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[蕈样肉芽肿。6例患者的临床特征及治疗]

[Mycosis fungoides. Clinical characteristics and treatment of 6 patients].

作者信息

Dotterud L K, Aarstein K, Falk E S

机构信息

Hudavdelingen Regionsykehuset i Tromsø.

出版信息

Tidsskr Nor Laegeforen. 1991 Jun 10;111(15):1850-2.

PMID:1853318
Abstract

Mycosis fungoides is a low grade malignant cutaneous T-cell lymphoma. It is a rare disorder where diagnosis may be difficult to establish in early stages. Usually several years may pass between onset of disease and confirmation of the diagnosis, which should be confirmed histopathologically. Prognosis is difficult to predict and depends on whether mycosis fungoides is limited to the skin or has spread to lymph nodes or viscera. Based on the confirmation of six new cases of mycosis fungoides during the last 18 months by the Department of Dermatology, University Hospital of Tromsø, we discuss clinicopathological findings and alternative methods of treatment.

摘要

蕈样肉芽肿是一种低度恶性的皮肤T细胞淋巴瘤。这是一种罕见的疾病,早期诊断可能很难确立。通常在疾病发作和确诊之间可能会经过数年时间,确诊应通过组织病理学检查来确认。预后难以预测,这取决于蕈样肉芽肿是局限于皮肤还是已扩散至淋巴结或内脏。基于特罗姆瑟大学医院皮肤科在过去18个月中确诊的6例蕈样肉芽肿新病例,我们讨论了临床病理表现及替代治疗方法。

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