Kawai K, Harada T, Matsukuma H, Nakashita Y
Acta Pathol Jpn. 1978 Sep;28(5):787-96. doi: 10.1111/j.1440-1827.1978.tb00917.x.
A case of Letterer-Siwe disease of a 1-year-2-month-old boy, which clinicopathologically satisfied 7 out of the 8 characteristics of the disease by Siwe's criteria, excluding pathologic changes in the bone is reported. The vacuolated histiocytes appeared in the proliferating reticuloendothelial cells in this case; the cells were positive by general fat reaction; the fats consisted of cholesterol fats, phospholipids and neutral lipid. Electron microscopy showed the occurrence of lipid droplets with cholesterol crystals and atypical form of Langerhans cell granule. Granulomatous changes were found in the lymph nodes and spleen, and this case was also similar in part to chronic granulomatous disease; however, celoid and lipofuscin pigments were negative in the proliferating cells. Cytomegalic inclusion disease as a complication was found in the lungs and intestine, and bilirubin stones in the liver.
报告了一例1岁2个月男童的勒-雪病,根据西韦标准,该病例临床病理表现符合该病8项特征中的7项,不包括骨骼的病理变化。本例增殖的网状内皮细胞中出现空泡化组织细胞;这些细胞对一般脂肪反应呈阳性;脂肪由胆固醇脂、磷脂和中性脂质组成。电子显微镜显示存在含胆固醇晶体的脂滴和非典型形式的朗格汉斯细胞颗粒。在淋巴结和脾脏中发现肉芽肿性改变,该病例在部分方面也类似于慢性肉芽肿病;然而,增殖细胞中的类胆色素和脂褐素呈阴性。在肺和肠道中发现巨细胞包涵体病作为并发症,肝脏中发现胆红素结石。