|Year : 2016 | Volume
| Issue : 3 | Page : 374-376
Postoperative posterior ischemic optic neuropathy (PION) following right pterional meningioma surgery
Boby Varkey Maramattom1, Shyam Sundar2, Dalvin Thomas2, Dilip Panikar2
1 Department of Neurology, Aster Medcity, Kochi, Kerala, India
2 Department of Neurosurgery, Aster Medcity, Kochi, Kerala, India
|Date of Submission||13-Apr-2015|
|Date of Decision||08-Sep-2015|
|Date of Acceptance||08-Sep-2015|
|Date of Web Publication||25-Jul-2016|
Boby Varkey Maramattom
Department of Neurology, Aster Medcity, Cheranelloor, Kochi 23, Kerala
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Postoperative visual loss (POVL) is an unpredictable complication of nonocular surgeries. Posterior ischemic optic neuropathy (PION) is particularly feared in spinal surgeries in the prone position. We report a rare case of PION occurring after surgery for a pterional meningioma and discuss the various factors implicated in POVL.
Keywords: PION, Post op blindness, meningioma and PION
|How to cite this article:|
Maramattom BV, Sundar S, Thomas D, Panikar D. Postoperative posterior ischemic optic neuropathy (PION) following right pterional meningioma surgery. Ann Indian Acad Neurol 2016;19:374-6
|How to cite this URL:|
Maramattom BV, Sundar S, Thomas D, Panikar D. Postoperative posterior ischemic optic neuropathy (PION) following right pterional meningioma surgery. Ann Indian Acad Neurol [serial online] 2016 [cited 2019 Nov 22];19:374-6. Available from: http://www.annalsofian.org/text.asp?2016/19/3/374/186826
| Introduction|| |
Postoperative visual loss (POVL) occurring in nonocular surgeries is a catastrophe with poor prognosis in most cases.  The main causes are ischemic optic neuropathies [anterior ischemic optic neuropathy (AION) or posterior ischemic optic neuropathy (PION)], central retinal artery occlusion (CRAO), pituitary apoplexy, and occipital infarction. The risk has been estimated to be around 0.013-0.2% and is higher for spinal surgeries.  PION is more common with spinal surgeries or radical neck dissections, whereas AION is more common with cardiac surgeries. We present a case of PION occurring after nonocular surgery (pterional meningioma excision).
| Case Report|| |
A 56-year-old man was admitted for elective surgery for an incidental right pterional meningioma. The meningioma was detected when he underwent neuroimaging for anosmia [Figure 1]. On examination, there were no focal deficits and visual acuity and fields were normal. Preoperative routine investigations were within normal limits. He underwent a right pterional incision in the supine position with head tilt to the left side with excision of tumor (Simpsons grade 2 excision) under general anesthesia (GA). Intraoperatively, there was an extraxial lesion seen in the pterional region with attachment to the dura overlying the lateral sphenoid wing, with feeders from the middle meningeal artery. There was no well-defined plane of cleavage from the surrounding brain parenchyma except at some areas in the sylvian fissure. A bone flap was raised and the sphenoid wing was drilled to open the superior orbital fissure. The dura was opened and the tumor was gently decompressed. A small part of the tumor, which was adherent to sylvian vessels was left behind. Hemostasis was attained and the dura was closed with the pericranium and fascia lata. He was extubated within hours of the surgery and started following commands. Overnight, he complained of painless loss of vision in the right eye. On examination, there was a right afferent papillary defect and absence of light perception in the right eye. Emergent computed tomography (CT) of the brain showed only postoperative tumor bed changes. Magnetic resonance image (MRI) showed diffusion restriction in the right-sided intraorbital segment of the optic nerve (ON). The intraorbital segment of the right ON appeared hyperintense and slightly edematous. The optic chiasm appeared normal. MRA source images clearly demonstrated a patent right ophthalmic artery till the mid-intraorbital optic nerve. There were postoperative changes with hemosiderin staining and minimal mass effect on the right side with a midline shift of 3 mm [Figure 2]. The MRI findings were consistent with a right-sided PION with optic nerve infarction. Visual evoked potentials showed absent potentials from the right eye. Fundoscopy on day 5 was normal. He was started on intravenous (IV) methylprednisolone 1 g/day over 5 days. At discharge 1 week later, he had not regained light perception in the right eye.
