Simultaneous trigonal and spinal meningioma with varied histology: A rare case report

Abstract

Background:

Meningioma is one of the most common neoplasms of the central nervous system. Multiple meningiomas without neurofibromatosis are not a usual occurrence. Intraventricular meningioma with spinal meningioma is rare and not been reported in the literature.

Case Description:

We report a case of a 63-year-old male with the left trigonal and spinal meningioma. Both the meningiomas were resected in different settings. The histological examination of tumors revealed to be of varied histology, that is, meningothelial and atypical meningioma, respectively.

Conclusion:

Although various cases with multiple cranial and spinal meningiomas are described, this is the first case of an intraventricular and spinal meningioma. With varied histology, the case also reaffirms the theory of polyclonal origin of multiple meningiomas.

INTRODUCTION

Meningiomas are tumors of the covering of the brain. These are the most common non-glial primary brain tumors, which constitute almost 37% of all primary intracranial neoplasms and 53% of non-malignant tumors.[11] In these tumors’, subset of meningiomas arising within the ventricles is rare with constituting only about 0.5–5% of all intracranial tumors.[5] Spinal meningiomas constitute of 25% of all spinal tumors.[12] Multiple meningiomas occurring along the neuraxis are quite uncommon in absence of neurofibromatosis. Although some cases with simultaneous intracranial and spinal meningiomas have been seldom reported, no case with simultaneous intraventricular and spinal meningioma has been reported. We hereby present such a case in absence of neurofibromatosis.

CASE REPORT

A 63-year-old male presented complaints of weakness in bilateral lower limbs left more than right, paraesthesia in bilateral lower limbs and difficulty in walking from past 5 months. On examination, patient was found to have increased tone in bilateral lower limbs and power of 4/5(MRC grading) in bilateral lower limbs. Patient also had reduced touch and pain sensation below eighth thoracic dermatome level. Bladder function and sphincter control were preserved.

MRI demonstrated a T1 hypointense and T2 hyperintense and contrasts enhancing intradural extramedullary lesion at eighth thoracic level. Contrast MRI of the brain revealed a 4.2 × 3.6 × 3.5 cm lesion in the trigonal area of the left lateral ventricle. The lesion was T1 hypointense and heterogeneously contrasts enhancing [Figure 1].

Figure 1:

MRI brain showing 4.2 × 3.6 × 3.5 cm T2 heterogenous (a and b) lesion with contrast Enhancement (d and e). MRI brain with gadolinium demonstrating enhancing intradural Extramedullary lesion at 8^th thoracic level.

Patient, due to his symptoms of the spinal lesion underwent excision of the spinal lesion. D7 and D8 laminectomy was performed. Tumor was dorsal placed and total excision along with attached dura was performed. Dural defect was closed and wound closed with a drain in situ. Patient’s spasticity and gait improved in the postoperative period. Patient complained of headache in the postoperative period and hence MRI brain was performed. The cranial lesion was planned for a second stage surgery since patient did not exhibit any symptom for the same.

On follow-up patient presented to us with two episodes of seizures, 2 months after the spinal surgery and patient was admitted for excision of the cranial component. The left parietal craniotomy was performed and trigone was approached through the keens point. Excision was performed and patient had an uneventful postoperative course.

Microscopic examination of the spinal tumor showed a meningothelial neoplasm having transitional morphology. The cells were moderately pleomorphic and were arranged in fascicles, whorls, and lobules with few psammoma bodies. The tumor had mitotic activity reaching upto 4/10hpf and a Ki-67 labeling index of 12–15%. Due to the increased mitotic count, this tumor was classified as atypical meningioma, the WHO Grade II [Figure 2].

Figure 2:

Meningioma excised from D8 spinal level showing features of atypical meningioma, WHO Grade II with increased mitotic activity (a, mitotic figures marked by arrows) and elevated Ki-67 labelling index. In contrast, the neoplasm excised from trigone exhibits morphological features of transitional meningioma, WHO Grade I with low Ki-67 labelling index (d). (a and c) Haematoxylin and eosin; (b and d) Immunoperoxidase; Magnification=scale bar (a-d: 20 μm)

Resected tissue from the trigone showed a meningothelial neoplasm exhibiting transitional morphology with few psammoma bodies, lymphocytic, and foamy macrophage infiltration. The cells were arranged in fascicles and whorls and had moderate nuclear pleomorphism, mitotic activity of 1–2/10hpf and Ki-67 labeling index of 4–5%. There was no evidence of brain parenchymal invasion. These features were of a transitional meningioma, the WHO Grade I.

