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ISSN: 2329-6895

Journal of Neurological Disorders
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Case Report

A Pediatric Case of Solitary Myofibroma

Yukihiro Goto*, Hiroyasu Sasajima, Yuichi Furuno, Takuya Kawabe, Kei Ohwada, Kazunori Tatsuzawa, and Naoya Hashimoto
Department of Neurosurgery, Kyoto Prefectural University, Graduate School of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, 602-8566, Japan
*Corresponding Author : Yukihiro Goto
Department of Neurosurgery, Kyoto Prefectural University
Graduate School of Medicine, Kawaramachi-Hirokoji
Kamigyo-ku, Kyoto, 602-8566, Japan
Tel: 81752515541
Fax: 81752515544
E-mail: [email protected]
Received date: February 05, 2016; Accepted date: March 22, 2016; Published date: March 25, 2016
Citation: Goto Y, Sasajima H, Furuno Y, Kawabe T, Ohwada K, et al. (2016) A Pediatric Case of Solitary Myofibroma. J Neurol Disord 4:263. doi:10.4172/2329-6895.1000263
Copyright: © 2016 Goto Y, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

A 5-year-old male was referred to our department for evaluation of a firm elastic mass at the back of his head. Clinical examination revealed no abnormalities but the local area was tender. Further clinical and radiological examinations yielded no pathological findings and no other lesions were detected. The lesion was located in the diploic layer of the left parietal bone. The inner layer of the skull intact but the outer layer showed osteolytic change. The lesion did not adhere to the dura mater. The tumor was completely removed with the surrounding bone. Histological examination revealed a mesenchymal tumor comprised of myoid spindle-shaped cells arranged in whorls between muscle cells and fibroblasts and a vascular component around the spindle cells. The final diagnosis was myofibroma. The patient recovered well after the operation and he was discharged from hospital 10 days after surgery. Clinical and radiological follow-up 6 and 12 months later showed neither recurrence of the primary lesion nor any indications of lesions at other sites. Myofibroma is a benign neoplasm composed of myoid cells with thin-walled blood vessels. This tumor, reported to have a wide range of clinical manifestations, is one of the cranial vault tumors. These tumors occur mainly in children although a few affected infants have been reported. Surgical intervention may contribute significantly to the diagnosis of solitary myofibroma and complete removal achieves good outcomes. Herein, we report a 5-year-old male with solitary myofibroma of the skull, presenting as a firm elastic mass in the left parietal bone.

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