Vasudev Rao T, Alkindi Salam, Pathare A V
Department of Pathology, College of Medicine and Health Sciences, Sultan Qaboos University, Alkhoud, Muscat, Oman.
Pathol Res Pract. 2007;203(6):479-84. doi: 10.1016/j.prp.2006.12.006. Epub 2007 Apr 5.
We report a case of a multicentric plasma cell (PC) variant of Castleman's disease (CD) in association with interfollicular type of classic Hodgkin's disease (HD), both diseases identified in the same lymph node. The histologic features of CD were the classic ones, with hyperplastic and atrophic follicles, some with prominent mantle zones, hyalinzed vessels, and a very rich polyclonal proliferation of PCs in the interfollicular region. The presence of LCA-negative, but CD30- and CD15-positive typical and atypical Reed-Sternberg (RS) cells in the interfollicular region confirmed the presence of HD. In addition, many of the RS cells stained positive for EBV. CD35- and CD21-positive follicular dendritic cell (FDC) hyperplasia was a striking feature, a finding that has not been well documented in the PC variant of CD.
我们报告了一例多中心性Castleman病(CD)的浆细胞(PC)变异型,与经典霍奇金淋巴瘤(HD)的滤泡间型相关,这两种疾病在同一淋巴结中被发现。CD的组织学特征是典型的,有增生性和萎缩性滤泡,一些有明显的套区、玻璃样变血管,以及滤泡间区域非常丰富的多克隆性PC增殖。滤泡间区域存在LCA阴性但CD30和CD15阳性的典型和非典型里德-斯腾伯格(RS)细胞,证实了HD的存在。此外,许多RS细胞EBV染色呈阳性。CD35和CD21阳性的滤泡树突状细胞(FDC)增生是一个显著特征,这一发现在CD的PC变异型中尚未得到充分记录。