Nishimura K, Sugao H, Sato K, Okuyama A, Sonoda T
Department of Urology, Osaka University Hospital, Japan.
Urol Int. 1991;46(1):109-11. doi: 10.1159/000281794.
We report an unusual case of clitoral hypertrophy due to neurofibromatosis of the external genitalia. Because of no definite skin signs or other nervous or osseous symptoms such as are commonly found in neurofibromatosis, the patient was at first suspected of being a case of hermaphroditism. Finally, the disorder was properly diagnosed after laparotomy followed by clitorectomy. This patient seems to be the 12th case of clitoral neurofibroma reported in the English literature.
我们报告了一例因外生殖器神经纤维瘤病导致阴蒂肥大的罕见病例。由于没有神经纤维瘤病常见的明确皮肤体征或其他神经或骨骼症状，该患者最初被怀疑为两性畸形病例。最终，在剖腹手术及阴蒂切除术后，该疾病得到了正确诊断。该患者似乎是英文文献中报道的第12例阴蒂神经纤维瘤病例。
