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Journal of Pediatric Surgery
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    Article Type

    • Rapid Communication8

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    Author

    • Auber, Frédéric1
    • Barnett, Sean J1
    • Boutelle, Kerri N1
    • Bowley, Douglas M1
    • Bracco, Gian Luca1
    • Casillas, Javier1
    • Chabaud-Williamson, Maud1
    • Chang, Yu-Tang1
    • Ciancio, Gaetano1
    • Coccia, Maria Elisabetta1
    • Coulomb-L'herminé, Aurore1
    • Durkin, Emily T1
    • Fasola, Sylvie1
    • Harrison, Andrew R1
    • Hendrickse, Charles1
    • Huang, Chein-Lin1
    • Ikramuddin, Sayeed1
    • Kellogg, Todd A1
    • Kini, Hema1
    • Kotobi, Henri1
    • Lee, Jui-Ying1
    • Leslie, Daniel B1
    • Mathai, Alka Mary1
    • Mistry, Pritesh1
    • Murali, Nirupama1

    Journal

    • Journal of Pediatric Surgery8

    Keyword

    • Laparoscopy2
    • Blunt duodenal injury1
    • Breast mass1
    • CCAM type 11
    • Cloacogenic polyps1
    • Cyst1
    • Emphysema1
    • Glomus tumor1
    • Gynecomastia1
    • Intraductal papilloma1
    • Kidney1
    • Laparoscopic Roux-en-Y gastric bypass1
    • Lung1
    • Male1
    • Mature teratoma1
    • Mucinous cystadenoma1
    • Multilobar1
    • Nephron-sparing surgery1
    • Ovarian-sparing surgery1
    • Ovary1
    • Perforation1
    • Pseudotumor cerebri1
    • Rectal bleeding1
    • Severe obesity1

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    • Rapid Communication

      Cloacogenic polyps in an adolescent: A rare cause of rectal bleeding

      Journal of Pediatric Surgery
      Vol. 48Issue 8e5–e7Published in issue: August, 2013
      • Shafquat Zaman
      • Pritesh Mistry
      • Charles Hendrickse
      • Douglas M. Bowley
      Cited in Scopus: 3
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        Cloacogenic polyps are rare inflammatory lesions occurring around the anal transitional zone and in the lower rectum which can mimic neoplasia. They should be given diagnostic consideration in patients presenting with symptoms of rectal bleeding, tenesmus, and altered bowel habits.
        Cloacogenic polyps in an adolescent: A rare cause of rectal bleeding
      • 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

          Enlarging unilateral breast mass in an adolescent male: an unusual presentation of intraductal papilloma

          Journal of Pediatric Surgery
          Vol. 46Issue 5e33–e35Published in issue: May, 2011
          • Emily T. Durkin
          • Thomas F. Warner
          • Peter F. Nichol
          Cited in Scopus: 14
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            Breast masses presenting in adolescent boys are rare and are almost uniformly owing to gynecomastia. Although surgical referral for breast masses in adolescent boys is common, intervention is typically for cosmesis. We report the case of a 14-year-old boy who presented with an enlarging unilateral breast mass, which was found to be owing to an intraductal papilloma at the time of surgical excision.
            Enlarging unilateral breast mass in an adolescent male: an unusual presentation of intraductal papilloma
          • Rapid Communication

            Mucinous cystadenoma arising 3 years after ovarian-sparing surgery for mature teratoma in a child

            Journal of Pediatric Surgery
            Vol. 45Issue 8e9–e12Published in issue: August, 2010
            • Benoit Parmentier
            • Emmanuelle Vaz
            • Maud Chabaud-Williamson
            • Sylvie Fasola
            • Henri Kotobi
            • Aurore Coulomb-L'herminé
            • and others
            Cited in Scopus: 11
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              We report the case of a 15-year-old girl diagnosed with mucinous cystadenoma 3 years after ovarian-sparing surgery for a mature teratoma located in the same ovary. Ovarian teratoma is the most common ovarian neoplasm in children, whereas mucinous cystadenoma is extremely rare during childhood.
              Mucinous cystadenoma arising 3 years after ovarian-sparing surgery for mature teratoma in a child
            • Rapid Communication

              Renal glomus tumor in an adolescent: a conservative approach

              Journal of Pediatric Surgery
              Vol. 45Issue 6e23–e26Published in issue: June, 2010
              • Zaher Nuwayhid
              • Maria M. Rodriguez
              • Angela Prescott
              • Gaetano Ciancio
              • Claudia P. Rojas
              • Javier Casillas
              • and others
              Cited in Scopus: 5
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                The most common renal neoplasms in the second decade of life are renal cell carcinomas and Wilms' tumors. Glomus tumors arising in the kidney are rare. We report an adolescent with a benign renal glomus tumor excised by wedge resection. Nephron-sparing surgery is the therapy of choice for children with benign renal tumors. Glomus tumor should be considered in the differential diagnosis of a renal mass in a young patient.
                Renal glomus tumor in an adolescent: a conservative approach
              • Rapid Communication

                Congenital cystic adenomatoid malformation of lung type 1

                Journal of Pediatric Surgery
                Vol. 45Issue 2e25–e28Published in issue: February, 2010
                • Alka Mary Mathai
                • Hema Kini
                • Muktha R. Pai
                • Ashok B. Shetty
                • Nirupama Murali
                Cited in Scopus: 6
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                  Congenital cystic adenomatoid malformation, a rare developmental, hamartomatous abnormality of the lung, usually is unilateral, is localized, and presents in early infancy. Delayed occurrence in older children and multilobar involvement are rare. We describe a case of congenital cystic adenomatoid malformation type 1 with multilobar involvement, associated emphysema, and coexistent tracheobronchopathia osteochondroplastica in an adolescent girl for whom the correct diagnosis was achieved only on histologic examination.
                  Congenital cystic adenomatoid malformation of lung type 1
                • 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

                    Preserved vision without growth retardation after laparoscopic Roux-en-Y gastric bypass in a morbidly obese child with pseudotumor cerebri: 36-month follow-up

                    Journal of Pediatric Surgery
                    Vol. 43Issue 7e27–e30Published in issue: July, 2008
                    • Daniel B. Leslie
                    • Todd A. Kellogg
                    • Kerri N. Boutelle
                    • Sean J. Barnett
                    • Sarah J. Schwarzenberg
                    • Andrew R. Harrison
                    • and others
                    Cited in Scopus: 11
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                      A 12-year-old boy presented with a weight of 136 kg and a history of progressive vision loss associated with unremitting pseudotumor cerebri requiring bilateral optic nerve sheath decompression. He underwent laparoscopic Roux-en-Y gastric bypass (RYGBP) without complication. At 36 months post-RYGBP, he has grown 5 cm since the time of surgery, his weight is 6.8 kg above his postoperative nadir weight of 68.2 kg, and his visual acuity has improved with OD 20/100 (preoperative, 20/200) and OS 20/70 (preoperative, 20/100).
                      Preserved vision without growth retardation after laparoscopic Roux-en-Y gastric bypass in a morbidly obese child with pseudotumor cerebri: 36-month follow-up
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