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Journal of Pediatric Surgery
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    Article Type

    • Rapid Communication33
    • Research Article4

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    Author

    • Chang, Yu-Tang2
    • Holcomb, George W III2
    • Jesudason, Edwin C2
    • Lee, Jui-Ying2
    • Nadler, Evan P2
    • Olguner, Mustafa2
    • Solari, Valeria2
    • Stephenson, Jacob2
    • Aarabi, Shahram1
    • Akbıyık, Fatih1
    • Akgür, Feza M1
    • Akkoyun, Ibrahim1
    • Altunkeser, Aysegul1
    • Aquino, Antonio1
    • Arbuckle, Susan1
    • Ateş, Oǵuz1
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    • Bracco, Gian Luca1
    • Bradley, Tabetha1
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    • Journal of Pediatric Surgery37

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    • Child3
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    • Adolescent2
    • Children2
    • Cyst2
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    • Ovary2
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    • Rapid Communication

      Surgical treatment of inspissated bile syndrome using a 2-stage pure laparoscopic approach: A case report

      Journal of Pediatric Surgery
      Vol. 47Issue 12e47–e50Published in issue: December, 2012
      • Justus Lieber
      • Femke E. Piersma
      • Ekkehard Sturm
      • Jürgen F. Schäfer
      • Jörg Fuchs
      • Philipp O. Szavay
      Cited in Scopus: 4
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        We describe a 99-day old girl with inspissated bile syndrome (IBS) unresponsive to treatment with oral ursodeoxycholic acid. We performed a pure laparoscopic 2-stage procedure, consisting of cholecystostomy and insertion of an indwelling balloon catheter for local ursodeoxycholic acid flushing for 13 consecutive days. Subsequently, the cholecystostomy was removed, preserving the gallbladder using the same laparoscopical approach when bilirubin values returned to normal and bile duct obstruction was no longer detectable radiologically.
        Surgical treatment of inspissated bile syndrome using a 2-stage pure laparoscopic approach: A case report
      • Research Article

        Laparoscopic management of colonic complications in Ehlers-Danlos syndrome type IV

        Journal of Pediatric Surgery
        Vol. 47Issue 11e1–e3Published in issue: November, 2012
        • Gillian Duthie
        • Michael Singh
        • Ingo Jester
        Cited in Scopus: 8
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          Ehlers-Danlos syndrome type IV, also known as the vascular type, is the most severe form of the disease. It may cause spontaneous bowel perforation and rupture of major arteries. The treatment of bowel perforation in this population remains controversial because they are at risk for major wound complications owing to poor healing. We report the first use of laparoscopy in children with Ehlers-Danlos syndrome.
        • Research Article

          Early diverting colostomy for perianal sepsis in children with acute leukemia

          Journal of Pediatric Surgery
          Vol. 47Issue 10e23–e27Published in issue: October, 2012
          • Alessio Pini Prato
          • Elio Castagnola
          • Concetta Micalizzi
          • Carlo Dufour
          • Stefano Avanzini
          • Luca Pio
          • and others
          Cited in Scopus: 9
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            Perineal sepsis is a life-threatening complication of acute leukemia. Although conservative management (antibiotics, incision, and drainage, alone or in combination) is considered the criterion standard, it provides an outcome that is not fully satisfactory, with an overall mortality of roughly 30%. This report presents a case series of 4 children who underwent early defunctioning colostomy for the treatment of perineal sepsis during leukemia. This management proved to be successful and allowed prompt reestablishment of chemotherapy, thus improving overall results.
            Early diverting colostomy for perianal sepsis in children with acute leukemia
          • Rapid Communication

            Successful laparoscopic removal of mesenteric and omental cysts in toddlers: 3 cases with a literature review

            Journal of Pediatric Surgery
            Vol. 47Issue 8e5–e8Published in issue: August, 2012
            • Arzu Pampal
            • Aydin Yagmurlu
            Cited in Scopus: 17
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              Mesenteric and omental cysts are rare benign intraabdominal anomalies with uncertain etiologies. Surgical removal is the preferred treatment owing to complications related to cyst enlargement. A 1-year-old boy with an intrauterine diagnosis of a cystic mass adjacent to his stomach and liver, a 3-year-old girl, and a 3-year-old boy with an incidental diagnosis of intraabdominal cysts were scheduled for laparoscopic surgery. The mass of the 1-year-old boy was a multiloculated cyst originating from the lesser omentum, the incidental mass in the girl was a multiseptated cyst located in the jejunoileal mesentery, and the incidental mass of the 3-year-old boy was a uniloculated cyst originating from the ileal mesentery.
              Successful laparoscopic removal of mesenteric and omental cysts in toddlers: 3 cases with a literature review
            • Rapid Communication