DISCUSSION

Anifimow and Blumenau were the first to report multiple meningiomas as early as 1889.[1]

Meningiomas are called multiple when they occur as at least two in the neuraxis spatially separated and at the same time or more than two arising sequentially from two distinct regions.[14] Incidence of multiple meningiomas has been described between 5.4% and 8.9% and these have mostly been cranial in distribution.[3] Occurrence of multiple meningiomas in the cranial and spinal axis in the setting of neurofibromatosis 2 has been very common. However, there are only few case reports of occurrence of multiple cranial and spinal meningiomas without neurofibromatosis 2. There have been seven cases described in the literature with multiple cranial and spinal meningiomas in patients devoid of neurofibromatosis 2 mutation.

Meningiomas are a frequent occurrence in NF2 found in about half of the patients. NF2 is usually the disease in young people when they have multiple meningiomas. However, adults with multiple meningiomas but no vestibular schwannomas are highly unlikely to be affected by neurofibromatosis 2.[6]

Intraventricular meningiomas are a rare variant and constitute of only about 0.5–5% of all intracranial meningiomas.[10] They usually present late or even are diagnosed incidentally. These tumors are thought to arise from either from mesenchymal stromatolites of choroid plexus or from nests of arachnoid cell nest tissue within the choroid plexus.[8]

Pathogenesis of multiple meningiomas has been tried to explain in two theories. The two theories are: (1) either these arise independently as proven by differences seen in the histological or cytogenic differences between the tumors themselves. (2) One transforming event and clone cells spread throughout the meninges leading to the development of clonally related multiple tumors.

Female preponderance is a usual observation in meningiomas. This stands true in case of intraventricular meningiomas, that is, 2:1[9] and also in reported cases of multiple cranial and spinal meningiomas with four female patients in comparison to only two male patients. Our patient was a 58-year-old male hence making it a rare occurrence. In the most instances of multiple tumors, it is the spinal component which becomes symptomatic in the form of spasticity, difficulty in walking, weakness, and rarely bowel bladder involvement. They tend to present late. Our patient was asymptomatic but later presented with seizures which are common for a meningioma but has been seldom a presenting feature in an intraventricular meningioma.

Operative management of multiple meningiomas has remained unsettled for a long period now. Which tumor to operated first and when to operate has posed a serious dilemma? Not all tumors in case of multiple meningiomas need to be operated. Resection of multiple intracranial and spinal meningiomas has been reported. Intraventricular meningiomas are very different in the way of management than their supratentorial counterparts.

Atypical meningiomas have a recurrence rate of 29–38% of cases.[4] Total surgical resection remains the treatment of choice. However, role of radiotherapy in the management of spinal meningiomas is controversial due to possible damage by the radiation per se.[15] Gezen et al.[7] treated meningiomas with radiotherapy as an adjuvant treatment after total or subtotal resection. Although, an imaging follow-up would be advisable in these patients with yearly MRI for a period of 5 years.

The majority of multiple meningiomas described in the literature are benign. Moreover, in case of spinal multiple meningiomas psammomatous variant predominates. Histologically, case described by Sedzimir et al.[13] where only spinal component was psammomatous variant. Bhatoe[2] observed that the four resected tumors by them had four different histological variants, that is, transitional, meningothelial, fibroblastic, and atypical. Our case had meningiomas with two different histological variants I.e. transitional and atypical variant intracranially and spinal respectively as in the case reported by Bhatoe et al. Our case differs in this aspect also that the most spinal tumors in case of multiple meningiomas are psammomatous variant whereas ours was an atypical variant which in itself is a rare occurrence in the spinal cord.

Thus, reaffirming one of the theories of the pathogenesis stated that these tumors arise independently and are clonally different tumors. Elderly age, male sex, and histology make our case a unique one in the literature.

CONCLUSION

Multiple meningiomas along the neuraxis and intraventricular meningiomas are both rare entities. Multiple meningiomas in the absence of NF2 are a rare entity but should be kept in mind always in case of varied clinical manifestations. Two histological variants of meningioma in cranium and spine are a proof of the origin of meningioma through polyclonal cells. Atypical meningiomas (the WHO Grade 2) are extremely rare in spinal canal and will warrant a complete resection and close follow-up.

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Conflicts of interest

There are no conflicts of interest.