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MALT-type Lymphoma of Lacrimal Gland: Case Report Masato SAKA 1 , Jun MORIOKA 1 , Koji KAJIWARA 1 , Koichi YOSHIKAWA 1 , Takayuki AMANO 1 , Hisashi KUBOTA 1 , Sadahiro NOMURA 1 , Syoichi KATO 1 , Masami FUJII 1 , Hirosuke FUJISAWA 1 , Michiyasu SUZUKI 1 1Department of Neurosurgery,Yamaguchi University School of Medicine Keyword: lacrimal gland , lymphoma , MALT , orbita pp.475-479
Published Date 2007/5/10
DOI https://doi.org/10.11477/mf.1436100527
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 A 72-year-old female presented with a lump in the left superior-lateral eyelid. The magnetic resonance imaging showed a well-delineated mass in the left lacrimal gland. The tumor was isointense on both the T1 and T2 weighted images, and it was homogenously enhanced with Gd-DTPA. Surgery via the trans-cranial approach revealed a pinkish and elastic-hard tumor. Total resection was successfully performed. The hematoxilyn-eosin staining of the surgical specimen showed a dense infiltrate of lymphocytes, which were composed predominantly of small lymphocytes, centrocyte-like cells, monocytoid cells, and occasionally transformed lymphocytes. The immunohistochemical findings for CD20, CD3, UCHL-1, CD23, CD5, cyclinD1, and bcl-2 were compatible with Mucosa Associated Lymphoid Tissue (MALT)-type lymphoma. The patient received local radiation therapy (30Gy / 15 fractions). She remained in complete clinical remission of the disease about one and a half years after treatment.


Copyright © 2007, 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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