              Laparoscopic excision of a giant splenic vascular tumor

              Journal of Pediatric Surgery
              Vol. 47Issue 7e21–e23Published in issue: July, 2012
              • E. Marty Knott
              • Patricia A. Valusek
              • Shawn D. St. Peter
              Cited in Scopus: 0
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                The splenic vascular tumor referred to as a hemangioma is rare and typically presents as a small asymptomatic lesion. We report a case of a giant splenic cyst in a 13-year-old boy with abdominal distension. He underwent laparoscopic excision of the splenic cyst without complication. Pathology revealed a vascular tumor. At 15 months of follow-up, he continued to be asymptomatic, and abdominal ultrasound showed no recurrence of his disease. Laparoscopic excision of giant splenic cysts is a viable option in children, allowing for preservation of normal splenic tissue.
                Laparoscopic excision of a giant splenic vascular tumor
              • Rapid Communication

                Early laparoscopic repair for blunt duodenal perforation in an adolescent

                Journal of Pediatric Surgery
                Vol. 47Issue 5e11–e14Published in issue: May, 2012
                • Chein-Lin Huang
                • Jui-Ying Lee
                • Yu-Tang Chang
                Cited in Scopus: 5
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                  Duodenal perforation secondary to blunt abdominal trauma in children is rare and usually associated with delays in diagnosis and surgical intervention. The authors encountered such a case in a 12-year-old boy owing to his falling over the handlebar of a bicycle. Imaging examination showed that there was a perforation over the fourth portion of the duodenum without concomitant injuries. Using a 5-port transperitoneal laparoscopic technique, primary closure of the perforation was successfully performed at 6 hours after the impact.
                  Early laparoscopic repair for blunt duodenal perforation in an adolescent
                • Rapid Communication

                  Laparoscopic-assisted perineal pull-through vaginoplasty

                  Journal of Pediatric Surgery
                  Vol. 47Issue 4e13–e15Published in issue: April, 2012
                  • Ilhan Ciftci
                  Cited in Scopus: 9
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                    Hematometrocolpos is the result of vaginal obstruction and can become an emergency in the pubertal period. The treatment of imperforate hymen is well defined, but the treatment of vaginal atresia is more complex. We report a case of hematometrocolpos secondary to distal vaginal atresia that was operated on in the pubertal period. The patient had isolated distal atresia without persistence of the urogenital sinus. A combined abdominal laparoscopic and perineal approach and a posterior vaginoplasty were carried out.
                    Laparoscopic-assisted perineal pull-through vaginoplasty
                  • Rapid Communication

                    Laparoscopic ureteroureterostomy in children with a duplex collecting system plus obstructed ureteral ectopia

                    Journal of Pediatric Surgery
                    Vol. 47Issue 4e27–e30Published in issue: April, 2012
                    • Mustafa Olguner
                    • Feza M. Akgür
                    • Mehmet Atilla Türkmen
                    • Serdar Şiyve
                    • Gulce Hakgüder
                    • Oğuz Ateş
                    Cited in Scopus: 10
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                      One of the complex upper urinary tract anomalies is a duplicated collecting system. In cases with a functioning upper moiety, ureteroureterostomy (UU) is the preferred operation to redirect the urine to the normal collecting system. Although open UU is a well-described operation, experience with laparoscopic repair pediatric patients is scarce. We describe the successful application of laparoscopic UU in 2 children and suggest that laparoscopic UU for the duplicated collecting system is a promising minimally invasive procedure.
                      Laparoscopic ureteroureterostomy in children with a duplex collecting system plus obstructed ureteral ectopia
                    • Rapid Communication

                      Trichobezoar causing pancreatitis: first reported case of Rapunzel syndrome in a boy in North America

                      Journal of Pediatric Surgery
                      Vol. 47Issue 3e17–e19Published in issue: March, 2012
                      • Jonathan E. Kohler
                      • Michael Millie
                      • Elizabeth Neuger
                      Cited in Scopus: 14
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                        Trichobezoar is a mass of hair retained in the stomach, usually associated with trichotillomania. Large trichobezoars may extend into the small bowel and cause small bowel obstruction or pancreatic dysfunction, a condition known as Rapunzel syndrome. Here we report the first North American case of Rapunzel syndrome in a male patient.
                        Trichobezoar causing pancreatitis: first reported case of Rapunzel syndrome in a boy in North America
                      • Rapid Communication

                        Noningested intraperitoneal foreign body causing chronic abdominal pain: a role for laparoscopy in the diagnosis

