Govender D, Chetty R
Department of Anatomical Pathology, Faculty of Medicine, University of Natal, Durban, South Africa.
J Clin Pathol. 1997 Jan;50(1):79-81. doi: 10.1136/jcp.50.1.79.
A lesion of the chest wall in a 34 year old woman, which had a combination of histological and immunophenotypic features of inflammatory pseudotumor and Rosai-Dorfman disease of soft tissue, is described. There was considerable overlap in the pathogenesis, histology and immunophenotype of these two lesions. The similarities between these two lesions suggest that there is a temporal sequence and a histological continuum with early histiocyte-rich and late fibroblast- and myofibroblast-rich lesions. Alternatively, the morphological and immunophenotypic features could be because of aberrant cytokine expression in an inflammatory pseudotumour, resulting in transformation of histiocytes to resemble those seen in Rosai-Dorfman disease.
描述了一名34岁女性胸壁的病变,其具有炎性假瘤和软组织Rosai-Dorfman病的组织学和免疫表型特征。这两种病变在发病机制、组织学和免疫表型方面有相当多的重叠。这两种病变之间的相似性表明存在一个时间顺序和组织学连续体,早期以富含组织细胞的病变为主,晚期以富含成纤维细胞和肌成纤维细胞的病变为主。或者,形态学和免疫表型特征可能是由于炎性假瘤中细胞因子表达异常,导致组织细胞转化,类似于Rosai-Dorfman病中所见的细胞。