Oak S, Rao S, Karmarkar S, Kulkarni B, Kalgutkar A, Malde A, Naik L
Department of Pediatric Surgery, L.T.M.G. Hospital, Sion, Bombay 400 022, India.
Pediatr Surg Int. 1997 Jul;12(5-6):424-5. doi: 10.1007/BF01076957.
A 2-year-old boy who presented with a cystic gallbladder mass was found histologically to have metachromatic leukodystrophy. Diffuse hyperplasia of the gallbladder mucosa, multiple tendrillar fronds extending into the lumen, extensive papillomatosis, and the presence of large numbers of macrophages bearing metachromatic material confirmed the diagnosis. The child developed progressive degeneration of the central nervous system, refractory bronchopneumonia, and generalized muscular atrophy. A computed tomographic scan of the brain demonstrated hypodense areas of white matter suggestive of demyelination. This report describes the rare association of gallbladder papillomatosis with a storage disorder and reviews the relevant literature.
一名2岁男孩因胆囊囊性肿物就诊,组织学检查发现患有异染性脑白质营养不良。胆囊黏膜弥漫性增生、多个伸向管腔的丝状叶、广泛的乳头瘤病以及大量含有异染物质的巨噬细胞的存在证实了诊断。该患儿出现中枢神经系统进行性退化、难治性支气管肺炎和全身肌肉萎缩。脑部计算机断层扫描显示白质低密度区提示脱髓鞘。本报告描述了胆囊乳头瘤病与一种贮积病的罕见关联,并回顾了相关文献。