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黑热病后皮肤利什曼病的病理学:皮肤病变及引流淋巴结的光镜、免疫组织化学和超微结构研究

Pathology of post-kala-azar dermal leishmaniasis: a light microscopical, immunohistochemical, and ultrastructural study of skin lesions and draining lymph nodes.

作者信息

Ismail Ahmed, Gadir A Fattah A, Theander Thor G, Kharazmi Arsalan, El Hassan Ahmed M

机构信息

Department of Clinical Pathology and Immunology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan.

出版信息

J Cutan Pathol. 2006 Dec;33(12):778-87. doi: 10.1111/j.1600-0560.2006.00531.x.

Abstract

BACKGROUND

Whereas the clinical manifestations and treatment of post-kala-azar dermal leishmaniasis (PKDL) have been adequately described before, the pathology received little attention, particularly the African form of PKDL which shows some clinical differences from the disease in India. Therefore, our aim was to characterize the pathology and the immunohistopathology in PKDL lesions and correlate the histopathological findings with the clinical features of the disease.

METHODS

Biopsies of skin lesions were examined for histopathological changes in formalin-fixed tissues and for cell phenotypes and adhesion molecules by immunohistochemistry.

RESULTS

The epidermis showed various changes in different combinations. The dermis was infiltrated by lymphocytes and macrophages, but plasma cells were scanty or absent. The majority of cells were CD3 T cells, with a preponderance of CD4 over CD8 cells. Degenerating basal keratinocytes expressed HLA-DR, ICAM-1 and Leishmania antigen and closely interacted with CD4 T cells. Regional lymph nodes showed hyperplasia of the B- and T-cell zones.

CONCLUSIONS

The inflammatory reaction in PKDL lesions is in response to Leishmania parasites and/or antigen. The majority of cells are CD4 T cells. Degeneration of the basal keratinocytes is probably due to the action of cytotoxic CD4 T cells interacting with leishmania-expressing epidermal cells. Ismail A, Gadir AFA, Theander TG, Kharazmi A, El Hassan AM. Pathology of post-kala-azar dermal leishmaniasis: a light microscopical, immunohistochemical, and ultrastructural study of skin lesions and draining lymph nodes.

摘要

背景

尽管之前已经对黑热病后皮肤利什曼病(PKDL)的临床表现和治疗进行了充分描述,但病理学方面却很少受到关注,尤其是非洲型PKDL,它在临床症状上与印度的该疾病存在一些差异。因此,我们的目的是对PKDL病变的病理学和免疫组织病理学进行特征描述,并将组织病理学发现与该疾病的临床特征相关联。

方法

对皮肤病变活检组织进行检查,观察福尔马林固定组织中的组织病理学变化,并通过免疫组织化学检测细胞表型和黏附分子。

结果

表皮呈现出不同组合的各种变化。真皮有淋巴细胞和巨噬细胞浸润,但浆细胞稀少或缺失。大多数细胞为CD3 T细胞,其中CD4细胞多于CD8细胞。退化的基底角质形成细胞表达HLA-DR、ICAM-1和利什曼原虫抗原,并与CD4 T细胞密切相互作用。区域淋巴结显示B细胞和T细胞区增生。

结论

PKDL病变中的炎症反应是对利什曼原虫寄生虫和/或抗原的反应。大多数细胞是CD4 T细胞。基底角质形成细胞的退化可能是由于细胞毒性CD4 T细胞与表达利什曼原虫的表皮细胞相互作用的结果。伊斯梅尔·A、加迪尔·AFA、安德 TG、哈拉兹米·A、埃尔·哈桑·AM。黑热病后皮肤利什曼病的病理学:皮肤病变和引流淋巴结的光镜、免疫组织化学及超微结构研究。

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