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首页> 外文期刊>Journal of plastic, reconstructive & aesthetic surgery: JPRAS >Surgical approach to the congenital megaprepuce.
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Surgical approach to the congenital megaprepuce.

机译:先天性大包皮的手术方法。

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摘要

The megaprepuce (MP) is a very rare malformation of unknown aetiology, with anatomical findings similar to those observed in the congenital buried penis (BP). The aspect of this entity and the symptoms are rather typical: the penis is totally buried and before micturition an evident pubic and scrotal swelling denounces the urine collection in an abnormal preputial cavity surrounding the entire shaft. Early surgery is recommended, in order to deal with functional and cosmetic aspects. The very diminutive phallus is the most important cause of family anxiety. The authors present six infants, aged 5, 12, 13, 18, 20 and 43 months, operated upon for MP. The surgical approach consisted in the complete exteriorization of the shaft with section of the penile ligament, the restoring of the pubo-penile and peno-scrotal angles and the tailoring of the cutaneous cylinder. No intra- or postoperative complications were observed. Late functional and cosmetic results were judged satisfactory by both parents and surgeons. The surgical approach to BP is not simply transferable to the correction of MP. The cosmetic arrangement of the shaft skin is the more difficult step of the MP correction in order to avoid postoperative complications and an unsatisfied cosmetic appearance.
机译:megaprepuce(MP)是一种非常罕见的病因不明的畸形,其解剖学发现与先天性阴茎勃起(BP)相似。该实体的外观和症状相当典型:阴茎完全被掩埋,排尿前明显的耻骨和阴囊肿胀使尿液聚集在整个轴周围的异常包膜腔中。建议尽早进行手术,以处理功能和美容方面的问题。极小的阴茎是家庭焦虑的最重要原因。作者介绍了六个接受MP手术的婴儿,分别为5、12、13、18、20和43个月。手术方法包括用阴茎韧带的一部分将轴完全外化,耻骨-阴茎和阴囊阴囊角的恢复以及皮肤圆柱体的剪裁。没有观察到术中或术后并发症。父母和外科医生均认为后期的功能和美容效果令人满意。 BP的手术方法不能简单地转移到MP的校正上。为了避免术后并发症和不满意的美容外观,杆身皮肤的美容布置是MP矫正中比较困难的步骤。

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