Kim C Y, Cho B K, Kim I O, Hwang Y S, Wang K C
Division of Pediatric Neurosurgery, Seoul National University Children's Hospital, South Korea.
Pediatr Neurosurg. 1997 Feb;26(2):103-6. doi: 10.1159/000121171.
Cerebral sparganosis in childhood is very rare. Until 1996, 2 cases in children up to 15 years of age had been described. We report a case of cerebral sparganosis in a 6-year-old girl who presented with seizures. Sequential brain magnetic resonance imaging scans spaced over 4 months showed a lesion which migrated from the right parieto-occipital region to the right occipital region. The enzyme-linked immunosorbent assay for antisparganum antibody was positive. She most likely contracted sparganosis from worm-infested spring-water. A live worm with surrounding granulomatous tissue was removed, and the enzyme-linked immunosorbent assay for antisparganum antibody converted to negative 12 months following surgery. In areas of endemic sparganosis, the possibility of cerebral sparganosis should be considered, even in a child, if the patient shows a migrating granulomatous lesion.
儿童脑裂头蚴病非常罕见。截至1996年,已报道过2例15岁以下儿童的病例。我们报告1例6岁患癫痫的女童脑裂头蚴病病例。间隔4个月的连续脑部磁共振成像扫描显示,一个病灶从右顶枕区移至右枕区。抗裂头蚴抗体的酶联免疫吸附测定呈阳性。她很可能是因饮用受蠕虫感染的泉水而感染裂头蚴病。一条带有周围肉芽肿组织的活虫被切除,术后12个月抗裂头蚴抗体的酶联免疫吸附测定转为阴性。在裂头蚴病流行地区,如果患者出现游走性肉芽肿病变,即使是儿童,也应考虑脑裂头蚴病的可能性。