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Extranodal Marginal Zone Lymphoma of the Dura: A Case Report Masahiko YAMADA 1 , Kazuho HIRAHARA 1 , Tetsuzou TOMOSUGI 1 , Takeshi ISHII 1 , Ayumu TANIGUCHI 1 , Yousuke NISHIMUTA 1 , Dan KAWAHARA 1 , Yuko SADAMURA 1 , Kouichi UETSUHARA 1 , Kazunori SUEYOSHI 2 , Yukie TASHIRO 3 , Tadashi YOSHINO 4 , Masayoshi FUJII 4 1Department of Neurosurgery, Kagoshima City Hospital 2Department of Pathology, Kagoshima City Hospital 3Department of Pathology, Imakiire General Hospital 4Department of Pathology, Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Keyword: MALT lymphoma , extranodal marginal zone lymphoma , dural lymphoma , radiation , meningioma , IgG4-positive pp.1079-1085
Published Date 2012/12/10
DOI https://doi.org/10.11477/mf.1436101885
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 The authors present the case of a 65-year-old woman who initially was diagnosed as having intracranial dural B-cell malignant lymphoma. She survived more than 9 years after surgery and radiation. We re-examined the specimens pathologically. Histological findings confirmed an extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT) that showed numerous IgG4-positive plasma cells. MALT lymphomas are already recognized as a distinct clinico-pathological entity. A primary dural MALT lymphoma is very rare and has a favorable clinical outcome, and patients are expected to have an excellent long-term survival with local therapy alone.


Copyright © 2012, 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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