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Hypothalamic Histiocytosis X:Report of a case Yukihiro IBAYASHI 1 , Osamu SATO 1 , Haruhiko HOTTA 1 , Teiji UEDE 1 , Fumikatsu SOHMA 1 1Department of Neurosurgery, Sapporo Medical College Keyword: Hypothalamus , Histiocytosis X , CT , Diagnosis , Treatment pp.395-401
Published Date 1983/4/10
DOI https://doi.org/10.11477/mf.1436201658
  • Abstract
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Histiocytosis X is a non-neoplastic disorder of un-known etiology characterized by a mass of pro-liferating histocytes, plasma cells and inflammatory cells forming a eranuloma within the reticuloendo-thelial elements of any organ system in the body. The three clinical syndromes of this condition, eosinophilic granuloma, Hand-Schüller-Christian disease and Letterer-Siwe disease were unified into a single noso-logical entity by Lichtenstein in 1953. The com-plication of the central nervous system is shown in the cerebrum, cerebellum, sella turcica, hypothalamus and so on.


Copyright © 1983, 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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