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蕈样肉芽肿:临床病程及细胞异常

Mycosis fungoides: clinical course and cellular abnormalities.

作者信息

Epstein E H

出版信息

J Invest Dermatol. 1980 Jul;75(1):103-6. doi: 10.1111/1523-1747.ep12521312.

Abstract

Mycosis fungoides is a lymphoma that appears to begin in skin. Although variable in its clinical course, it tends to affect middle-aged people, is present for a median of 4 yr before diagnosis, and generally results in death of the patient 4 to 5 yr after diagnosis. Cutaneous tumors and palpably enlarged lymph nodes are associated with shortened survival, and each of these frequently is accompanied by extracutaneous dissemination of the disease. The malignant cells are T lymphocytes with highly infolded nuclei, and they frequently express a helper cell function. Their chromosome complement has been found to be abnormal in karyotyping studies, and measurement of the amount of DNA by cytophotometry may permit diagnosis of the disease before the histological characteristics are detectable by light microscopy.

摘要

蕈样肉芽肿是一种似乎起源于皮肤的淋巴瘤。尽管其临床病程多变,但它倾向于影响中年人,在诊断前平均存在4年,并且通常在诊断后4至5年导致患者死亡。皮肤肿瘤和可触及的肿大淋巴结与生存期缩短相关,并且这些情况中的每一种都经常伴有疾病的皮肤外播散。恶性细胞是具有高度折叠核的T淋巴细胞,并且它们经常表达辅助细胞功能。在核型分析研究中发现它们的染色体组是异常的,并且通过细胞光度术测量DNA量可能在通过光学显微镜可检测到组织学特征之前就能诊断该疾病。

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