Case Reports in Orthopedics

Case Reports in Orthopedics / 2021 / Article

Case Report | Open Access

Volume 2021 |Article ID 6651160 | https://doi.org/10.1155/2021/6651160

Shunsuke Ito, Yoichi Iizuka, Masanori Aihara, Hiromi Koshi, Tokue Mieda, Eiji Takasawa, Sho Ishiwata, Yusuke Tomomatsu, Akira Honda, Kazuhiro Inomata, Hirotaka Chikuda, "Angiomatous Meningioma in the Craniocervical Junction", Case Reports in Orthopedics, vol. 2021, Article ID 6651160, 5 pages, 2021. https://doi.org/10.1155/2021/6651160

Angiomatous Meningioma in the Craniocervical Junction

Academic Editor: Da sen Li
Received18 Dec 2020
Revised28 Mar 2021
Accepted01 Apr 2021
Published12 Apr 2021

Abstract

Introduction. Spinal angiomatous meningioma arising in the craniocervical junction has not been reported. Case Presentation. A 68-year-old man presented to our hospital with pain in the back and left leg. He showed slight motor weakness in his upper extremities. Magnetic resonance imaging revealed a mass with marked enhancement in the craniocervical junction. Computed tomography angiography showed feeding vessels arising from the right vertebral artery. Preoperative embolization of the feeding vessels was performed to reduce intraoperative bleeding. Gross total resection of the tumor was achieved by debulking and piecemeal resection. The tumor attachment to the dura mater was also resected (Simpson grade 1 resection). A histopathological examination confirmed the diagnosis of an angiomatous meningioma. The patient’s symptoms improved shortly after surgery. Conclusions. We achieved gross total resection of spinal angiomatous meningioma arising in the craniocervical junction. A preoperative evaluation and embolization of the feeding arteries may help prevent massive intraoperative bleeding.

1. Introduction

Angiomatous meningioma, characterized by an abundant vascular component, is a rare subtype of meningioma, accounting for 2.1% of meningiomas [1]. Angiomatous meningiomas arising from the spinal cord is even rarer. We herein report a case of angiomatous meningioma in the craniocervical junction.

2. Case Presentation

A 68-year-old man without notable comorbidity presented to our hospital with a 15-month history of pain in the back and left leg. A neurological examination revealed motor weakness (manual muscle testing 4 out of 5) in the upper extremities. Magnetic resonance imaging (MRI) demonstrated an intradural mass lesion at the craniocervical junction, which has low intensity on both T1- and T2-weighted imaging. Enhanced MRI with gadolinium-diethylenetriaminepentaacetic acid (Gd-DTPA) showed homogeneous enhancement without a dural tail sign (Figure 1). Computed tomography angiography using iodinated contrast agent revealed two feeding vessels arising from the right vertebral artery.

Given the aggravating symptoms, the patient decided to undergo surgery. To reduce the risk of massive bleeding, we embolized the feeding arteries using soft coils prior to surgery. An angiogram after embolization showed a decreased tumor stain (Figure 2). Subsequently, resection of the tumor was performed the same day. Following durotomy, a tumor mass was identified on the ventrolateral side of the spinal cord. Resection was carefully performed via central debulking with piecemeal resection to avoid neurological damage under spinal monitoring (Figure 3). We observed substantial but manageable bleeding from inside of the tumor. The tumor attachment to the dura mater was also resected (Simpson grade 1 resection). The dural defect was repaired with a Gore-Tex patch and further covered with a bioabsorbable polyglycolic acid sheet and fibrin glue. The intraoperative blood loss, mainly due to bleeding from the tumor itself, was 567 ml. The drain was removed two days after surgery without noticeable cerebrospinal fluid leakage.

A histopathological examination showed numerous blood vessels making up most of the mass and intervening tumor cells. The blood vessels were variably hyalinized and thick-walled. The tumor cells had round nuclei with occasional intranuclear pseudoinclusions. Some whorls and psammoma bodies were present (Figure 4). Immunohistochemically, the tumor cells were positive for epithelial membrane antigen, and the MIB-1 index was <1%. The tumor was diagnosed as an angiomatous meningioma.

