New Jersey Medical School, Newark, NJ, USA.
RWJ Saint Barnabas Medical Center, West Orange, NJ, USA; New York-Presbyterian Weill Cornell Hospital, New York, USA.
J Pediatr Urol. 2018 Oct;14(5):422.e1-422.e5. doi: 10.1016/j.jpurol.2018.04.028. Epub 2018 May 30.
The glans penis may show a deep groove (surgically favorable), or may appear flat with an absent sulcus (unfavorable). Glans dehiscence following hypospadias repair, especially after multiple surgeries, frequently results in a scarred, obliterated, or absent urethral plate. The glans penis appears to be flat and grooveless. This study reported on the outcome of a two-stage salvage repair for glans dehiscence in 49 consecutive patients.
Retrospective chart review was performed for all patients who underwent repair for glans dehiscence following hypospadias repair.
Between January 2009 and April 2015, 49 children aged 16 months to 18 years presented with glans dehiscence following hypospadias repair. The prior number of operations ranged from one to six. Eleven children had urethral fistulas, and seven had chordee. In the first stage, the flat glans was incised deeply to visualize, but spare, the corpora. Thereafter, a free graft of oral mucosa harvested either from the lower lip or cheek, or the residual preputial skin, was sutured to the glans cleft. The grafts were fenestrated, quilted in the midline, and a tie-over dressing was applied. Any fistula or chordee was repaired during the first stage. The neo-plate was tubularized 6-12 months later, and urine drainage with a catheter was maintained for 10-14 days. In 11 patients, skin flaps appeared dusky, and nitroglycerine ointment 2% was applied for 24 h to enhance the blood supply of the tissues. Subsequently, six of these children received nine or ten 90-min hyperbaric oxygen therapy sessions. Following the first stage, two patients developed hypertrophy of the mucosal grafts, and one skin graft contracted. These three patients underwent revision using a second buccal mucosal graft harvested from the cheek. One recurrent fistula was closed during the second stage. Following the second stage two patients developed a urethral fistula, and the distal sutures broke down in one patient, resulting in an over-sized meatus. None developed meatal stenosis or glans dehiscence.
Graft initial take and subsequent behavior were unpredictable, but the two stage approach optimized the process of take and healing. Glans dehiscence was repaired safely and successfully by developing a deep groove, with creation of a new urethral plate followed by tubularization in two stages.
龟头可能会出现深沟(手术有利),也可能看起来平坦且没有沟(不利)。尿道下裂修复后,尤其是多次手术后,龟头常会出现裂开,导致疤痕、消失或缺失尿道板。龟头看起来平坦且没有沟。本研究报告了 49 例连续患者行两阶段修复术治疗龟头裂开的结果。
对所有接受尿道下裂修复术后发生龟头裂开的患者进行了修复回顾性图表分析。
2009 年 1 月至 2015 年 4 月,49 名 16 个月至 18 岁的儿童因尿道下裂修复后出现龟头裂开而就诊。之前的手术次数从 1 次到 6 次不等。11 名患儿有尿道瘘,7 名有阴茎弯曲。在第一阶段,深切开平坦的龟头以显露,但要保留阴茎体。然后,将从下唇或脸颊上切取的口腔黏膜游离移植物,或残留的包皮皮瓣,缝合到龟头裂处。移植物被开窗,中线缝合,并应用缝线固定。在第一阶段修复任何瘘管或阴茎弯曲。6-12 个月后,将新尿道板进行管状化,并用导管引流尿液 10-14 天。在 11 名患者中,皮瓣看起来呈暗紫色,应用 2%硝酸甘油软膏 24 小时以增强组织的血液供应。随后,其中 6 名患儿接受了 9 或 10 次 90 分钟高压氧治疗。第一阶段后,两名患儿的黏膜移植物肥大,一名患儿的皮肤移植物收缩。这三名患儿接受了从脸颊上切取的第二块颊黏膜移植物的修复。第二阶段时,闭合了一个复发性瘘管。第二阶段后,两名患儿出现尿道瘘,一名患儿的远端缝线断裂,导致尿道口过大。无患者发生尿道狭窄或龟头裂开。
移植物的初始存活和后续表现不可预测,但两阶段方法优化了存活和愈合过程。通过在两阶段创建新的尿道板并进行管状化,安全有效地修复了龟头裂开。