摘要
病例一,女,6岁,因“出生后发现下腹壁缺损伴外生殖器异常、无肛”入院。患儿出生后发现无肛门,大小便自会阴部同一开口排出,伴腹壁缺损及黏膜样组织外翻,当地医院考虑畸形较严重,几年来一直未治疗,入院前出现排便困难,及腹壁外翻组织有少许渗液流出而转至本院,体格检查:腹软,略胀,未见正常脐部,耻骨联合、腹直肌分离,下腹部腹壁见局部组织发育异常,两处皮肤缺损,伴鲜红色黏膜样组织外翻,大小分别约2.5 cm ×3 cm、3 cm ×2 cm,组织表面见淡黄色渗液,会阴部无正常尿道、阴道和肛门,大阴唇处见皮赘一枚,上翻皮赘见一直径约1 cm开口,大小便均自此开口排出(图1 a、b)。
出处
《临床小儿外科杂志》
CAS
2014年第4期363-364,366,共3页
Journal of Clinical Pediatric Surgery
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