雙陰莖:罕見病例報告及文獻回顧
陳鴻毅、吳俊德、黃賢祥、林政鋒、陳文祥、林承家
基隆長庚醫院 外科部 泌尿科
Diphallia: A rare case report and literature review
Hung-Yi Chen, Chun-Te Wu, Shian-Shiang Huang, Cheng-Feng Lin, Wen-Hsiang Chen, Cheng-chia Lin
Divisions of Urology, Department of Surgery, Chang Gung Memorial Hospital, Keelung
Case report:
Diphallia or penile duplication is an extremely rare congenital anomaly that occurs in 1 of 5 million births. The appearance varies from a small accessory penis to complete duplication and it is associated with other urogenital, gastrointestinal, cardiac and musculoskeletal congenital malformations. Here, we reported a 68 year-old man with incidental finding of diphallia with a review of the articles pertaining to this anomaly. On examination, there was penile duplication with two incompletely separate phalluses, unequal in size without other associated anomaly (hypospadias, bifid scrotum) who was hospitalized for massive pleural effusion study.