Background: The aim of this study was to evaluate the efficacy of a combination of flaps for the reconstruction of presacral defects following abdominoperineal resections: a paramedian vertically oriented caudally based lotus petal flap for presacral defects combined with a horizontal V-Y advancement flap for closure of the superficial donor site defect.
Methods: A retrospective study was conducted on patients with a residual defect following an abdominoperineal resection between 2010 and 2017 in the Noordwest Ziekenhuisgroep. The primary endpoint was complications related to the reconstruction.
Results: Twelve patients were included, all reconstructions healed well. Three patients had a grade I or II complication (Clavien Dindo classification).
Conclusions: Use of a petal flap and V-Y advancement flap for reconstruction of presacral defects was found to be safe and simple, and should, therefore, be considered in the management of such problems.
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http://dx.doi.org/10.1007/s10151-020-02204-x | DOI Listing |
Ann Med Surg (Lond)
December 2024
General Surgery Department "B", La Rabta Hospital, The Faculty of Medicine, The University of Tunis El Manar, Tunis, Tunisia.
Introduction And Importance: Deep-located glomangiomas are rarely reported. Because of their scarcity, treatment strategy is hard to establish. Herein, the authors report the first case to our knowledge of pre-sacral glomangioma.
View Article and Find Full Text PDFJ Surg Case Rep
November 2024
Surgery Department, Darwish Nazal Governmental Hospital, Ministry of Health, Darwish Nazal Hospital St., Qalqileyah 00970, Palestine.
Afr J Paediatr Surg
October 2024
Department of Pediatric Surgery, AIIMS, Jammu, Jammu and Kashmir, India.
Afr J Paediatr Surg
July 2024
Department of Paediatric Surgery, SVP Institute of Medical Sciences and Research, NHL Municipal Medical College, Ahmedabad, Gujarat, India.
Tailgut cysts are rare congenital abnormalities that develop due to failure of embryologic tailgut to involute. This generally manifests as a presacral, retrorectal and multicystic mass. It has a high propensity in female patients including paediatric age group.
View Article and Find Full Text PDFJ Cancer Res Ther
April 2024
Department of Pediatric Surgery, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
Currarino syndrome (CS) is a rare congenital syndrome characterized by a triad of anorectal malformation, sacral deformity, and presacral mass. In about 50% of cases, it is caused by HLXB9 gene mutation in chromosome 7q36. A 13-month-male child presented with presacral discharging sinus with a history of surgery for anorectal malformation and perineal fistula at the time of birth.
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