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淋巴瘤样肉芽肿病。光镜、电镜及免疫组化研究。

Lymphomatoid granulomatosis. Light microscopic, electron microscopic and immunohistochemical study.

作者信息

Minase T, Ogasawara M, Kikuchi T, Hirai H, Suzuki A, Nishio C, Ogawa K, Kikuchi K, Mori M

出版信息

Acta Pathol Jpn. 1985 May;35(3):711-21. doi: 10.1111/j.1440-1827.1985.tb00612.x.

Abstract

A case of lymphomatoid granulomatosis (LYG) involving the lungs, skin, stomach, and possibly the left kidney in a 60-year-old man is presented. The infiltrates in the lungs, stomach, and skin showed a polymorphic appearance, and consisted predominantly of lymphocytes of mature and blastic form and of a few neutrophils, plasma cells, and histiocytes. Most lymphoid cells showed irregularly shaped nuclei and clustered dense bodies, characteristics indicative of T lymphocytes. An immunohistochemical study confirmed the T cell origin of the lymphocytes; i.e. they were positive for Leu-1, Leu-3a and Ia-like antigens but negative for Leu-2a antigen and the antibodies against light chains. The homogeneity of the major population of infiltrates in LYG indicates that at least some forms of LYG may be neoplastic or pre-neoplastic lymphocytic disorders which may ultimately progress to malignant lymphoma.

摘要

本文报告一例60岁男性患有的淋巴瘤样肉芽肿病(LYG),病变累及肺、皮肤、胃,可能还累及左肾。肺、胃和皮肤中的浸润灶呈现多形性外观,主要由成熟和母细胞样形态的淋巴细胞以及少量中性粒细胞、浆细胞和组织细胞组成。大多数淋巴细胞显示核形状不规则且有密集的聚集体,这些特征表明是T淋巴细胞。免疫组织化学研究证实了淋巴细胞的T细胞起源;即它们对Leu-1、Leu-3a和Ia样抗原有反应,但对Leu-2a抗原和轻链抗体无反应。LYG中主要浸润细胞群体的同质性表明,至少某些形式的LYG可能是肿瘤性或肿瘤前淋巴细胞疾病,最终可能发展为恶性淋巴瘤。

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