Abstract

Isolated torsion of the Fallopian tube, without ovarian torsion, is a rare cause of lower abdominal pain. We report our experience with 4 recent cases, along with data from a 20-year review of the pediatric literature. The records of 4 cases encountered during a 3-year period were reviewed. A literature review was completed by searching Medline, Medline in Process, Embase, Current Contents, and BIOSIS from 1990 to 2010. All 4 patients were diagnosed on laparoscopy. Laparoscopic salpingectomy was performed in 3 cases and laparoscopic detorsion in 1. All three resected specimens revealed hemorrhage and gangrene of the salpinx, with an associated cyst in one. The pediatric literature review, including our report, revealed 33 case reports and case series with 45 patients. Fifty-six percent of cases represented primary torsion, and 44% were secondary to underlying tubal pathology. Thirty percent of girls were premenarchal. The mean age at presentation and symptom duration were 13.2±2.1 years and 5.8±12.5 days, respectively. Fever and leukocytosis were present in 27% and 63%, respectively. Ultrasound, computed tomography scan, and magnetic resonance imaging showed a sensitivity of 22% (8/36), 14% (1/7), and 40% (2/5), respectively. A correct preoperative diagnosis was considered in only 13%. Eighty-eight percent of cases were treated by salpingectomy, and 12% were treated by tubal detorsion. Long-term outcomes of detorsion were not reported. Isolated salpingeal torsion in girls is rarely diagnosed preoperatively, regardless of imaging technique. Laparoscopy is the intervention of choice for definitive diagnosis and management. Salpingectomy is the most frequent treatment. Detorsion without resection may be considered for selected cases, but the long-term outcomes of this approach are unknown.

Highlights

  • Cleft lip and/or palate (CL/P) are an embryonic syndrome which consists of cleft lip, cleft lip and palate, and cleft palate, and which accounts for 65% of all the congenital malformations of the head and the neck [1]

  • Data on orofacial clefts are sparsely available in respect of Africa, and this is even truer in Burkina Faso where there are no published studies on CL/P dedicated to the pediatric subpopulation

  • In Burkina Faso, care of orofacial clefts is difficult, and to alleviate the governmental inadequacies, local, European and Canadian Non-Governmental Organizations (NGO) organize humanitarian campaigns to bring the specialized care of surgery to the patients

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Summary

Introduction

Cleft lip and/or palate (CL/P) are an embryonic syndrome which consists of cleft lip, cleft lip and palate, and cleft palate, and which accounts for 65% of all the congenital malformations of the head and the neck [1]. Data on orofacial clefts are sparsely available in respect of Africa, and this is even truer in Burkina Faso where there are no published studies on CL/P dedicated to the pediatric subpopulation. It is a recent study which revealed that CL/P constituted 70.6% of all congenital malformations of the face and the neck in Ouagadougou [4]. This study is aimed to describe the epidemiological, clinical aspects and management of CL/P among children seen within the framework of humanitarian missions of pediatric plastic surgery in Ouagadougou in Burkina Faso. Conclusions: Epidemiological and clinical characteristics of cleft lip and/or palate

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