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Neurology India, Vol. 51, No. 2, April-June, 2003, pp. 263-265 Case Report Simultaneous occurrence of multiple meningiomas in different neuraxial compartments H. S. Bhatoe Accepted on 18.10.2001. Code Number: ni03082 ABSTRACT The simultaneous occurrence of multiple meningiomas in different neuraxial compartments is rare. A 35-year-old female patient had multiple meningiomas involving both the supratentorial compartments and in the upper dorsal spine. The patient underwent excision of 2 cranial and 2 spinal meningiomas, and has remained asymptomatic over a follow-up period of 18 months. Key Words: Supratentorial, Multiple meningioma, Spinal tumor. The term multiple meningioma is used to describe the simultaneous or sequential appearance of 2 or more independently situated meningiomas, not necessarily of the same pathologic subtype. In the pre-CT (computed tomography) era, the frequency of multiple meningiomas without neurofibromatosis was reported to be less than 3%.1,2 Since the introduction of CT scan, the frequency of multiple meningiomas has ranged between 4.5% and 10.5%.3,4 Nevertheless, the concomitant occurrence of multiple intracranial and spinal (S) meningiomas in the same patient is rare. A case having 4 meningiomas is reported. CASE REPORT A 35-year-old female patient had a three-month history of generalized headaches and progressive stiffness and weakness of all four limbs. She had no stigmata of neurofibromatosis. On examination, she had bilateral papilloedema, left-sided lower motor neuron type facial paresis and sensorineural hearing impairment. There was spastic grade 3-4 quadriparesis. T1 and T2 weighted magnetic resonance imaging (MRI) showed an isointense mass in the left infratentorial-cerebellopontine angle. Contrast enhanced MRI revealed small multiple meningiomas over the parietal parasagittal and convexity regions on both sides and a large meningioma arising from the tentorium (Figures 1a & 1b). MRI spine showed two isointense tumors on T1& T2 at D1 & D3 region, one lying ventral and the other lying dorsal to the cord, sandwiching the cord between them (Figure 2). The spinal tumors were excised initially and 4 days later, the left tentorial meningioma was resected by left temporal craniotomy. After 2 weeks, a nodular parasagittal vertex meningioma was excised. Following the surgeries, she showed symptomatic improvement. Histological examination of the 2 spinal meningiomas revealed atypical and fibroblastic meningioma respectively. The tentorial meningioma was of the transitional variety, while the parasagittal tumor was a meningothelial meningioma. At a follow-up after 18 months, she is asymptomatic. DISCUSSION Multiple meningiomas were first described by Anfimow and Blumenau.5 Cushing and Eisenhardt2 classified them as a discrete clinical entity. Multiple meningiomas were associated with neurofibromatosis.6 However, the current concept is that these tumors are due to inherent multicentricity of the dural foci, possibly influenced by hormonal factors.7 The incidence of multiple intracranial meningiomas in the post-CT era has been reported to be between 5.4 and 8.9%, while the incidence as seen in autopsy series is between 8.2 and 16.9 %. The majority of these are located in a hemicranial distribution.3,8 Multiple spinal meningiomas are rarer than multiple cranial (C) meningiomas.9 Multiple meningiomas occurring in different neuraxial compartments are distinctly rare, with only 17 well-documented cases reported in world literature (Table 1). Only 4 of these occurred in males (M:F-1:4), out of which 2 were children. The relationship between isolated multiple meningiomas and neurofibromatosis is unsettled. In cases with reported cranial and spinal meningiomas, 5 (27.77%) had more than 1 intracranial tumor10-13 and only 2 reports (mentioned earlier)14,15 had more than 1 spinal tumor. Operative management of multiple meningiomas occupying both cranial and spinal compartments poses special problems. A decision is made regarding which lesion, or lesions should be removed initially. Small or asymptomatic tumors may be followed up with serial imaging. Histologically, each of these tumors may be a different variant of meningioma. REFERENCES 1. Abtahi H. Multiple Meningiomas. Acta Neurochir 1975;31:279. (Proceedings).
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