                        Journal of Pediatric Surgery
                        Vol. 47Issue 2e15–e17Published in issue: February, 2012
                        • Shahram Aarabi
                        • Jacob Stephenson
                        • Dennis L. Christie
                        • Patrick J. Javid
                        Cited in Scopus: 6
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                          In this article, we present an unusual case of a young boy who presented with abdominal pain and was found to have a sewing needle that had migrated through the abdominal wall into the peritoneal space. After imaging and endoscopy, the needle was extracted laparoscopically without any evidence of intra-abdominal organ injury and with a good long-term outcome for the child. There are no other such reported cases in the literature. This case highlights the subtleties in management of intra-abdominal foreign bodies in children including rare causes such noningested foreign bodies.
                          Noningested intraperitoneal foreign body causing chronic abdominal pain: a role for laparoscopy in the diagnosis
                        • Rapid Communication

                          Laparoscopic cystectomy for splenic hydatid cyst: a case report

                          Journal of Pediatric Surgery
                          Vol. 46Issue 11e1–e3Published in issue: November, 2011
                          • Ibrahim Akkoyun
                          • Fatih Akbıyık
                          • Aysegul Altunkeser
                          Cited in Scopus: 0
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                            Even in countries where it is considered endemic, splenic hydatid cyst is a very rare disease in childhood. Partial or total splenectomy has generally been the treatment of choice for this condition. This is the first report of laparoscopic cystectomy as treatment of isolated splenic hydatid cyst in childhood. A 10-year-old girl with isolated splenic hydatid cyst was successfully treated by laparoscopic cystectomy and splenic preservation. The authors have demonstrated that laparoscopic cystectomy for an isolated splenic hydatid cyst is technically feasible, safe, and is associated with a shorter hospital stay and good cosmetic appearance.
                            Laparoscopic cystectomy for splenic hydatid cyst: a case report
                          • Rapid Communication

                            Pneumatosis intestinalis after laparoscopic appendectomy: case report and review of the literature

                            Journal of Pediatric Surgery
                            Vol. 46Issue 11e21–e24Published in issue: November, 2011
                            • Chris Vendryes
                            • Catherine J. Hunter
                            • Susan R. Harlan
                            • Henri R. Ford
                            • James Stein
                            • James R. Pierce
                            Cited in Scopus: 7
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                              Pneumatosis intestinalis (PI) is the presence of intraluminal gas within the wall of the intestine. As a marker for bowel injury owing to mucosal injury, PI may herald a severe underlying disease process in patients without a significant medical history. In other cases, PI is a benign process, and expectant management is appropriate. Here, we present the first reported case of pneumatosis associated with postoperative abscess after appendectomy and its successful management. Then, we describe the pathophysiology of pneumatosis and review the literature regarding its origin and management.
                              Pneumatosis intestinalis after laparoscopic appendectomy: case report and review of the literature
                            • Rapid Communication

                              Enhancing safety of laparoscopic vascular control for neonatal sacrococcygeal teratoma

                              Journal of Pediatric Surgery
                              Vol. 46Issue 5e5–e7Published in issue: May, 2011
                              • Valeria Solari
                              • Wajid Jawaid
                              • Edwin C. Jesudason
                              Cited in Scopus: 11
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                                Life-threatening bleeding is a hazard of major tumor excision in children. However, fatalities from inadvertent arterial ligation should not be overlooked. Sacrococcygeal teratoma is the commonest neonatal tumor. Laparotomy to ligate the median sacral artery has been used to preempt potentially fatal resectional bleeding. Use of laparoscopy to achieve the same is an evolving technique, with only 7 neonatal cases described. As such, the Idea, Development, Exploration, Assessment, Long-term study (IDEAL) guidelines on surgical innovation recommend case reports addressing proof of concept, technical factors and safety tips.
                                Enhancing safety of laparoscopic vascular control for neonatal sacrococcygeal teratoma
                              • Rapid Communication

                                Laparoscopic repair of traumatic abdominal wall hernia from handlebar injury

                                Journal of Pediatric Surgery
                                Vol. 46Issue 5e9–e12Published in issue: May, 2011
                                • Erin E. Rowell
                                • Anthony C. Chin
                                Cited in Scopus: 18
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                                  A 14-year-old boy was seen at an outside hospital after falling over the handlebar of his bicycle and was discharged home. He was subsequently seen in our emergency department with complaints of persistent abdominal pain. A computed tomography scan of the abdomen revealed disruption of the muscles of the upper right abdominal wall containing the hepatic flexure of the colon, with a small amount of intraperitoneal free fluid noted. The patient underwent laparoscopic exploration using 3 ports (2-5 mm and 1-12 mm) and 2 separate stab incisions.
                                  Laparoscopic repair of traumatic abdominal wall hernia from handlebar injury
                                • Rapid Communication

