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在 153 例患者的一系列病例中,蕈样肉芽肿和 CD30 阳性皮肤 T 细胞淋巴瘤增殖患者 T 细胞抗原缺失的发生率。

Prevalence of T-cell antigen losses in mycosis fungoides and CD30-positive cutaneous T-cell lymphoproliferations in a series of 153 patients.

机构信息

Department of Pathology, APHP, Henri Mondor Hospital, Creteil, France.

Department of Dermatology, APHP, Henri Mondor Hospital, Creteil, France; Univ Paris Est Creteil EpiDermE, Creteil, France.

出版信息

Pathology. 2022 Oct;54(6):729-737. doi: 10.1016/j.pathol.2022.02.008. Epub 2022 May 14.

DOI:10.1016/j.pathol.2022.02.008
PMID:35577607
Abstract

Mycosis fungoides (MF) and primary cutaneous CD30-positive T-cell lymphoproliferative disorders (CD30LPD) are the most frequent primary cutaneous T-cell lymphomas. Our objective was to study pan-T-cell antigens and PD-1 expression in a large cohort of MF and CD30LPD with a special interest in antigen losses as a diagnostic tool. We retrospectively reviewed 160 consecutive samples from 153 patients over a 3 year period, including 104 with MF and 49 with CD30LPD. As controls, benign inflammatory dermatoses (BID, n=19) were studied. A semi-quantitative evaluation of CD2, CD3, CD4, CD5, CD7, CD8 expression was performed. PD-1 and double stainings (CD3+CD7 and PD-1+CD7) were performed in a subset of MF cases. CD8+ MF was frequent (23%) and CD7 was the most frequently lost antigen in both MF (45%) and CD30LPD (86%), while no significant T-cell antigen loss was observed in BID. CD7 loss was less frequent in folliculotropic MF (p<0.001). PD-1 was variably expressed in MF with no differences with BID. The CD3+/CD7- and PD-1+/CD7- neoplastic lymphocytes were highlighted by the use of chromogenic double staining experiments in MF with a CD7 loss identified with single staining. Multiple pan T-cell antigen losses were mostly seen in CD30LPD with CD2 being the most frequently preserved marker (90%). While PD-1 does not discriminate between MF and BID, CD7 is frequently lost in MF infiltrates as well as other pan-T-cell antigens in CD30LPD, which can be used as routine markers for diagnosis. We recommend the use of CD7 in addition to CD3, CD4 and CD8 as a minimal immunohistochemical panel for MF assessment, and the use of double stainings for CD3 and CD7 in difficult cases.

摘要

蕈样肉芽肿(MF)和原发性皮肤 CD30 阳性 T 细胞淋巴增生性疾病(CD30LPD)是最常见的原发性皮肤 T 细胞淋巴瘤。我们的目的是研究大量 MF 和 CD30LPD 病例中的泛 T 细胞抗原和 PD-1 表达,特别关注抗原缺失作为一种诊断工具。我们回顾性分析了 3 年内 153 例患者的 160 例连续样本,包括 104 例 MF 和 49 例 CD30LPD。作为对照,研究了良性炎症性皮肤病(BID,n=19)。对 CD2、CD3、CD4、CD5、CD7、CD8 的表达进行了半定量评估。在 MF 病例亚组中进行了 PD-1 和双染色(CD3+CD7 和 PD-1+CD7)。在 MF 中,CD8+MF 很常见(23%),CD7 是最常缺失的抗原(MF 中为 45%,CD30LPD 中为 86%),而 BID 中则没有明显的 T 细胞抗原缺失。滤泡性 MF 中 CD7 缺失的频率较低(p<0.001)。MF 中 PD-1 的表达不同,与 BID 无差异。在 MF 中,使用显色双重染色实验突出显示 CD3+/CD7-和 PD-1+/CD7-肿瘤性淋巴细胞,在单染色中识别出 CD7 缺失。在 CD30LPD 中,大多数病例存在多种泛 T 细胞抗原缺失,而 CD2 是最常保留的标志物(90%)。虽然 PD-1 不能区分 MF 和 BID,但 CD7 在 MF 浸润物中以及在 CD30LPD 中的其他泛 T 细胞抗原中经常缺失,可作为诊断的常规标志物。我们建议将 CD7 与 CD3、CD4 和 CD8 一起用作 MF 评估的最小免疫组化面板,并在困难病例中使用 CD3 和 CD7 的双重染色。

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