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Primary Spinal Intramedullary Malignant Lymphoma:Case report Koji NAKAO 1 , Shiro WAGA 1 , Hiroshi SAKAIDA 1 , Makoto SAKAKURA 2 , Hiroshi TOCHIO 2 , Hidekazu OHNO 2 , Masao MIYAZAKI 3 1Department of Neurosurgery, Mie University School of Medicine 2Department of Neurosurgery, Yamada Red Cross Hospital 3Department of Neurology, Yamada Red Cross Hospital Keyword: Intramedullary tumor , Malignant lymphoma , Spinal cord tumor pp.583-587
Published Date 1994/6/10
DOI https://doi.org/10.11477/mf.1436900860
  • Abstract
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We report a case of primary spinal intramedullary malignant lymphoma.

A 48-year-old man suffered from numbness and weakness of the left leg for 8 months. He was admitted to the hospital with progressive paraplegia and sudden onset of urinary retention. MRI revealed a low intensity mass on T1-weighted image with diffuse enhancement by Gd-DTPA in the thoracic spinal cord. An in-tramedullary spinal cord tumor was suspected and an urgent laminectomy (C7-Th5) was performed for de-compression and confirmation. In the operation, the spinal cord was seen to be diffusely swollen, but no apparent tumor was identified either in color or con-sistency, and only biopsy was performed. The patholo-gical diagnosis was malignant lymphoma (diffuse medium size-cell type) . Investigations excluded the pre-sence of lymphoma in other sites in the central nervous system and in the extraneural organs. We diagnosed a primary spinal intramedullary malignant lymphoma. Postoperative irradiation and chemotherapy were per-formed. After the irradiation with 16Gy to the tumor and 30Gy to the whole spinal axis, the tumor dis-appeared on MRI. One month later MRI demonstrated two markedly enhanced lesions in the right frontal lobe white mantle and the corpus callosum. He died of pro-gressive respiratory disturbance 15 months after the be-ginning of his illness. Primary involvement of the spinal cord in malignant lymphoma is rare. Only 12 cases have been reported. The number of cases of malignant lymphoma in the central nervous system has gradually increased and it must be taken into consideration when diagnosing spinal cord tumors. We are looking forward to developing curative means including chemotherapy and radiotherapy.


Copyright © 1994, 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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