A Case of Cutaneous Meningioma in the Rudimentary Meningocele.

Q4 Medicine Hiroshima journal of medical sciences Pub Date : 2016-03-01
Junichiro Ochiai, Satoshi Yamaguchi, Masaaki Takeda, Rupendra Bahadur Adhikari, Manish Kolakshyapati, Vega Karlowee, Kazuhiko Sugiyama, Kaoru Kurisu
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Abstract

We report a rare case of neonatal cutaneous meningioma derived from a rudimentary meningocele. This neonate had a congenital skin-covered hump in the thoracolumbar region. Computed tomography showed bifid laminae of T12 and L1 underneath the mass lesion. Magnetic resonance images showed the mass to have no cerebrospinal fluid space and that it had a stalk connecting to the spinal canal. Split cord malformation was also observed under the bifid laminae. Because of the increasing size of the lump and cosmetic reasons, the parents opted for surgical treatment. We operated on the patient 9 months after birth. Operative findings showed that the cutaneous mass was connected to intraspinal contents by a vascular stalk and it was totally removed. The split spinal cord was untouched. The histopathological findings of the mass showed components of meningioma with a collagenous matrix. We concluded that this patient had a meningioma derived from rudimentary meningocele.

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原发性脑膜膨出的皮肤脑膜瘤1例。
我们报告一例罕见的新生儿皮肤脑膜瘤源自初级脑膜膨出。这个新生儿在胸腰椎区域有一个先天性的皮肤覆盖的驼峰。计算机断层扫描显示肿块病变下方的T12和L1双裂层。磁共振图像显示肿块没有脑脊液空间,有一柄与椎管相连。在两裂椎板下也观察到劈裂脊髓畸形。由于肿块越来越大和美容的原因,父母选择了手术治疗。我们在病人出生9个月后给他做了手术。手术结果显示皮肤肿块通过血管柄与椎管内内容物连接,并被完全切除。断裂的脊髓未受影响。肿块的组织病理学结果显示脑膜瘤成分与胶原基质。我们的结论是,这名患者有脑膜瘤源自初级脑膜膨出。
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Hiroshima journal of medical sciences
Hiroshima journal of medical sciences Medicine-Medicine (all)
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0.30
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