Yamaguchi T, Fukuda T, Uetani M, Hayashi K, Kurosaki N, Maeda H, Matsumoto T, Miyake H
Department of Radiology, Nagasaki University School of Medicine, 1-7-1 Sakamoto, Nagasaki 852, Japan.
Pediatr Radiol. 1996;26(5):312-4. doi: 10.1007/BF01395704.
We report the case of a patient with Beckwith-Wiedemann syndrome (BWS) who developed renal cell carcinoma (RCC). At birth, this patient presented with macroglossia, diastasis recti, mild gigantism, hepatomegaly and hypoglycemia, and the diagnosis of BWS was made. At 22 months, an intrapelvic rhabdomyosarcoma was detected and resected. At 37 months, computed tomography (CT) demonstrated a small mass with high attenuation in the right kidney, which was surgically confirmed to be RCC.
我们报告了一例患有贝克威思-维德曼综合征（BWS）并发展为肾细胞癌（RCC）的患者。该患者出生时表现为巨舌、腹直肌分离、轻度巨人症、肝肿大和低血糖，遂诊断为BWS。22个月时，检测到盆腔内横纹肌肉瘤并进行了切除。37个月时，计算机断层扫描（CT）显示右肾有一个高衰减的小肿块，手术证实为肾细胞癌。
