Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai 400012, India.
J Pediatr Surg. 2010 Jul;45(7):1538-41. doi: 10.1016/j.jpedsurg.2010.03.012.
A newborn boy was brought to us, 2 hours after birth, with a mucosal-lined left hemiperineal lesion associated with classical bladder exstrophy and an anterolaterally displaced anus. Perineal anatomy was restored by excising the mucosa lined lesion. The bladder closure for classical bladder exstrophy was done at the same time. Histologically, gastric, respiratory, and small intestinal epithelia were present in the mucosa. A rectal duplication cyst that had ruptured in utero through the hemiperineum could explain the anomaly. The association of classical bladder exstrophy with ruptured rectal duplication cyst has never previously been described in the literature.
一个出生后 2 小时的男婴被带来，左侧会阴有黏膜衬里的部分性半器官裂，伴有典型的膀胱外翻和肛门前外侧移位。通过切除黏膜衬里病变来修复会阴解剖结构。同时进行经典膀胱外翻的膀胱关闭术。组织学上，黏膜中存在胃、呼吸和小肠上皮。一个直肠重复囊肿在子宫内破裂通过半器官裂进入会阴，可以解释这种异常。经典膀胱外翻与破裂的直肠重复囊肿的关联在文献中从未有过描述。
