Slater D N, Rooney N, Harrington C, Tucker W F, Beck S, Walker A E, Grundman M J
Histopathology. 1984 Nov;8(6):927-36. doi: 10.1111/j.1365-2559.1984.tb02411.x.
Two elderly female patients are described with generalized histiocytosis X (Letterer-Siwe disease). In each case, a definitive diagnosis was not established until ultrastructural and immunoperoxidase investigations had been performed. The histopathological findings in skin biopsies from each patient were similar. Light microscopy demonstrated a bandlike epidermotrophic cellular infiltrate which included large atypical cells (histiocytosis X cells). Electron microscopy showed that these cells contained Birbeck granules. Monoclonal antibody studies demonstrated the presence of T6, T4 and HLA-DR surface antigens. Lysozyme and alpha-I-antitrypsin were absent from the cells. The associated cellular infiltrate included T4 and T8 positive lymphocytes. It is possible that more cases of generalized histiocytosis X in adults will be identified with the increasing use of specialized histopathological techniques and that the disease is more common than currently believed.
本文描述了两名患有全身性组织细胞增多症X(勒-雪病)的老年女性患者。在每例患者中,直到进行了超微结构和免疫过氧化物酶检查才确诊。两名患者皮肤活检的组织病理学结果相似。光镜检查显示带状表皮嗜细胞浸润,其中包括大的非典型细胞(组织细胞增多症X细胞)。电镜检查显示这些细胞含有Birbeck颗粒。单克隆抗体研究表明存在T6、T4和HLA-DR表面抗原。细胞中未检测到溶菌酶和α-1抗胰蛋白酶。相关的细胞浸润包括T4和T8阳性淋巴细胞。随着专业组织病理学技术的日益广泛应用,可能会发现更多成人全身性组织细胞增多症X病例,且该病可能比目前认为的更为常见。