Unusual Presentation of a Rectovestibular Fistula as Gastrointestinal Hemorrhage in a Postmenopausal Woman [PDF]
Case Reports in Obstetrics and Gynecology, 2014 Background. Anorectal malformations (ARMs) are extremely rare and are usually identified neonatally. It is unusual for these cases to present in the postmenopausal period.
Olga Grechukhina +4 more
doaj +6 more sources
Neonatal Sweet’s syndrome associated with rectovestibular fistula with normal anus [PDF]
Pediatric Reports, 2015 Sweet’s syndrome, characterized by fever and a painful erythematous rash with a dermal neutrophilic infiltrate, develops primarily due to paraneoplastic phenomena in adults. Sweet’s syndrome is very rare in neonates.
Jun Shinozuka +7 more
doaj +7 more sources
Effect of megarectum on postoperative defecation of female patients with congenital rectovestibular fistula or rectoperineal fistula [PDF]
Frontiers in Pediatrics, 2023 BackgroundTo assess the effect of megarectum on postoperative defecation of female patients with congenital rectovestibular fistula or rectoperineal fistula.MethodsFrom March 2013 to February 2021, 74 female patients with congenital rectovestibular ...
Chunxiang Liu +9 more
doaj +5 more sources
Anorectal Malformation with Rectovestibular Fistula and Vaginal Agenesis: Usage of Rectovestibular Fistula as a Neovagina Followed by PSARP with Preservation of the Anal Sphincter [PDF]
European Journal of Pediatric Surgery Reports, 2021 Anorectal malformation with rectovestibular fistula associated with vaginal agenesis is rare. We report on a child in whom this combination was diagnosed at the age of 1 year. After creation of a divided descending colostomy, we chose to leave the rectum-
Antonio Dessanti +3 more
doaj +5 more sources
Congenital rectovestibular fistula associated with rectal atresia: A rare occurrence
Journal of Indian Association of Pediatric Surgeons, 2013 We report a rare variety of anorectal malformation, rectal atresia associated with rectovestibular fistula. The case was successfully treated by posterior sagittal repair.
Rizwan Ahmad Khan, Rajendra Singh Chana
doaj +4 more sources
Imperforate anus with a rectovestibular fistula and pseudotail: a case report [PDF]
Journal of Medical Case Reports, 2010 Introduction Human tails and pseudotails are rare sacrococcygeal lesions that are associated with a wide variety of anomalies and syndromes. Anorectal malformations are also relatively uncommon congenital defects that often occur in conjunction with ...
Jackson Gretchen P +2 more
doaj +5 more sources
One-stage vs. three-stage repair in anorectal malformation with rectovestibular fistula
African Journal of Paediatric Surgery, 2016 Background: Anorectal malformations (ARMs) disease is one of the congenital anomalies with an incidence of about 1 in 5000 neonate births, and treatment requires surgical intervention.
Omid Amanollahi, Saman Ketabchian
doaj +4 more sources
Tubular Colonic Duplication Presenting as Rectovestibular Fistula. [PDF]
Pediatr Gastroenterol Hepatol Nutr, 2015 Complete colonic duplication is a very rare congenital anomaly that may have different presentations according to its location and size. Complete colonic duplication can occur in about 15% of all gastrointestinal duplications. Double termination of tubular colonic duplication in the perineum is even more uncommon.
Karkera PJ +5 more
europepmc +4 more sources
Evaluation of a modified one-stage technique for repair of third-degree perineal laceration and rectovestibular fistula with rectal pull-back technique in 12 mares: a retrospective case series [PDF]
BMC Veterinary ResearchAim This study was carried out to evaluate a rectal pull-back one-stage technique, which is a modification of the one-stage Goetz technique, for treating third-degree perineal laceration or rectovestibular fistula.
Ahmed Sharshar +3 more
doaj +2 more sources
A Female Infant with Rectovestibular Fistula and Imperforate Hymen.
J Indian Assoc Pediatr Surg, 2023 ABSTRACT In a female neonate with anorectal malformation (ARM), the diagnosis is usually simple. But when there are two openings in the introitus and absent anal opening at the normal site, the scenario poses a diagnostic challenge.
Khedkar K +3 more
europepmc +3 more sources