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具有早期蕈样肉芽肿组织病理学特征的孤立性皮肤病变。

Solitary skin lesions with histopathologic features of early mycosis fungoides.

作者信息

Cerroni L, Fink-Puches R, El-Shabrawi-Caelen L, Soyer H P, LeBoit P E, Kerl H

机构信息

Department of Dermatology, University of Graz, Austria.

出版信息

Am J Dermatopathol. 1999 Dec;21(6):518-24. doi: 10.1097/00000372-199912000-00003.

Abstract

Mycosis fungoides (MF) is a cutaneous T-cell lymphoma that usually begins with cutaneous patches that evolve into plaques and tumors. A few recent reports describe a solitary variant of MF distinct from localized pagetoid reticulosis, a disease in which solitary verrucous lesions occur on acral skin. Solitary skin lesions with some of the histopathologic features of MF rarely occur during treatment with several drugs, especially antidepressants or antihistamines. We analyzed the clinicopathologic features of 20 patients with solitary skin lesions showing histopathologic features of patch- or early plaque-stage MF. Eight men and 12 women (mean age 50.6, range 23-82, median 49) had solitary, small erythematous patches or plaques located on the trunk (16 cases, 6 of them on the breast), upper extremities (3 cases), and inguinal region (1 case). Ten patients were treated with one or more drugs; only two of them received antidepressants or antihistamines. Histopathologic examination revealed in all cases a band-like infiltrate in the upper dermis, frequently with epidermotropism of solitary lymphocytes. Atypical lymphocytes were present in a minority of cases. Immunohistology showed a predominance of CD3+ T lymphocytes, in most cases admixed with clusters of CD20+ B-cells. Only a small proportion of the infiltrate was CD8+. Molecular analysis of the rearrangement of the T-cell receptor genes was performed in 16 cases using the polymerase chain reaction (PCR) technique and revealed a monoclonal band in 8 of them. After surgical excision, 2/14 patients had a recurrence near the surgical scar. In 18 patients with complete follow-up data, no evidence of "classic" MF could be observed after a mean follow-up of 31.9 months. Solitary skin lesions with the histopathologic features of MF can be considered as a distinct clinicopathologic entity, probably representing a solitary variant of mycosis fungoides.

摘要

蕈样肉芽肿(MF)是一种皮肤T细胞淋巴瘤,通常始于皮肤斑块,随后发展为斑块和肿瘤。最近有一些报告描述了MF的一种孤立性变体,它与局限性派杰样网状细胞增生症不同,后者是一种在肢端皮肤出现孤立性疣状病变的疾病。在使用多种药物治疗期间,尤其是抗抑郁药或抗组胺药时,很少出现具有MF某些组织病理学特征的孤立性皮肤病变。我们分析了20例具有斑片或早期斑块期MF组织病理学特征的孤立性皮肤病变患者的临床病理特征。8名男性和12名女性(平均年龄50.6岁,范围23 - 82岁,中位数49岁)有孤立性、小的红斑性斑片或斑块,位于躯干(16例,其中6例在乳房)、上肢(3例)和腹股沟区(1例)。10例患者接受了一种或多种药物治疗;其中只有2例接受了抗抑郁药或抗组胺药。组织病理学检查在所有病例中均显示真皮上层有条带状浸润,常有单个淋巴细胞向表皮浸润。少数病例存在非典型淋巴细胞。免疫组织化学显示CD3 + T淋巴细胞占优势,大多数病例中混有CD20 + B细胞簇。浸润细胞中只有一小部分是CD8 +。使用聚合酶链反应(PCR)技术对16例患者进行了T细胞受体基因重排的分子分析,其中8例显示单克隆条带。手术切除后,14例患者中有2例在手术瘢痕附近复发。在18例有完整随访数据的患者中,平均随访31.9个月后未观察到“经典”MF的证据。具有MF组织病理学特征的孤立性皮肤病变可被视为一种独特的临床病理实体,可能代表蕈样肉芽肿的一种孤立性变体。

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