先天性双侧唇裂伴男性假两性畸形1例报告  

Congenital bilateral cleft lip with male artificial bisexual deformity :one case report

作　　者：焦建军[1] 张学强[1] 靳书滨[1] 陈振东[1] 

机构地区：[1]河北省邯郸市中心医院口腔科,河北邯郸056001

出　　处：《中国口腔颌面外科杂志》2004年第3期217-218,共2页China Journal of Oral and Maxillofacial Surgery

摘　　要：本文报告1例先天性双侧唇裂伴发男性假两性畸形患者。该患者左侧上睑下垂;双侧上唇自唇红缘向上至双侧鼻底全部裂开,双侧鼻翼扁平,中唇短小、前翘、左偏;前颌突与双侧上颌突完全分离;外阴部在自然状态下极似女性,可见"大阴唇",仅见小块阴囊皮肤,未触及睾丸,拨开"大阴唇"可露出短小的阴茎。B超可探及2个隐蔽的睾丸。该患者经行双唇裂修复术后痊愈出院。The paper described a patient who suffered from a congenital bilateral cleft lip with artificial bisexual deformity. The patient's left upper eyelid was ptosis. The bilateral upper lips were completely separated from vermillion border to the floor of nose. The bilateral wings of nose were flat. The middle lip was short and small and warpeded to front and left. Bilateral globular process and maxillary process were completely not united. The vulva looked just as the female's in natural condition; 'The greater lip of pudendum' could be looked, only a piece of skin of scrotum could be seen and the testicles could not be touched. Pushing apart 'the greater lip of pudendum', a small penis could be found. Two enorchia could be detected by B type ultrasonography. The patient had been discharged after repair of the bilateral cleft lip.

关 键 词：先天性畸形 双侧唇裂 男性似两性畸形 

分 类 号：R782.22[医药卫生—口腔医学]