                                  Dangerous deliveries: lessons learned during retroperitoneal specimen retrieval

                                  Journal of Pediatric Surgery
                                  Vol. 46Issue 4e13–e15Published in issue: April, 2011
                                  • M. Upadhyaya
                                  • L.S. Sundararajan
                                  • M.N. Woodward
                                  Cited in Scopus: 4
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                                    Laparoscopy is now a standard technique in pediatric surgery and urology. Unique complications have been reported during port/instrument insertion and dissection, often relating to issues of visibility or working space. Complications during specimen retrieval are currently unreported. We describe our experience of 2 serious complications occurring during attempted retrieval of a specimen through a port site at the end of the laparoscopic procedure.
                                  • Rapid Communication

                                    Bilateral hydrosalpinx with asynchronous tubal torsion: an exceptional finding in a premenarcheal girl

                                    Journal of Pediatric Surgery
                                    Vol. 46Issue 4e27–e29Published in issue: April, 2011
                                    • Mario Lima
                                    • Michele Libri
                                    • Antonio Aquino
                                    • Dalia Gobbi
                                    Cited in Scopus: 14
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                                      Bilateral hydrosalpinx with asynchronous tubal torsion is an extraordinary event in young girls. This report describes the problems associated with misdiagnosis, therapeutic approach, and the risk of suboptimal treatment of this rare clinical entity in a 13-year-old girl.
                                      Bilateral hydrosalpinx with asynchronous tubal torsion: an exceptional finding in a premenarcheal girl
                                    • Rapid Communication

                                      Peritoneal metastases after laparoscopic nephron-sparing surgery for localized Wilms tumor

                                      Journal of Pediatric Surgery
                                      Vol. 46Issue 3e19–e21Published in issue: March, 2011
                                      • Chan-Hon Chui
                                      • Anselm Chi-Wai Lee
                                      Cited in Scopus: 40
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                                        A 2-year-old girl was referred for the management of the progression of her localized Wilms tumor. She had undergone laparoscopic nephron-sparing surgery for her right Wilms tumor 3 months earlier. Postoperative chemotherapy was commenced 6 weeks later. Subsequent computer tomographic evaluation 12 weeks postsurgery showed local recurrence and peritoneal tumors. These findings were confirmed at laparotomy. We report the first case of peritoneal tumor dissemination after laparoscopic nephron-sparing surgery for localized Wilms tumor.
                                        Peritoneal metastases after laparoscopic nephron-sparing surgery for localized Wilms tumor
                                      • Rapid Communication

                                        Laparoscopic excision of a retroperitoneal lymphatic malformation in a newborn

                                        Journal of Pediatric Surgery
                                        Vol. 46Issue 2e15–e17Published in issue: February, 2011
                                        • Valeria Solari
                                        • Dhanya Mullassery
                                        • Nick Lansdale
                                        • Edwin C. Jesudason
                                        Cited in Scopus: 5
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                                          Abdominal lymphatic malformations may be challenging to eradicate. Retroperitoneal lesions may more difficult to resect than mesenteric ones; however, the latter may predispose to intestinal volvulus, leading to calls for their prompt excision. Such lesions identified perinatally may pose particular challenges: in one case, respiratory failure caused by abdominal distension required emergency drainage followed by later laparoscopic excision; laparoscopy has also been used promptly to diagnose and resect neonatal mesenteric lymphatic malformations with their inherent volvulus risk.
                                          Laparoscopic excision of a retroperitoneal lymphatic malformation in a newborn
                                        • Rapid Communication

                                          Pediatric median arcuate ligament syndrome: first report of familial pattern and transperitoneal laparoscopic release

                                          Journal of Pediatric Surgery
                                          Vol. 45Issue 12e17–e20Published in issue: December, 2010
                                          • Sameh M. Said
                                          • Abdalla E. Zarroug
                                          • Peter Gloviczki
                                          • Raymond C. Shields
                                          Cited in Scopus: 7
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                                            Median arcuate ligament syndrome (MALS) is a rare disorder resulting from luminal narrowing of the celiac artery by the insertion of the diaphragmatic muscle fibers. Surgical management entails division of the median arcuate ligament with or without celiac artery reconstruction. We are presenting an interesting case of a 16-year-old girl with postprandial abdominal pain and weight loss. Her mother also had MALS treated via open celiotomy with complete median arcuate ligament division and patch angioplasty of the celiac artery owing to persistent stenosis at our institution.
                                            Pediatric median arcuate ligament syndrome: first report of familial pattern and transperitoneal laparoscopic release
                                          • Rapid Communication

