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Chondroblastoma of the temporal bone:a case report Jun SHIMIZU 1 , Nobuyoshi KAITO 1 , Youichi AKIBA 1 , Yoshiji OKUDA 1 , Kouichi TASHIBU 1 , Toshiaki ABE 1 , Shinichiro USHIGOME 2 1Department of Neurosurgery, The Jikei University School of Medicine 2Department of Pathology, The Jikei University School of Medicine Keyword: chondroblastoma , temporal bone , eosinophilic granuloma , giant cell tumor , irradiation pp.555-559
Published Date 1997/6/10
DOI https://doi.org/10.11477/mf.1436901407

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  • Abstract
  • Look Inside

A 30-year-old male had been suffering from left tern-poralgia of six months duration and then developed left hearing disturbance. Craniogram and bone window CT revealed a well defined osteolytic lesion in the left tem-poral bone. CT scan showed an expansile heterogenous mass with calcification. Both Ti and T2 weighted MRI demonstrated a well lobulated mixed intensity mass, but no evidence of dural or intracranial invasion. The tumor exhibited homogenous enhancement on CT and MRI. Angiogram revealed a well marked staining sup-plied by the left middle meningeal and deep temporal arteries. Subtotal removal of the tumor was carried out with cranioplasty. Histologically, this tumor was com-posed of round or polygonal chondroblasts, scattered osteoclast-like giant cells with a foci of cartilage in the stroma. Many reports describe giant cell tumor can be differentiated by immunohistochemical demonstration of S100 protein. Although in our case, histological find-ings simulated those of eosinophilic granuloma, it was diagnosed as chondroblastoma because of the foci of cartilage in the stroma. Because this tumor is usually benign, recurrence of the tumor is rare after surgical re-section. Post-operative irradiation has been reported to be effective in decreasing the recurrence of the tumor. But it should be carefully observed because of possible sarcomatous change in such tumors.


Copyright © 1997, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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