中华皮肤科杂志 ›› 2021, Vol. 54 ›› Issue (10): 884-887.doi: 10.35541/cjd.20200682

• 研究报道 • 上一篇    下一篇

二期梅毒41例免疫组化特征分析

巩慧子    王涛    郑和义    李军   

  1. 中国医学科学院、北京协和医学院北京协和医院皮肤科  100730
  • 收稿日期:2020-07-06 修回日期:2021-01-21 发布日期:2021-09-28
  • 通讯作者: 李军 E-mail:lijun35@hotmail.com
  • 基金资助:
    北京市科技计划课题(Z191100006619011);首都卫生发展科研专项项目(2020-2-4016)

Analysis of immunohistochemical characteristics of 41 cases of secondary syphilis

Gong Huizi, Wang Tao, Zheng Heyi, Li Jun   

  1. Department of Dermatology and Venereology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
  • Received:2020-07-06 Revised:2021-01-21 Published:2021-09-28
  • Contact: Li Jun E-mail:lijun35@hotmail.com
  • Supported by:
    Beijing Municipal Science and Technology Planning Project (Z191100006619011); Capital′s Funds for Health Improvement and Research (2020-2-4016)

摘要: 【摘要】 目的 探索梅毒螺旋体在二期梅毒皮疹中的分布特点及其与组织病理的相关性。方法 选取2008年1月至2018年12月在北京协和医院皮肤性病科通过组织病理检查,并根据临床表现和血清学检查确诊的二期梅毒患者41例,分析皮损组织切片的免疫组化结果,并以此为分组依据,分析不同组间临床及组织病理特点的差异。对连续数据使用t检验或Kruskal-Wallis检验评估两组间差异;对分类数据使用卡方或Fisher精确检验来评估组间差异。结果 免疫组化检查显示,42份二期梅毒皮损切片中,68.3%存在梅毒螺旋体,主要分布于表皮下部及真皮浅中层。以斑疹为主的二期梅毒疹的梅毒螺旋体阳性率[80%(16/20)]较以丘疹为主的二期梅毒疹[50%(11/22)]高(P < 0.05)。在10种病理特征中,免疫组化阳性组较阴性组更常表现出皮突延长(P < 0.05)、基底细胞液化变性(P < 0.05)、角质层中性粒细胞浸润(P < 0.05)、苔藓样浸润模式(P < 0.05)、点状角质形成细胞坏死(P < 0.05)。免疫组化显示有较多数量梅毒螺旋体的切片表现出更多病理特征(H = 17.914,P < 0.001)。梅毒螺旋体免疫组化染色显示有大量(8份)、中量(14份)及少量(5份)梅毒螺旋体的切片分别平均有8种、7种及6种梅毒特异性组织病理特征;15份梅毒螺旋体免疫组化阴性的组织切片平均只有4种病理特征。 结论 免疫组化可以显示梅毒螺旋体在二期梅毒皮疹中的分布,梅毒螺旋体含量较多的组织切片显示更多的梅毒特异性病理特征。

关键词: 梅毒, 诊断, 苍白密螺旋体, 免疫组织化学, 病理过程

Abstract: 【Abstract】 Objective To investigate distribution characteristics of Treponema pallidum (Tp) in secondary syphilis lesions, and to analyze its correlation with histopathological findings. Methods Totally, 41 patients were collected from Department of Dermatology and Venereology, Peking Union Medical College Hospital from January 2008 to December 2018, who were confirmedly diagnosed with secondary syphilis according to clinical manifestations and serological examinations, and had undergone histopathological examinations. Immunohistochemical results of skin tissue sections were analyzed, and differences in clinical and histopathological characteristics were analyzed between immunohistochemically Tp-positive and Tp-negative sections. Continuous data were compared by using t test or Kruskal-Wallis test, and categorical data were compared by using Chi-square test or Fisher′s exact test. Results Immunohistochemical examination showed that Tp was detected in 68.3% of the 42 secondary syphilis tissue sections, and Tp was mainly distributed in the lower epidermis and superficial and middle dermis. The positive rate of Tp was significantly higher in secondary syphilis lesions mainly manifesting as maculae (80% [16/20]) than in those mainly manifesting as papules (50% [11/22], P < 0.05). Among 10 pathological characteristics, extended rete ridges, basal cell liquefaction degeneration, neutrophil infiltration in the stratum corneum, lichenoid pattern of infiltration and punctate keratinocyte necrosis were observed more frequently in immunohistochemically Tp-positive sections than in Tp-negative sections(all P < 0.05). Immunohistochemical study revealed that tissue sections with a larger number of Tp showed more pathological features (H = 17.914, P < 0.001). Immunohistochemical staining showed that there were 8, 7 and 6 syphilis-specific histopathological characteristics on average in 8 tissue sections with a larger number of Tp, 14 with a medium number of Tp and 5 with a small number of Tp, respectively; while only 4 syphilis-specific histopathological characteristics were observed on average in 15 immunohistochemically Tp-negative tissue sections. Conclusion Immunohistochemical staining could show the distribution of Tp in secondary syphilis lesions, and it seems that tissue sections with a larger number of Tp present with more syphilis-specific histopathological characteristics.

Key words: Syphilis, Diagnosis, Treponema pallidum, Immunohistochemistry, Pathologic processes