of spontaneous intracranial hypotension associated with a spinal arachnoid diverticulum. Case report. J Neurosurg 1994;80:736–739.
    1. Franzini A, Messina G, Nazzi V, Mea E, Leone M, Chiapparini L, et al. Spontaneous intracranial hypotension syndrome: a novel speculative physiopathological hypothesis and a novel patch method in a series of 28 consecutive patients. J Neurosurg 2010;112:300–306.
    1. Lai TH, Fuh JL, Lirng JF, Tsai PH, Wang SJ. Subdural haematoma in patients with spontaneous intracranial hypotension. Cephalalgia 2007;27:133–138.
    1. Schievink WI, Maya MM, Moser FG, Tourje J. Spectrum of subdural fluid collections in spontaneous intracranial hypotension. J Neurosurg 2005;103:608–613.
    1. Tosaka M, Sato N, Fujimaki H, Tanaka Y, Kagoshima K, Takahashi A, et al. Diffuse pachymeningeal hyperintensity and subdural effusion/hematoma detected by fluid-attenuated inversion recovery MR imaging in patients with spontaneous intracranial hypotension. AJNR Am J Neuroradiol 2008;29:1164–1170.
    1. Mokri B. The Monro-Kellie hypothesis: applications in CSF volume depletion. Neurology 2001;56:1746–1748.
    1. Silverberg GD, Heit G, Huhn S, Jaffe RA, Chang SD, Bronte-Stewart H, et al. The cerebrospinal fluid production rate is reduced in dementia of the Alzheimer's type. Neurology 2001;57:1763–1766.
    1. Farb RI, Forghani R, Lee SK, Mikulis DJ, Agid R. The venous distension sign: a diagnostic sign of intracranial hypotension at MR imaging of the brain. AJNR Am J Neuroradiol 2007;28:1489–1493.
    1. Spektor S, Piontek E, Umansky F. Orbital venous drainage into the anterior cavernous sinus space: microanatomic relationships. Neurosurgery 1997;40:532–539.
      discussion 539-540.
    1. Chen WT, Fuh JL, Lirng JF, Lu SR, Wu ZA, Wang SJ. Collapsed superior ophthalmic veins in patients with spontaneous intracranial hypotension. Neurology 2003;61:1265–1267.
    1. Chen CC, Luo CL, Wang SJ, Chern CM, Fuh JL, Lin SH, et al. Colour doppler imaging for diagnosis of intracranial hypotension. Lancet 1999;354:826–829.

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