Abstract

Introduction: Anorectal malformations (ARMs) are congenital conditions with varying clinical presentations. The approximate incidence is 1:2,500 to 1:5,000 live births. Diagnosis and treatment are usually performed in childhood; therefore, ARMs are relatively rare in adults. However, some cases can go unnoticed in underdeveloped countries due to health care barriers and errors. Globally, few cases of ARMs have been reported in adulthood, so the literature is limited. Medical debate continues about the best approach and follow-up of the patient. The objective of this case is to describe the main gastroenterological points for consideration. Case Description/Methods: A 54-year-old female patient product of a vaginal birth delivered outside of medical facilities by unqualified personnel. Throughout the patient's childhood, she consulted different clinics and public health services for infections secondary to the discharge of feces through the vagina. In 2021, she was seen at a family medicine clinic of the national university in Guatemala for osteoarthritis. In her medical history, she mentioned the ARM condition and was referred to a proctologist who diagnosed an Imperforate Anus (Figure A) and a Rectovestibular Fistula, even though she had successfully delivered 3 infants by c-section. An MRI was ordered to rule out any other associated malformations prior to surgery. Subsequently, a 2-stage surgery under spinal anesthetic block was performed: First, a loop colostomy and Peña Posterior Sagittal Anorectoplasty were done (Figure B, C), with a thinning of the elevator and anus muscles diagnosed. Three months later a colostomy closure was performed. The patient has been followed monthly for 6 months with satisfactory results with anal dilatation reserved, if necessary, but the functionality of the neo-anus has, to date, been adequate. Discussion: The main points for consideration are a) age should not be a contraindication for corrective surgery; b) the functionality of the sphincter complex must be determined in each patient; c) due to the congenital etiology of the imperforate anus, as well as physiological and the anatomical changes, there has been no developed hemorrhoidal vascular network; d) the main anticipated complication is cicatricial stenosis of the neo-anus secondary to the surgical intervention, so programmed anal dilations should be considered if needed. Given the rarity of ARMs in adults, further manometric research of the physiology of the anal complex is required to establish functionality parameters.Figure 1.: Anorectoplasty Process: (a) Imperforate anus, (b) Anorectoplasty with reconstruction of the rectovaginal septum, (c) Anoplasty.

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