                                            A retroperitoneal gastric duplication cyst mimicking a simple exophytic renal cyst in an adolescent

                                            Journal of Pediatric Surgery
                                            Vol. 45Issue 10e5–e8Published in issue: October, 2010
                                            • Pei-Haung Chen
                                            • Jui-Ying Lee
                                            • Sheau-Fang Yang
                                            • Jaw-Yuan Wang
                                            • Jao-Yo Lin
                                            • Yu-Tang Chang
                                            Cited in Scopus: 8
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                                              Gastric duplications are rare anomalies and usually occur along the greater curvature of the stomach. The authors herein describe an uncommon case of a retroperitoneal gastric duplication, which was not found during previous emergency laparotomy for suspected peritonitis at another institution. On subsequent computed tomography scan, the lesion was misinterpreted as a simple exophytic renal cyst. Laparoscopy was undertaken because of unresolved symptoms, and a retroperitoneal duplication cyst was successfully excised.
                                              A retroperitoneal gastric duplication cyst mimicking a simple exophytic renal cyst in an adolescent
                                            • Rapid Communication

                                              Laparoscopic management of neonatal paraesophageal hernia with intrathoracic gastric volvulus

                                              Journal of Pediatric Surgery
                                              Vol. 45Issue 8e21–e23Published in issue: August, 2010
                                              • Tabetha Bradley
                                              • Jacob Stephenson
                                              • George Drugas
                                              • Jeffrey R. Avansino
                                              Cited in Scopus: 11
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                                                Intrathoracic gastric volvulus associated with neonatal paraesophageal hernia is very rare in the newborn period. We report a case of a 3-week-old term infant who presented to the hospital with a history of non-bilious vomiting. Workup for hypertrophic pyloric stenosis eventually revealed the presence of a congenital hiatal hernia and intrathoracic gastric volvulus requiring urgent surgical management. The infant underwent successful laparoscopic repair. We discuss the diagnosis and management of this extremely rare surgical cause of neonatal nonbilious emesis.
                                                Laparoscopic management of neonatal paraesophageal hernia with intrathoracic gastric volvulus
                                              • Rapid Communication

                                                Ectopic nephrogenic rests in children: the clinicosurgical implications

                                                Journal of Pediatric Surgery
                                                Vol. 44Issue 12e13–e16Published in issue: December, 2009
                                                • Andrew Cooke
                                                • Aniruddh V. Deshpande
                                                • Eric R. La Hei
                                                • Stuart Kellie
                                                • Susan Arbuckle
                                                • Genevieve Cummins
                                                Cited in Scopus: 13
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                                                  Ectopic nephrogenic rests (ENR) are rare. The incidental discovery of these lesions in children has particular clinicosurgical implications, especially given the association between ENR and the development of extrarenal Wilms' tumors (ERWT).
                                                  Ectopic nephrogenic rests in children: the clinicosurgical implications
                                                • Rapid Communication

                                                  Intradiaphragmatic extralobar sequestration—a rare pulmonary anomaly

                                                  Journal of Pediatric Surgery
                                                  Vol. 44Issue 12e27–e29Published in issue: December, 2009
                                                  • Andreas H. Meier
                                                  • Kathleen D. Eggli
                                                  • Robert E. Cilley
                                                  Cited in Scopus: 13
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                                                    Extralobar pulmonary sequestrations are most commonly found within the thoracic cavity, but have been described within the abdomen. We present the case of a 16-month-old boy with an intradiaphragmatic pulmonary sequestration and demonstrate a computed tomographic scan finding that might help identify this extremely rare abnormality preoperatively.
                                                    Intradiaphragmatic extralobar sequestration—a rare pulmonary anomaly
                                                  • Rapid Communication

                                                    Laparoscopic total esophagogastric dissociation

                                                    Journal of Pediatric Surgery
                                                    Vol. 44Issue 10e1–e3Published in issue: October, 2009
                                                    • Julia Boubnova
                                                    • Geraldine Hery
                                                    • Fabrice Ughetto
                                                    • Arnaud Charpentier
                                                    • Jean-Michel Guys
                                                    • Pascal de Lagausie
                                                    Cited in Scopus: 14
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                                                      The total esophagogastric dissociation (Bianchi's procedure) is used to control the severe gastroesophageal reflux in patients after failure of the fundoplication techniques. The laparoscopic approach can be usefully performed in patients with impaired respiratory function. We report here 2 patients in whom the total esophagogastric dissociation has been entirely performed by laparoscopy. The laparoscopic examination of the proximal esojejunal anastomosis is made feasible using an intestinal clamp placed to avoid the esophageal retraction up into the posterior mediastinum.
                                                      Laparoscopic total esophagogastric dissociation
                                                    • Rapid Communication

