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孤立性蕈样肉芽肿:一种具有良好预后的独特临床病理实体:一系列 15 例病例及文献复习。

Solitary mycosis fungoides: a distinct clinicopathologic entity with a good prognosis: a series of 15 cases and literature review.

机构信息

St John's Institute of Dermatology, London, United Kingdom.

出版信息

J Am Acad Dermatol. 2012 Oct;67(4):736-44. doi: 10.1016/j.jaad.2012.02.039. Epub 2012 Apr 24.

Abstract

BACKGROUND

Mycosis fungoides (MF) is the most common cutaneous T-cell lymphoma (CTCL), accounting for almost 50% of all primary cutaneous lymphomas. The occurrence of solitary lesions, which are clinically and histopathologically indistinguishable from classic MF has been described.

OBJECTIVE

We describe 15 cases of solitary MF and discuss the relationship to classic MF, "reactive" processes and to other, rarer forms of CTCL that may present with solitary lesions.

METHODS

We conducted a retrospective chart review and a PubMed search to identify all reported cases of solitary MF to date, as well as information about other CTCLs presenting as a solitary lesion.

RESULTS

Fifteen patients were identified. Follow-up data were available on 10 patients with a median follow-up of 10 months (range, 1 to 48 months). Clinical, pathological, immunocytochemical, and molecular-genetic features were analyzed. Five cases were diagnosed as folliculotropic MF (FMF). Of the 10 cases with follow-up, 2 were treated with topical steroids, 2 were completely excised, 5 received radiotherapy, and 1 received tacrolimus. One hundred twenty-eight cases of solitary MF were identified in the literature and reviewed for commonalities to and differences with our cases and other CTCLs.

LIMITATIONS

This study was retrospective; follow-up data were not available in some cases and were only short term in others.

CONCLUSIONS

Solitary MF appears to have a good prognosis. In lesions that are not completely excised, curative radiotherapy can be used. Long-term follow up is advised.

摘要

背景

蕈样肉芽肿(MF)是最常见的皮肤 T 细胞淋巴瘤(CTCL),占所有原发性皮肤淋巴瘤的近 50%。已经描述了临床上和组织病理学上与经典 MF 无法区分的孤立性病变的发生。

目的

我们描述了 15 例孤立性 MF,并讨论了其与经典 MF、“反应性”过程以及其他可能表现为孤立性病变的罕见 CTCL 之间的关系。

方法

我们进行了回顾性图表审查和 PubMed 搜索,以确定迄今为止所有报道的孤立性 MF 病例,以及其他表现为孤立性病变的 CTCL 信息。

结果

确定了 15 名患者。对 10 名患者的随访数据进行了分析,中位随访时间为 10 个月(范围 1 至 48 个月)。分析了临床、病理、免疫细胞化学和分子遗传学特征。5 例诊断为滤泡性 MF(FMF)。在有随访的 10 例中,2 例接受局部皮质类固醇治疗,2 例完全切除,5 例接受放射治疗,1 例接受他克莫司治疗。在文献中确定了 128 例孤立性 MF,并对其与我们的病例和其他 CTCL 的共同点和差异进行了回顾。

局限性

本研究为回顾性研究;在一些病例中没有获得随访数据,在其他病例中仅获得短期随访数据。

结论

孤立性 MF 似乎预后良好。对于未完全切除的病变,可以使用根治性放疗。建议长期随访。

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