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伴有脑受累的淋巴瘤样肉芽肿病。一例病例的光镜和电镜研究

Lymphomatoid granulomatosis with cerebral involvement. Light and electron microscopic study of a case.

作者信息

Peña C E

出版信息

Acta Neuropathol. 1977 Mar 31;37(3):193-7. doi: 10.1007/BF00686878.

Abstract

Light and EM study of a case of lymphomatoid granulomatosis revealed a pleomorphic lymphoreticular cell infiltrate, angitis and necrosis with involvement of the brain, lungs, skin and right ear of a 30 year old woman. Cells comprising the infiltrate were classified as lymphocytoid, plasmacytoid, immunoblastic (histocytic) and phagocytic. A number of elements partook of the ultrastructural features of two cell types and were considered to be intermediate forms (plasmacytoid lymphocytes, lymphocytoid immunoblasts, and plasmacytoid immunoblasts). It is believed that the various cell elements form part of a wide spectrum in which transformation of cell types takes place by maturation. This suggests an immunologic process as the main pathogenetic factor in the development of LG.

摘要

对一例淋巴瘤样肉芽肿病的光学显微镜和电子显微镜研究显示,一名30岁女性的脑、肺、皮肤和右耳出现多形性淋巴网状细胞浸润、血管炎和坏死。构成浸润的细胞被分类为淋巴细胞样、浆细胞样、免疫母细胞(组织细胞样)和吞噬细胞。一些细胞成分具有两种细胞类型的超微结构特征,被认为是中间形式(浆细胞样淋巴细胞、淋巴细胞样免疫母细胞和浆细胞样免疫母细胞)。据信,各种细胞成分构成了一个广泛的谱系,其中细胞类型通过成熟发生转化。这表明免疫过程是淋巴瘤样肉芽肿病发生发展的主要致病因素。

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