                                                      Seven-liter ovarian cyst in an adolescent treated by minimal access surgery: laparoscopy and open cystectomy

                                                      Journal of Pediatric Surgery
                                                      Vol. 44Issue 6e5–e8Published in issue: June, 2009
                                                      • Maria Elisabetta Coccia
                                                      • Francesca Rizzello
                                                      • Gian Luca Bracco
                                                      • Gianfranco Scarselli
                                                      Cited in Scopus: 14
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                                                        Laparoscopic approaches to giant ovarian cysts, particularly in adolescents, have critical management concerns as follows: risk of malignancy, risk of cyst rupture, and limited working space. A 15-year-old girl presented with a giant (>25 cm) ovarian serous cyst adenoma containing 7 L of fluid. At open laparoscopy, a giant, entirely cystic, smooth mass originating from the right ovary and lying between the symphysis and the xiphoid was observed. After intraabdominal fluid aspiration, open conservative cystectomy was performed, avoiding spillage.
                                                        Seven-liter ovarian cyst in an adolescent treated by minimal access surgery: laparoscopy and open cystectomy
                                                      • Rapid Communication

                                                        Laparoscopic diagnosis and treatment of a phenotypic girl with mosaic 45,XO/46,X,idic(Y) mixed gonadal dysgenesis

                                                        Journal of Pediatric Surgery
                                                        Vol. 44Issue 1e1–e3Published in issue: January, 2009
                                                        • Kentaro Mizuno
                                                        • Yoshiyuki Kojima
                                                        • Satoshi Kurokawa
                                                        • Haruo Mizuno
                                                        • Kenjiro Kohri
                                                        • Yutaro Hayashi
                                                        Cited in Scopus: 8
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                                                          We report our experience with laparoscopic gonadal biopsy and gonadectomy for a girl with a dicentric Y chromosome in mixed gonadal dysgenesis (MGD). A 4-year-old phenotypic girl was referred to our hospital because of slight enlargement of the clitoris. Fluorescence in situ hybridization analysis with Y chromosome-specific probes showed a karyotype with 45,XO/46,X,+idic(Y)(p11.32) and presence of the sex-determining region Y sequence. The pathologic finding by frozen section technique using laparoscopic biopsy specimens during the operation demonstrated a left streak gonad and right testis, and she was diagnosed with MGD.
                                                          Laparoscopic diagnosis and treatment of a phenotypic girl with mosaic 45,XO/46,X,idic(Y) mixed gonadal dysgenesis
                                                        • Rapid Communication

                                                          Pacifier-induced bowel obstruction—not so soothing

                                                          Journal of Pediatric Surgery
                                                          Vol. 43Issue 2e13–e15Published in issue: February, 2008
                                                          • Holly L. Neville
                                                          • Jorge Huaco
                                                          • Michael Vigoda
                                                          • Juan E. Sola
                                                          Cited in Scopus: 4
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                                                            Pacifiers are nearly ubiquitous among children in the United States, and although safety regulations exist, the responsibility to choose and maintain a safe pacifier generally falls on the parents, many of whom are unaware of potential hazards. We report a case of a complete bowel obstruction because of an ingested pacifier nipple and recommend increased awareness among practitioners as well as education of parents.
                                                            Pacifier-induced bowel obstruction—not so soothing
                                                          • Rapid Communication

                                                            A large struma ovarii tumor removed via laparoscopy in a 16-year-old adolescent

                                                            Journal of Pediatric Surgery
                                                            Vol. 42Issue 8e19–e22Published in issue: August, 2007
                                                            • Isaac Ezon
                                                            • Nathan Zilbert
                                                            • Lynne Pinkney
                                                            • Jian-Jun Wei
                                                            • Rajesh Malik
                                                            • Evan P. Nadler
                                                            Cited in Scopus: 17
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                                                              Struma ovarii is rare ovarian tumor that is characterized by the presence of at least 50% thyroid tissue on histologic examination. This usually benign neoplasm is predominantly found in women between the ages of 40 and 60 years and infrequently in the pediatric age group. In the foregoing report, we present an unusual case of a large struma ovarii in a 16-year-old adolescent girl with abdominal pain and increasing abdominal girth. Removal of the mass was achieved via a laparoscopic approach. We conclude that the diagnosis of struma ovarii should be considered in adolescent girls presenting with large cystic ovarian masses and that a laparoscopic approach to management is the treatment of choice.
                                                              A large struma ovarii tumor removed via laparoscopy in a 16-year-old adolescent
                                                            • Rapid Communication

