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A CASE OF INTRACRANIAL RHABDOMYOSARCOMA Kanji Takemi 1 , Masakazu Ikeda 1 , Kazuo Kimura 2 , Takeshi Yonezawa 3 1Department of Neurosurgery 2Department of Pathology, Kyoto Second Red Cross Hospital 3Department of Pathology, Kyoto Prefectural University of Medicine pp.971-976
Published Date 1977/9/1
DOI https://doi.org/10.11477/mf.1406204130
  • Abstract
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This paper reports a case of a 6 year old boywith rhabdomyosarcoma (RMS) involving thecentral nervous system (CNS). The boy underwentleft mastoidectomy for the presumptive diagnosisof chronic otitis media previously, with resultanthearing loss. The resected polypoid granulationtissue was not investigated histologically. Duringthe postoperative course, the child developed thesymptoms simulating the left Gradenigo's syndrome,followed by the left oculomotor palsy, right hemi-paresis, dysphasia, and deterioration of sensoriumin a rather rapid succession. The carotid angio-gram at this stage revealed a marked stenosis andstretching at the C4-C5 portion of the left internalcarotid artery and a tumor stain within the leftmiddle fossa fed by the external carotid artery.Biopsy taken from the extradural mass at the floorof the left middle fossa gave a histological impres-sion of RMS. The local Co60 irradiation (150 Rsingle tumor dosis × 20 times to the left middlefossa) and systemic administration of Vincristine-Endoxan-Prednisolone combination (VEP therapy)were employed. Upon completion of the radiationtherapy, the boy became alert, regained speechfunction, and the sensori-motor functions weremarkedly improved, though his vision on botheyes became progressively impaired and the palsyof the left III, IV, V and VI cranial nerves persisted.Repeated carotid angiogram at this stage revealedrecanalization of the carotid artery and disap-pearance of the tumor stain. After being well inthis condition for 2 months, the clinical course wasterminated by the sudden loss of consciousness,followed by respiratory paralysis. The entireclinical course was 7 months from the onset of"otitis media". Autopsy findings presented astriking effect of Co60 radiation therapy. Thetumor had been eradicated from the field of irra-diation in the left middle fossa. Outside the fieldof irradiation, however, there were a solid infil-trating tumor occupying the left cerebellopontineangle, the extensive subarachnoid tumor spread inthe form of enveloping the medulla and entirespinal cord, and an isolated metastatic focus in theright frontal white matter. The optic nerves wereheavily infiltrated by the tumor. Tumor tissuesobtained at autopsy were histologically identicalwith the biopsy specimen. The tumor was con-sidered to have originated from the left middleear.

Histological findings of this tumor were describedand the histological diagnostic category of theRMS was discussed with reference to the literature.

Therapeutic evaluation was reviewed. On thebasis of autopsy findings, the systemic VEP therapywas appreciated as practically ineffective, whilethis tumor was found very sensitive to the radi-ation therapy. In view of the characteristicallyextensive spread of the tumor to the subarachnoidspace, the authors are of opinion that the earlytotal CNS irradiation is the treatment of choicefor this particular tumor.


Copyright © 1977, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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