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原发性脑淋巴瘤。关于23例的解剖临床、超微结构及免疫细胞化学研究(作者译)

[Primary brain lymphomas. Anatomoclinical, ultrastructural and immunocytochemical study about 23 cases (author's transl)].

作者信息

Hassoun J, Andrac L, Gambarelli D, Toga M

出版信息

Ann Pathol. 1981;1(3):193-203.

PMID:6796097
Abstract

Twenty-three cases of primary brain lymphomas were morphologically studied. Electron microscopy was done in twelve cases and immunoperoxidase reactions for light chains of immunoglobulins in ten cases. The patients were fourteen males and nine females. Except two children, the mean age was 50 years. Clinical features and pre-operative investigations lacked any specificity. Post-operative radiotherapy could be performed in thirteen patients, eleven of them being still alive with a follow-up varying from 2,5 months to 4,5 years. All the other patients persued fulminating course (max: 4,5 months). Tumors were preferentially located in frontal and temporal lobes. On gross examination, well limited tumors were more frequent than ill-defined or purely infiltrating tumors. Microscopically, all the lymphomas were of the diffuse type. Perivascular clusters of lymphoma cells, meningeal and parenchymal infiltrates and sub-ependymal sprouts were found in the peritumoral areas. The lymphomas were cytologically characterized according to the modified Kiel classification (Lennert et al, 1975) using light and electron microscopic data. So were identified thirteen lymphoblastic lymphomas (with one convoluted-cell type), one centroblastic lymphoma, eight immunoblastic lymphomas (two with plasmacytic differentiation). Light chains of human immunoglobulins were immunocytologically demonstrated in six of twelve tumors tested, all the positive cases corresponding to immunoblastic lymphomas. A unique case of primary meningeal Hodgkin's disease was found. These results were compared with the rare previous reports associating these different morphological investigations.

摘要

对23例原发性脑淋巴瘤进行了形态学研究。12例进行了电子显微镜检查,10例进行了免疫球蛋白轻链的免疫过氧化物酶反应。患者中男性14例,女性9例。除2名儿童外,平均年龄为50岁。临床特征和术前检查缺乏特异性。13例患者可进行术后放疗,其中11例仍存活,随访时间从2.5个月至4.5年不等。所有其他患者病情呈暴发性发展(最长4.5个月)。肿瘤多位于额叶和颞叶。大体检查时,边界清楚的肿瘤比边界不清或单纯浸润性肿瘤更常见。显微镜下,所有淋巴瘤均为弥漫型。在肿瘤周围区域发现了淋巴瘤细胞的血管周围聚集、脑膜和实质浸润以及室管膜下芽生。根据改良的基尔分类法(Lennert等人,1975年),利用光镜和电镜数据对淋巴瘤进行细胞形态学特征分析。据此确定了13例淋巴母细胞淋巴瘤(其中1例为卷曲细胞型)、1例中心母细胞淋巴瘤、8例免疫母细胞淋巴瘤(其中2例有浆细胞分化)。在检测的12例肿瘤中的6例中免疫细胞化学显示了人类免疫球蛋白的轻链,所有阳性病例均为免疫母细胞淋巴瘤。发现了1例原发性脑膜霍奇金病的独特病例。将这些结果与以往有关这些不同形态学研究的罕见报告进行了比较。

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Lymphomatoid granulomatosis involving the central nervous system: complication of a renal transplant with terminal monoclonal B-cell proliferation.
Acta Neuropathol. 1983;61(2):141-7. doi: 10.1007/BF00697394.
2
Non-Hodgkin's lymphoma involving the brain. Diagnostic usefulness of stereotactic needle biopsy in combination with paraffin-section immunohistochemistry.累及脑的非霍奇金淋巴瘤。立体定向针吸活检联合石蜡切片免疫组化的诊断价值。
Acta Neuropathol. 1989;78(5):462-71. doi: 10.1007/BF00687707.
3
Diagnosis of primary cerebral lymphoma with particular reference to CT-guided stereotactic biopsy.
Virchows Arch A Pathol Anat Histopathol. 1990;417(1):21-8. doi: 10.1007/BF01600105.
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Primary central nervous system lymphomas--an update.原发性中枢神经系统淋巴瘤——最新进展
J Cancer Res Clin Oncol. 1992;119(1):7-27. doi: 10.1007/BF01209483.