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SOLITARY RETICULOGRANULOMA OF THE SKULL Hiroshi ABE 1 , Kenzo YADA 1 , Mitsuo TSURU 1 1Dept. of Nevrosurgery, Hokkaido Univ. School of Med. pp.29-34
Published Date 1965/1/1
DOI https://doi.org/10.11477/mf.1406201759
  • Abstract
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Although in most of the cases clinical features have distinct characteristics, eosinophilic granuloma, Hand-Schuller-Christian's disease and Letterer-Siwe's disease have in recent years grouped together on the bases of similar pathologic findings as manifestations of reticuloendotheliosis at different stages of the disease.

As we found in Japanese literature only several cases of solitary reticuloendotheliotic lesion confined to the skull, we report four such cases treated at the Department of Neurosurgery, Hokkaido University Hospital during the past 5 years.

There were one male and three females, age ranging from 11 to 28 years. The initial symptoms were localized pain and swelling of the scalp over the skull lesions. Two of the patients gave a history of traumatic injury on or about the skull lesions. The lesions were located in the frontal bone in two of the cases, one in the parietal bone, and one was in the occipital bone.

Radiological examinations revealed a well localized punched out single lesion in all the cases.

In order to establish definitive diagnosis, all the cases were treated surgically. After taking biopsy, the lesions were curettaged and the bone edges were rongeured.

Histological examination revealed a typical eosino-philic granuloma in three of the cases and Hand-Schuller-Christian's disease in another.


Copyright © 1965, 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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