                                                              Robotic repair of congenital duodenal atresia: a case report

                                                              Journal of Pediatric Surgery
                                                              Vol. 42Issue 7e31–e33Published in issue: July, 2007
                                                              • John J. Meehan
                                                              Cited in Scopus: 17
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                                                                Although repair of duodenal atresia has been performed laparoscopically, it can be a difficult procedure using rigid handheld laparoscopic instruments. Only a few pediatric surgeons are performing this operation with a minimally invasive approach. Robotic surgery may help overcome the obstacles presented by the use of traditional rigid laparoscopic instruments. We present the world's first robotic repair of congenital duodenal atresia in a 2.4-kg, 1-day-old newborn. The procedure took less than 3 hours, and the patient had an unremarkable postoperative course.
                                                                Robotic repair of congenital duodenal atresia: a case report
                                                              • Rapid Communication

                                                                Laparoscopic splenopexy and cystectomy for an enlarged wandering spleen and splenic cyst

                                                                Journal of Pediatric Surgery
                                                                Vol. 42Issue 5e23–e27Published in issue: May, 2007
                                                                • Prashant Upadhyaya
                                                                • Shawn D. St. Peter
                                                                • George W. Holcomb III
                                                                Cited in Scopus: 11
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                                                                  Wandering spleen is an uncommon condition, which can present emergently in children. Similarly, nonparasitic splenic cysts are also rarely encountered. In this report, we describe a massive wandering spleen (22 cm in longitudinal dimension) with a pseudocyst (4.6 × 2 cm) in the inferior pole in an asymptomatic 16-year-old adolescent. Only 4 similar cases have been reported in the literature; 2 of them have been in the pediatric age group. These 2 conditions were diagnosed while she was being evaluated for dysmenorrhea, and she was referred for surgical consultation.
                                                                  Laparoscopic splenopexy and cystectomy for an enlarged wandering spleen and splenic cyst
                                                                • Research Article

                                                                  Laparoscopic cystojejunostomy as a treatment option for pancreatic pseudocysts in children—a case report

                                                                  Journal of Pediatric Surgery
                                                                  Vol. 41Issue 12e33–e35Published in issue: December, 2006
                                                                  • Guido Seitz
                                                                  • Steven W. Warmann
                                                                  • Hans-Joachim Kirschner
                                                                  • Hans P. Haber
                                                                  • Juergen W. Schaefer
                                                                  • Joerg Fuchs
                                                                  Cited in Scopus: 15
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                                                                    Pancreatic pseudocysts are a rare entity in children for which many approaches have been described. We report on the case of a 5-year-old boy with a pancreatic pseudocyst after blunt abdominal trauma. The patient's clinical and laboratory examination findings had also revealed an acute pancreatitis. His diagnostic workup included ultrasound examination and magnetic resonance cholangiopancreatography. Two large cysts were found at the tail of the pancreas. No injury of the pancreatic or bile duct was found.
                                                                    Laparoscopic cystojejunostomy as a treatment option for pancreatic pseudocysts in children—a case report
                                                                  • Rapid Communication

                                                                    Laparoscopic excision of a giant ovarian cyst after ultrasound-guided drainage

                                                                    Journal of Pediatric Surgery
                                                                    Vol. 41Issue 10e9–e11Published in issue: October, 2006
                                                                    • Oǵuz Ateş
                                                                    • Erdal Karakaya
                                                                    • Gülce Hakgüder
                                                                    • Mustafa Olguner
                                                                    • Mustafa Seçil
                                                                    • Feza M. Akgür
                                                                    Cited in Scopus: 29
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                                                                      The laparoscopic approach to giant ovarian cysts in pediatric population may be difficult regarding the risk of cyst rupture and limited working space. We herein report a 16-year-old adolescent girl that presented with a giant ovarian cyst. To reduce the limitations of the laparoscopy, we performed laparoscopy after draining the cyst under ultrasonographic guidance. Under local anesthesia, a nephrostomy catheter was placed into the cyst by the Seldinger technique. During laparoscopy, abdominal cavity was explored by the scope and then the nephrostomy catheter was removed.
                                                                      Laparoscopic excision of a giant ovarian cyst after ultrasound-guided drainage
                                                                    • Rapid Communication

                                                                      Laparoscopic neo-os creation in an adolescent with uterus didelphys and obstructed hemivagina

