Nakazawa Shigeaki, Yoneda Suguru, Takezawa Kentaro, Tanigawa Go, Fujita Kazutoshi, Okumi Masayoshi, Hosomi Masahiro, Fukuhara Shinichiro, Fushimi Hiroaki, Yamaguchi Seiji
The Department of Urology, Osaka Geneal Medical Center.
Hinyokika Kiyo. 2012 Apr;58(4):215-8.
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease with multiple neurofibroma and café-au-lait spots. We report a case of plexiform neurofibroma of the bladder associated with NF1. A 34-year-old female was referred to our hospital for thickness of the bladder wall. Multiple café-au-lait spots and neurofibroma was found on her skin,and she was diagnosed with neurofibromatosis type 1. Ultrasound examination demonstrated bladder wall thickening,and cystoscopy revealed an irregular and erythematous mucosa. Transurethral biopsy of the bladder wall was performed. Histopathological diagnosis was plexiform neurofibroma of the bladder.
1型神经纤维瘤病(NF1)是一种常染色体显性疾病,表现为多发性神经纤维瘤和咖啡斑。我们报告1例与NF1相关的膀胱丛状神经纤维瘤病例。一名34岁女性因膀胱壁增厚被转诊至我院。在其皮肤上发现多处咖啡斑和神经纤维瘤,她被诊断为1型神经纤维瘤病。超声检查显示膀胱壁增厚,膀胱镜检查发现黏膜不规则且呈红斑状。对膀胱壁进行了经尿道活检。组织病理学诊断为膀胱丛状神经纤维瘤。