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淋巴瘤样丘疹病合并蕈样肉芽肿:15例病例研究

Lymphomatoid papulosis in association with mycosis fungoides: a study of 15 cases.

作者信息

Basarab T, Fraser-Andrews E A, Orchard G, Whittaker S, Russel-Jones R

机构信息

St John's Institute of Dermatology, St Thomas' Hospital, London, UK.

出版信息

Br J Dermatol. 1998 Oct;139(4):630-8.

PMID:10025972
Abstract

We report clinical findings in 15 patients with lymphomatoid papulosis (LyP) associated with mycosis fungoides (MF). LyP either preceded (n = 4), followed (n = 5) or occurred concurrently with the MF lesions (n = 6). Twenty-eight LyP lesions were classified histologically and analysed further with immunostaining for CD3 and CD30. Five biopsies contained a predominance of type A cells, six biopsies contained a predominance of type B cells. and six were mixed (A + B). However, 11 biopsies contained a population of atypical mononuclear cells with large hyperchromatic nuclei that we have termed indeterminate cells. These cells contained a thin rim of eosinophilic cytoplasm and showed strong CD30 but absent, faint or normal CD3 staining. In seven biopsies from five separate patients these cells represented the predominant cell type and we have termed this the pleomorphic variant of LyP. Analysis of T-cell receptor genes using Southern blot analysis and polymerase chain reaction/single strand conformational polymorphism analysis identified a T-cell clone in six of 16 LyP lesions and nine of 16 MF lesions. In the three patients who had clones in both types of skin lesions, the clones were identical. Only two of 10 blood samples, both of which were from the same patient, had a T-cell clone and none of two lymph nodes showed evidence of a clonal population. To date all patients are alive with a median follow-up of 15 years from the onset of the first lesion. One patient has developed Lin anaplastic large cell lymphoma of the nasopharynx. These data augment the current literature on the association of LyP and MF and suggest that the

摘要

我们报告了15例与蕈样肉芽肿(MF)相关的淋巴瘤样丘疹病(LyP)患者的临床发现。LyP要么先于MF病变出现(4例),要么在MF病变之后出现(5例),要么与MF病变同时发生(6例)。对28个LyP病变进行了组织学分类,并进一步用CD3和CD30免疫染色分析。5份活检标本中以A型细胞为主,6份活检标本中以B型细胞为主,6份为混合型(A + B)。然而,11份活检标本中含有一群非典型单核细胞,其核大、染色质深,我们称之为不确定细胞。这些细胞含有一层薄薄的嗜酸性细胞质边缘,CD30染色强,但CD3染色缺失、微弱或正常。在来自5例不同患者的7份活检标本中,这些细胞是主要细胞类型,我们将其称为LyP的多形性变异型。使用Southern印迹分析和聚合酶链反应/单链构象多态性分析对T细胞受体基因进行分析,在16个LyP病变中的6个和16个MF病变中的9个中鉴定出T细胞克隆。在两种皮肤病变中均有克隆的3例患者中,克隆是相同的。10份血液样本中只有2份(均来自同一患者)有T细胞克隆,2个淋巴结均未显示克隆群体的证据。迄今为止,所有患者均存活,从第一个病变出现开始的中位随访时间为15年。1例患者发生了鼻咽间变性大细胞淋巴瘤。这些数据丰富了目前关于LyP与MF关联的文献,并表明……

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