Haneke E
Z Hautkr. 1984 Jul 15;59(14):951-61.
In a 53-year-old man with Sézary's syndrome, histology showed unique epithelial islands originating from the sweat glands, epithelioid granulomas with giant cells in lymph nodes, and abundant foam cells in the papillary layer as well as perivascularly in the upper dermis and lymph nodes. Severe cholestatic granulomatous hepatitis and hyperlipoproteinemia caused further aggravation of the disease.
在一名患有塞扎里综合征的53岁男性患者中,组织学检查显示有源自汗腺的独特上皮岛、淋巴结中伴有巨细胞的上皮样肉芽肿、乳头层以及真皮上层和淋巴结血管周围有大量泡沫细胞。严重的胆汁淤积性肉芽肿性肝炎和高脂蛋白血症导致病情进一步加重。