The patient’s symptoms, including back pain and leg pain, improved shortly after surgery. MRI obtained one year after surgery revealed decompression of the spinal cord and no sign of recurrence (Figure 5). The patient remained neurologically intact until he died of an unrelated cause 16 months after surgery.

3. Discussion

Spinal angiomatous meningioma is extremely rare. To our knowledge, a total of 16 cases have been reported (Table 1) [26]. Angiomatous meningiomas are classified as WHO grade 1 meningioma without aggressive nature, while motor and/or sensory deficits and bladder and rectal disturbance can occur as the disease progresses. Spinal angiomatous meningiomas arise most commonly in the thoracic spine followed by the cervical spine [26]. The present case is the first report of angiomatous meningioma in the craniocervical junction.


AuthorsAgeSexLocationTreatmentDural attachmentBlood lossFollow-upOutcome

Gul et al. 2008 [2]25FT9-L2GTRNANANANA
Vij et al. 2012 [3]16MC2-C5GTR; piecemeal resectionNANA3 dDead
Wu et al. 2015 [4]28MC2-C3Simpson grade II; piecemeal resectionVentral400152 mNo recurrence
56FC1-C3GTR; en bloc resectionNerve root100131 mNo recurrence
54FT10-T11Simpson grade II; piecemeal resectionVentral500120 mNo recurrence
49MT1-T3Simpson grade I; en bloc resectionDorsal200108 mNo recurrence
43FT1GTR; en bloc resectionNerve root10099 mNo recurrence
28FC2-C4GTR; en bloc resectionNerve root10086 mNo recurrence
67FC7-T3Simpson grade II; en bloc resectionLateral30072 mNo recurrence
76FT4Simpson grade II; en bloc resectionLateral10061 mNo recurrence
41MT11-T12Simpson grade II; en bloc resectionLateral10053 mNo recurrence
54MC1-C2Simpson grade II; piecemeal resectionVentral60032 mNo recurrence
57MT12-L1Simpson grade II; piecemeal resectionLateral40018 mNo recurrence
42MC2-C3Simpson grade II; en bloc resectionLateral20011 mNo recurrence
Yang et al. 2016 [5]55FT6-T8Simpson grade II; en bloc resectionDorsolateralNA6 mNo recurrence
Missori et al. 2017 [6]40MT3-T4GTRNerve rootNA14 mNo recurrence
Present case68MO-C1Simpson grade I; piecemeal resectionVentrolateral56711 mNo recurrence

M: male; F: female; C: cervical; T: thoracic; L: lumbar; GTR: gross total resection; RT: radiotherapy; CT: chemotherapy; NA: not available; d: day; m: month.

The preferable treatment for angiomatous meningioma is Simpson grade 1 resection (total resection including dural attachment and abnormal bone) although some researchers suggested that Simpson grade 2 resection (total resection and dural coagulation) is sufficient [4, 710]. In the present case, we decided to perform Simpson grade 1 resection to reduce risk of potential recurrence. As angiomatous meningiomas are rich in small blood vessels, preoperative embolization to reduce tumor blood supply may be useful [11]. Contrarily, Wu et al. reported good control of intraoperative bleeding without using preoperative embolization. The authors found that en bloc resection was associated with a significant reduction of intraoperative blood loss compared with piece-by-piece resection [4]. In the present case, even though we successfully embolized the feeding arteritis just prior to the surgery, we still observed substantial intraregional bleeding.

When spinal angiomatous meningioma is suspected, we recommend performing a preoperative evaluation of the feeder vessels using an angiogram. Subsequent embolization of the feeder vessels should be discussed, especially when the tumor is located ventrally, making en bloc resection difficult.

Data Availability

There are no available data supporting the results of this study as it is a case report.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

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Copyright © 2021 Shunsuke Ito et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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