                                                                      Journal of Pediatric Surgery
                                                                      Vol. 41Issue 10e19–e22Published in issue: October, 2006
                                                                      • Danielle Patterson
                                                                      • Claudia Mueller
                                                                      • Naomi Strubel
                                                                      • Rafael Rivera
                                                                      • Howard B. Ginsburg
                                                                      • Evan P. Nadler
                                                                      Cited in Scopus: 12
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                                                                        Uterus didelphys is a rare congenital anomaly with a well-documented association with obstructed hemivagina and ipsilateral renal agenesis. Treatment of this anomaly includes drainage of hematocolopos and excision of the vaginal septum, which has traditionally used a scalpel or scissors, often with hymenotomy. Recently, a less invasive approach using hysteroscopic resection has been reported, allowing improved visualization with preservation of the hymenal ring. In this article, we present an alternative minimally invasive approach using a combination of laparoscopy and vaginoscopy in the case of a 10-year-old girl.
                                                                        Laparoscopic neo-os creation in an adolescent with uterus didelphys and obstructed hemivagina
                                                                      • Case report

                                                                        Total laparoscopic left lateral sectionectomy performed in a child with benign liver mass

                                                                        Journal of Pediatric Surgery
                                                                        Vol. 41Issue 1e25–e28Published in issue: January, 2006
                                                                        • Yoo-Seok Yoon
                                                                        • Ho-Seong Han
                                                                        • Yoo Shin Choi
                                                                        • Sang Il Lee
                                                                        • Jin-Young Jang
                                                                        • Kyung-Suk Suh
                                                                        • and others
                                                                        Cited in Scopus: 37
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                                                                          Despite the increasing number of recent reports on laparoscopic liver resection in adults, there are only rare reports on such a procedure being performed in children. The authors report here on a total laparoscopic left lateral sectionectomy that was performed in a 5-year-old girl who had a cystic tumor of the liver. The operative time was 150 minutes, the estimated blood loss was about 100 mL, and no intraoperative transfusion was required. The patient was discharged on postoperative day 11 without any significant complications.
                                                                          Total laparoscopic left lateral sectionectomy performed in a child with benign liver mass
                                                                        • Rapid Communication

                                                                          Laparoscopic cystogastrostomy for the treatment of pancreatic pseudocysts in children

                                                                          Journal of Pediatric Surgery
                                                                          Vol. 40Issue 11e13–e17Published in issue: November, 2005
                                                                          • Daniel F. Saad
                                                                          • Kenneth W. Gow
                                                                          • Samer Cabbabe
                                                                          • Kurt F. Heiss
                                                                          • Mark L. Wulkan
                                                                          Cited in Scopus: 26
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                                                                            Pancreatic pseudocysts (PPSs) are common sequelae of pancreatitis and pancreatic trauma. The management is based upon the pseudocyst size and presence of symptoms. Those requiring intervention are often drained using several available options. The use of laparoscopic cystogastrostomy for large and recurrent PPSs has been described in adult patients as a less morbid alternative to open drainage procedures. This technique is considered a novel approach in children. We describe 2 children who had PPSs amenable to laparoscopic cystogastrostomy.
                                                                            Laparoscopic cystogastrostomy for the treatment of pancreatic pseudocysts in children
                                                                          • Rapid Communication

                                                                            Combined thoraco-laparoscopy for trans-diaphragmatic thoraco-abdominal enteric duplications

                                                                            Journal of Pediatric Surgery
                                                                            Vol. 40Issue 9e37–e40Published in issue: September, 2005
                                                                            • Marcelo Martinez-Ferro
                                                                            • Pablo Laje
                                                                            • Lisandro Piaggio
                                                                            Cited in Scopus: 12
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                                                                              During the last years, several thoracic and abdominal enteric duplications were resected in our institution by means of minimally invasive approaches [Rev Cir Infantil 1999;9(2):113-115]. Our last patient, however, had a giant thoraco-abdominal duodenal duplication, extending from the upper thoracic cavity to the pelvis, in a dumbbell fashion. Forty days after birth, a combined “thoraco-laparoscopy” was performed, achieving a complete resection of the cyst. The diaphragmatic defect was repaired as well.
                                                                              Combined thoraco-laparoscopy for trans-diaphragmatic thoraco-abdominal enteric duplications
                                                                            • Rapid Communication

                                                                              Laparoscopic patch repair of diaphragmatic hernias with Surgisis

                                                                              Journal of Pediatric Surgery
                                                                              Vol. 40Issue 8e1–e5Published in issue: August, 2005
                                                                              • George W. Holcomb III
                                                                              • Daniel J. Ostlie
                                                                              • Kelly A. Miller
                                                                              Cited in Scopus: 48
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                                                                                Laparoscopic repair of congenital diaphragmatic hernias has been sparsely reported. Moreover, each report has primarily been a single operative case. In most of the reports, prosthetic mesh has not been used, and when used, it has been nonabsorbable in nature. Most of these case reports have documented only a few months of clinical follow-up.
                                                                                Laparoscopic patch repair of diaphragmatic hernias with Surgisis
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