Snover D C, Frizzera G, Spector B D, Perry G S, Kersey J H
Hum Pathol. 1981 Sep;12(9):821-31. doi: 10.1016/s0046-8177(81)80085-8.
Seventeen lymph nodes and 13 spleens from 15 patients with the Wiskott-Aldrich syndrome were examined histologically. The material included both biopsy and autopsy specimens. Consistent findings included depletion of small lymphocytes from T cell areas (all cases), prominence of the reticulum cell stroma (all cases), the presence of atypical plasma cells with and without plasmacytosis (16 lymph nodes and 11 spleens), and extramedullary hematopoiesis (13 lymph nodes and 9 spleens). Less frequent features noted were tissue eosinophilia, hemophagocytosis, focal fibrosis, and progressive depletion of germinal centers. One case with a unique abundance of transformed lymphocytes is described.
对15例维斯科特-奥尔德里奇综合征患者的17个淋巴结和13个脾脏进行了组织学检查。材料包括活检和尸检标本。一致的发现包括T细胞区小淋巴细胞减少(所有病例)、网状细胞基质突出(所有病例)、有或无浆细胞增多的非典型浆细胞的存在(16个淋巴结和11个脾脏)以及髓外造血(13个淋巴结和9个脾脏)。较少见的特征包括组织嗜酸性粒细胞增多、噬血细胞现象、局灶性纤维化和生发中心逐渐减少。描述了1例具有独特大量转化淋巴细胞的病例。