Miglani Ripan K, Murthy Divakar, Bhat Ravi Shanker, Ashok Kumar K V
Department of Surgical Gastroenterology, Bangalore Medical College and Research Institute, Bangalore, India ; 67 B Tagore Nagar, Civil Lines, Ludhiana, Punjab 141001 India.
Indian J Surg. 2012 Aug;74(4):301-4. doi: 10.1007/s12262-011-0394-3. Epub 2012 Jan 21.
Anorectal malformations (ARMs) are one of the most common congenital anomalies dealt by surgeons. The reported incidence of ARMs range between 1:3,300 and 1:5,000 live births. These defects are invariably detected and treated in infancy or early childhood. There is a group of patients among these who have fistulous external opening from the rectum. These may not present in child hood and may continue to live with fecal incontinence till adult hood. One of such anomalies is rectovaginal fistulas which comprises of only 4% of all anomalies. Delayed management in such cases increases surgical and functional complications. Traditionally high and intermediate anorectal anomalies are treated by posterior sagittal anorectoplasty (PSARP). This involves cutting of sphincter muscles in the midline and then placement of rectum in the sphincter complex. The continence results of this operation are less than ideal. Laparoscopically assisted anorectal pull-through (LAARP) has potential advantage of precise placement of the rectum inside the sphincter complex without dividing and weakening the muscles, diminished soft tissue scarring around the rectum leading to improved rectal compliance. Three adult female patients with ARMs were managed through LAARP procedure. It involves dissection around rectum, identification and ligation of fistula tract, creation of neoanus and pull through of rectum into neoanus. Results-Continence was good in all our patients which they regained after 3 to 4 days of surgery. On follow up which ranged from 6 months to 2 years all were passing well formed stools 1-2 times a day and have symmetric anal contraction with strong squeeze on digital rectal examination. Conclusion-LAARP offers an excellent option to the patients of ARM over conventional posterior sagittal anorectal approach because if its theoretical advantages of early recovery and better continence. Long term followup is needed to substantiate these results.
肛门直肠畸形(ARMs)是外科医生处理的最常见先天性畸形之一。报道的ARMs发病率在每3300至5000例活产婴儿中有1例。这些缺陷总是在婴儿期或幼儿期被发现并接受治疗。在这些患者中有一组存在直肠瘘管外口。这些瘘管在儿童期可能不会出现,患者可能会一直存在大便失禁,直到成年。其中一种这样的畸形是直肠阴道瘘,仅占所有畸形的4%。在这种情况下延迟治疗会增加手术和功能并发症。传统上,高位和中位肛门直肠畸形通过后矢状位肛门直肠成形术(PSARP)治疗。这包括在中线切断括约肌,然后将直肠放置在括约肌复合体中。该手术的控便效果并不理想。腹腔镜辅助肛门直肠拖出术(LAARP)具有潜在优势,即能将直肠精确放置在括约肌复合体内,而无需切断和削弱肌肉,减少直肠周围的软组织瘢痕,从而改善直肠顺应性。3例成年女性肛门直肠畸形患者通过LAARP手术进行治疗。该手术包括直肠周围的解剖、瘘管的识别和结扎、新肛门的创建以及将直肠拖入新肛门。结果——我们所有患者的控便情况良好,术后3至4天恢复。随访时间为6个月至2年,所有患者每天排便1至2次,大便成形,直肠指检时肛门收缩对称且有力。结论——由于LAARP具有早期恢复和更好控便的理论优势,与传统后矢状位肛门直肠手术相比,它为肛门直肠畸形患者提供了一个极佳的选择。需要长期随访来证实这些结果。