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模拟恶性肿瘤的乳腺颗粒细胞瘤。两例病例的光镜、透射电镜及免疫组化研究报告。

Granular cell tumour of the mammary gland simulating malignancy. A report on two cases with light microscopy, transmission electron microscopy and immunohistochemical investigation.

作者信息

Willén R, Willén H, Balldin G, Albrechtsson U

出版信息

Virchows Arch A Pathol Anat Histopathol. 1984;403(4):391-400. doi: 10.1007/BF00737288.

Abstract

Primary granular cell tumours of the breast in 35 and 55 year old women were studied by light microscopy, transmission electron microscopy and immunohistochemistry. Light and electron microscopy revealed a neural origin of the tumours and this was further substantiated by immunohistochemical studies, with positive S-100 protein reaction and negative reactions for surface heavy and light chains, CEA, alfa-1-antitrypsin, muramidase and GFA-protein. Granular cell tumour of the mammary gland is a very rare tumour. Clinically it sometimes simulates carcinoma because of its fibrous consistency, fixation to pectoral fascia and skin retraction. The diagnosis of granular cell tumour should be included in the differential diagnosis of carcinoma of the breast. The granular cell tumour is derived from neuro-ectodermal tissue. Whether it represents a neurogenic cell-confined metabolic disturbance with lysosomal activation, or a true neoplasm remains to be elucidated.

摘要

对35岁和55岁女性的乳腺原发性颗粒细胞瘤进行了光镜、透射电镜和免疫组织化学研究。光镜和电镜显示肿瘤起源于神经,免疫组织化学研究进一步证实了这一点,S-100蛋白反应阳性,而表面重链和轻链、癌胚抗原、α-1抗胰蛋白酶、溶菌酶和神经胶质纤维酸性蛋白反应阴性。乳腺颗粒细胞瘤是一种非常罕见的肿瘤。临床上,由于其纤维质地、与胸肌筋膜固定以及皮肤回缩,它有时会模拟癌。乳腺颗粒细胞瘤的诊断应列入乳腺癌的鉴别诊断中。颗粒细胞瘤起源于神经外胚层组织。它是代表一种伴有溶酶体激活的神经源性细胞局限性代谢紊乱,还是一种真正的肿瘤,仍有待阐明。

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