|Figure 1: Panel A. Preoperative MRI showing a right pterional meningioma. Panel B shows a preoperative DWMRI with normal optic nerves. Panel C. DWMRI showing diffusion restriction in the right ON. Panel D. ADC images showing reduced ADC in the right ON. Panel E. MRI MIP images showing a patent's right ophthalmic artery. Panel F. Postoperative CT showing minimal postoperative changes|
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| Discussion|| |
POVL with nonocular surgery is a feared and unforeseeable complication [Table 1]. Numerous causes are associated with POVL and practice advisories to offset this catastrophe have been enumerated by societies [Table 2]. PION has been most associated with spine surgery in the prone position; postulated to be due to factors such as increased orbital venous pressure, direct ocular pressure, or increased intraocular pressure. During radical neck dissection, ligation of the internal jugular veins is postulated to lead to distension of ophthalmic veins and compression of the orbital apex with ischemia of the posterior optic nerve (ON). 
|Table 1: Perioperative and intraoperative factors associated with nonocular surgery-related visual loss|
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The peculiarities in the blood supply of the ON result in various clinical presentations. The optic nerve head (ONH) is supplied by the short posterior ciliary arteries (PCAs), which arise from the ophthalmic artery.  Moreover, the blood vessels at the ONH anterior to the lamina cribrosa are exposed to the intraocular pressure and posteriorly to the cerebrospinal fluid pressure. The rest of the ON has a dual vascular supply system; a peripheral centripetal system via the pial branches of the ophthalmic artery and a central core centrifugal system via branches of the central retinal artery (CRA) [Figure 3]. These branches sometimes extend 1-4 mm posterior to the site of penetration of the CRA into the ON. Hence, the ON is more vulnerable to ischemia than the ONH as it is supplied through easily compressible centripetal pial vessels.
Although AION can be diagnosed by fundoscopy, the diagnosis of PION is often delayed as fundoscopy is normal. Recent reports have demonstrated the utility of MRI in PION, showing diffusion restriction in the ON with decreased apparent diffusion coefficient (ADC) indicating ischemic injury. ,
At present, preoperative evaluation cannot identify patients at risk of POVL. Nevertheless, it is prudent to inform patients of the small risk of POVL if prolonged surgery or substantial blood loss is anticipated. Postoperative visual assessment should be performed in all high-risk patients. If visual loss is identified, urgent ophthalmologic evaluation can help to determine the etiology [Table 2]. Currently, there is no role for the use of antiplatelets, steroids, or intraocular pressure-lowering agents in POVL although it is beneficial to optimize hemoglobin values, hemodynamic status, and arterial oxygenation parameters. MRI is helpful in establishing the etiology of POVL.
| Conclusion|| |
In conclusion, our patient had PION based on the normal fundoscopic exam and MRI appearance of diffusion restriction in the ON. Our patient did not have any perioperative risk factors; hence, our postulation is that a sudden decrease in intracranial pressure during dural opening could have led to altered perfusion of the ON and PION. POVL and PION can occur postoperatively even in the absence of established risk factors. 
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Conflicts of interest
There are no conflicts of interest.
| References|| |
Buono LM, Foroozan R. Perioperative posterior ischemic optic neuropathy: Review of the literature. Surv Ophthalmol 2005;50: 15-26.
Berg KT, Harrison AR, Lee MS. Perioperative visual loss in ocular and nonocular surgery. Clin Ophthalmol 2010;24:531-46.
Marks SC, Jaques DA, Hirata RM, Saunders JR Jr. Blindness following bilateral radical neck dissection. Head Neck 1990;12: 342-5.
Hayreh SS. Ischaemic optic neuropathy. Indian J Ophthalmol 2000;48:171-94.
Al-Shafai LS, Mikulis DJ. Diffusion MR imaging in a case of acute ischemic optic neuropathy. AJNR Am J Neuroradiol 2006;27: 255-7.
Srinivasan S, Moorthy S, Sreekumar K, Kulkarni C. Diffusion-weighted MRI in acute posterior ischemic optic neuropathy. Indian J Radiol Imaging 2012;22:106-7.
Deutch D, Lewis RA. Intraocular pressure after cardiopulmonary bypass surgery. Am J Ophthalmol 1989;107:18-22.
Purvin V, Kuzma B. Intraorbital optic nerve signal hyperintensity on magnetic resonance imaging sequences in perioperative hypotensive ischemic optic neuropathy. J Neuroophthalmol 2005;25:202-4.
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2]