Tang Yunman, Huang Jin, Chen Shaoji, Huang Lugang, Wang Minghe
School of Preclinical and Forensic Medicine, Sichuan University, Chengdu Sichuan 610041, P R China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2006 Mar;20(3):217-9.
To investigate the anatomical features of congenital chordee without hypospadias in children and to discuss the diagnosis and treatment.
From August 1984 to December 2004, 94 children with chordee without hypospadias treated in the West China Hospital of Sichuan University were classified and analyzed for anatomical alterations. Their ages ranged from 18 months to 13 years (mean 6. 9 years). Ninety-four patients were divided into four groups. With intraoperation artificial erection, the patients with penis straightened after degloving were classified as type I patients (skin-tethering), those with penis straightened after fibrotic tissue in Buck's fascia released as type II patients (dysgenetic fascia), those with normal urethra and orthoplasty failed after degloving and removing fibrotic tissue as type III patients (corporal disproportion), and those with dysgenetic urethra tethering the corpora cavernosa as type lV patients (short urethra).
In type I (n = 31, 32.9%) patients, the ventral skin and dartos fascia were contracted while Buck's fascia and the urethra was normal, in some (7 cases) scrotal skin extended to the ventral portion of penis (webbed penis). In type II (n = 45, 47.9%), contracture of Buck's fascia was evident and the thickening fibrotic tissue constituted the chief obstacle to orthoplasty, though in some skin was shortened. In type III (n = 6), the dorsal and ventral sides of the corpora cavernosa were disproportionated, and the morphologically normal urethra tightly adhered to the ventral aspect of corpora cavernosa. In some cases ventral skin and fascia were contracted, but orthoplasty could not be achieved through releasing these layers. In type IV (n = 12, 12.8%), the distal urethra was paper-thin and lacking corpus spongiosum, or dense fibrotic bands were found to be deep to the urethra. The urethra tethered the corpora cavernosa and formed a bow-to-string relation. The overlying skin and fascia were contracted in varying degrees while none had significance in straightening the penis. After operation, the length of penis increased to 6.9 cm from 5.2 cm on average and the chordee was corrected to 1.6 degrees from 42.6 degrees before operation on average. The patients were followed up 1 months to 15 years. The results were satisfactory. Chordee remained in 2 cases, fistula and urethral stricture occurred in 2 cases respectively, fistula in association with urethral stricture and diverticulum in 1 case; the operation was given again and the results was satisfactory.
Patients with chordee without hypospadias may be divided into four types depending on which layer of the ventral penis constitutes the chief contribution to chordee. A systematic approach with repeated artificial erection tests is needed in determining the classification and surgical correction.
探讨小儿先天性阴茎下弯(无尿道下裂)的解剖学特点,并讨论其诊断与治疗。
1984年8月至2004年12月,四川大学华西医院收治的94例先天性阴茎下弯(无尿道下裂)患儿,对其解剖学改变进行分类分析。年龄18个月至13岁(平均6.9岁)。94例患儿分为4组。术中通过人工勃起,脱套后阴茎伸直者为Ⅰ型(皮肤束缚型);Buck筋膜内纤维化组织松解后阴茎伸直者为Ⅱ型(发育异常筋膜型);脱套及切除纤维化组织后尿道正常但阴茎矫形失败者为Ⅲ型(海绵体不均衡型);尿道发育异常束缚海绵体者为Ⅳ型(短尿道型)。
Ⅰ型(n = 31,32.9%)患儿,阴茎腹侧皮肤及肉膜收缩,Buck筋膜及尿道正常,部分(7例)阴囊皮肤延伸至阴茎腹侧(蹼状阴茎)。Ⅱ型(n = 45,47.9%),Buck筋膜挛缩明显,增厚的纤维化组织是阴茎矫形的主要障碍,部分患儿皮肤也有缩短。Ⅲ型(n = 6),海绵体背腹侧不均衡,形态正常的尿道紧密附着于海绵体腹侧。部分病例腹侧皮肤及筋膜收缩,但松解这些层次无法实现阴茎矫形。Ⅳ型(n = 12,12.8%),尿道远端菲薄,缺乏海绵体,或尿道深部有致密纤维化带。尿道束缚海绵体,形成弓弦样关系。覆盖其上的皮肤及筋膜不同程度收缩,对阴茎伸直均无明显作用。术后阴茎长度平均从5.2 cm增加至6.9 cm,阴茎下弯平均从术前42.6°矫正至1.6°。随访1个月至15年。结果满意。2例仍有阴茎下弯,2例分别出现尿瘘及尿道狭窄,1例尿瘘合并尿道狭窄及憩室;再次手术,效果满意。
先天性阴茎下弯(无尿道下裂)患儿可根据阴茎腹侧哪一层结构是导致阴茎下弯的主要因素分为4型。确定分型及手术矫正需要采用系统方法并反复进行人工勃起试验。