摘要
报道7例血管淋巴组织增生伴嗜酸细胞浸润和Kimura病。结果显示:两者为同一种疾病的不同阶段。前者以小淋巴和小扭核细胞浸润,为多克隆性;后者出现中扭核细胞,为单克隆性。复发病例则随病情的发展从小扭核细胞向中扭核细胞过渡,亦为单克隆性。结果提示,本病有从良性向恶性发展的趋势,上皮样和组织细胞样血管增生是本病特征之一。
The clinical, pathologic and immunohistochemical features of 7 cases of angiolymphoid hyperplasia with eosinophilia (ALHE) and kimura's disease are dis-cribed, indicating that they are different stages of the same disease. Morphologically, there are small round and irregular lymphoid cells infiltrating that are polyclon-al in ALHE, and middle cerebriform lym-
phoid cells that are monoclonal in Kimura's disease. A recurrent case varies in its spectrum ,of cytologic expression. Therefor, this lesion may be transformed from benign into malignant. Epithelioid or/and histiocy-toid blood vessels is another characteristic feature.
出处
《临床与实验病理学杂志》
CAS
CSCD
北大核心
1994年第4期299-301,T006,共4页
Chinese Journal of Clinical and Experimental Pathology
