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21例原发性中枢神经系统淋巴瘤的临床病理研究

[A clinicopathological study of 21 cases of primary central nervous system lymphoma].

作者信息

Nitta T, Kasuga C, Yasumoto Y, Okuda O, Kudo S, Sato K

机构信息

Department of Neurosurgery, Juntendo University School of Medicine.

出版信息

No Shinkei Geka. 1994 Sep;22(9):827-32.

PMID:8090264
Abstract

A clinico-pathological study was carried out in 21 cases of primary central nervous system-non-Hodgkin's lymphoma (CNS-NHL). Their clinical profiles (age, prognosis, modalities of treatment) and findings of radio-imaging were analyzed. All specimens from surgery and/or autopsy were histologically classified according to the working formulation (WF) classification of the National Cancer Institute. Ontogeny of lymphoma cells was determined by immunohistochemical study in all cases and some cases were subjected to light (kappa, lambda) and heavy chain (IgG, IgA, IgM) analysis as well. Among 21 cases, 12 cases were located in the cerebral hemisphere, 7 in the thalamus-basal ganglia and 4 in the cerebellum. Radio-imaging study showed that 18 cases (86%) revealed isodensity mass lesions on plain CT, which were homogeneously enhanced by contrast medium. The pathological study showed that all cases were derived from B-cells. Five were classified as immunoblastic type (IBL), 9 as diffuse large type (DL), and the others were classified according to WF. 17 of 21 cases (81%) were sensitive to radiotherapy, and 15 of 19 cases (79%) responded to corticosteroid. A prognostic study revealed that patients with IBL had less hope than those with DL. From this result, it seems that WF classification is better than LSG classification for obtaining a prognosis in malignant lymphoma patients. The frequency of primary CNS-NHL has been increasing for the past several decades and will surpass that of any other brain tumors in the near future because of the explosive expansion of AIDS patients. Therefore, not only clinicopathological analysis but also biological study for CNS-NHL might be important.

摘要

对21例原发性中枢神经系统非霍奇金淋巴瘤(CNS-NHL)患者进行了临床病理研究。分析了他们的临床特征(年龄、预后、治疗方式)以及影像学检查结果。所有手术和/或尸检标本均按照美国国立癌症研究所的工作分类法(WF分类)进行组织学分类。所有病例均通过免疫组化研究确定淋巴瘤细胞的起源,部分病例还进行了轻链(κ、λ)和重链(IgG、IgA、IgM)分析。21例患者中,12例位于大脑半球,7例位于丘脑-基底节,4例位于小脑。影像学研究显示,18例(86%)在CT平扫上表现为等密度肿块,增强扫描后呈均匀强化。病理研究表明,所有病例均来源于B细胞。5例为免疫母细胞型(IBL),9例为弥漫大B细胞型(DL),其余病例按照WF分类。21例中有17例(81%)对放疗敏感,19例中有15例(79%)对皮质类固醇有反应。预后研究表明,IBL患者的预后比DL患者差。由此结果看来,在预测恶性淋巴瘤患者的预后方面,WF分类比LSG分类更好。在过去几十年中,原发性CNS-NHL的发病率一直在上升,由于艾滋病患者数量的急剧增加,在不久的将来其发病率将超过任何其他脑肿瘤。因此,不仅对CNS-NHL进行临床病理分析,而且进行生物学研究可能都很重要。

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