Rossete-Cervantes Héctor Enrique, Villegas-Muñoz Alvaro
Facultad de Medicina, Universidad Autónoma de Tlaxcala, Tlaxcala, México.
Rev Med Inst Mex Seguro Soc. 2016 May-Jun;54(3):401-3.
The diphallia is a rare anatomic abnormality that occurs in 1 of 5 million births. The etiology is unknown and its appearance varies from a small accessory penis to complete duplication and it is associated with other urogenital, gastrointestinal, cardiac and musculoskeletal congenital malformations. Several classifications have been designed according to the anatomical characteristics and their study is complemented by ultrasound and magnetic resonance imaging. Treatment should be early and individualized in order to achieve a satisfactory aesthetic and functional result.
We report the incidental finding of diphallia without other anatomical malformations associated in an adult of 83 years old who was hospitalized and died of severe head trauma.
The case presented is relevant for the infrequency of this alteration, the absence of other anatomical malformations associated and the age at which it was detected.
双阴茎是一种罕见的解剖学异常,在每500万例出生中出现1例。病因不明,其外观从小的附属阴茎到完全重复不等,并且与其他泌尿生殖系统、胃肠道、心脏和肌肉骨骼先天性畸形相关。已经根据解剖学特征设计了几种分类方法,超声和磁共振成像对其研究起到补充作用。治疗应尽早且个体化,以获得满意的美学和功能效果。
我们报告了一例83岁成年男性因严重头部创伤住院并死亡,偶然发现双阴茎且无其他相关解剖学畸形的病例。
该病例因这种改变罕见、无其他相关解剖学畸形以及发现时的年龄而具有相关性。