Dynamic defecography in the diagnosis of paediatric rectal prolapse and related disorders

Background and aim Paediatric rectal prolapse (RP) is rarely a diagnostic problem and resolves often spontaneously. We studied whether the assessment of recurrent RP (RP), postoperative relapsed RP (RRP) or anorectal discomfort without RP (ARD) benefits from dynamic defecography (DD) and describe DD...

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Veröffentlicht in:Pediatric surgery international 2012-08, Vol.28 (8), p.815-820
Hauptverfasser: Koivusalo, A. I., Pakarinen, M. P., Rintala, R. I., Seuri, R.
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Sprache:eng
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Zusammenfassung:Background and aim Paediatric rectal prolapse (RP) is rarely a diagnostic problem and resolves often spontaneously. We studied whether the assessment of recurrent RP (RP), postoperative relapsed RP (RRP) or anorectal discomfort without RP (ARD) benefits from dynamic defecography (DD) and describe DD findings in relation with outcome. Patients and methods Fifteen patients (7 males), median age of 10 (range 3.7–15) years, underwent 19 DD with a synchronic small bowel contrast study. Indications for DD were RP ( n  = 11), RD ( n  = 3) and RRP ( n  = 1). Three patients had solitary rectal ulcer and one juvenile rectal polyps ( n  = 1). Three patients underwent a total of four postoperative DD because of suspected relapse. Results In 11 patients with a clinically diagnosed prolapse DD displayed a simple prolapse ( n  = 3), prolapse with enterocele ( n  = 1), prolapse with small bowel interposition ( n  = 1), rectal intussusception with anterior rectocele ( n  = 1) and rectal intussusception ( n  = 1) and no pathology ( n  = 4) (37 %). In four patients with ARD DD displayed rectal prolapse originating from sigmoid intussusception ( n  = 1), enterocele ( n  = 1) and anterior rectocele ( n  = 1) and no pathology in one. Median follow-up was 8.1(range 3.0–44) months. Ten patients underwent surgery. Three patients with RP underwent simple laparoscopic rectopexy, five with RP or RD with enterocele or anterior rectocele had rectopexy with anterior peritoneoplasty and two (RP n  = 1, RRP n  = 1) with sigmoid intussusception had sigmoid resection with rectopexy. Two symptomatic patients (RP, negative DD) are scheduled for rectopexy. Three patients PPRP ( n  = 2) RD ( n  = 1) had spontaneous cure. Postoperative DD confirmed relapsed RP in one patient. Conclusion In patients, RP and associated disorders’ DD can disclose significant pathology (enterocele, rectocele or sigmoid intussusception) and thereby guide surgical treatment, and should be included in the pre-treatment assessment.
ISSN:0179-0358
1437-9813
DOI:10.1007/s00383-012-3125-3