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Journal of Pediatric Surgery
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    Article Type

    • Rapid Communication9
    • Research Article2

    Publication Date

    Author

    • Ahn, Kang Mo1
    • Alaish, Samuel M1
    • Anderson, Pete1
    • Apiliogullari, Seza1
    • Azzis, Olivier1
    • Baudraz-Rosselet, Florence1
    • Borgi, Aida1
    • Bouziri, Asma1
    • Cadre, Bernard1
    • Carrara, Guilherme Freire Angotti1
    • Chardot, Christophe1
    • Ciftci, Ilhan1
    • Curley, Steven1
    • Darani, Alexandre1
    • Dubois, Remi1
    • Duman, Ates1
    • Dushi, Gezim1
    • Etchebehere, Renata Margarida1
    • Fabio Fonseca Simoes1
    • Fatureto, Marcelo Cunha1
    • Fayad, Laura M1
    • Ghorbel, Sofiene1
    • Green, Holly L1
    • Gunduz, Ergun1
    • Hadj, Sarra Bel1

    Journal

    • Journal of Pediatric Surgery11

    Keyword

    • Child2
    • Anesthesia1
    • Bicipital rib1
    • Brachial plexus1
    • Carinatum1
    • Chest wall1
    • Childhood1
    • Children1
    • Complications1
    • Congenital anomaly1
    • Congenital malformation1
    • Desmoplastic small round cell tumor1
    • Duodenal atresia1
    • Glial heterotopia1
    • Hyperthermic perfusion1
    • Injury1
    • Intestinal obstruction1
    • Kerion1
    • Lymphangiectasis, Intestinal1
    • Mediastinum tumor1
    • Nasal glioma1
    • Parenteral nutrition1
    • Pectus excavatum1
    • Pediatric1

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    • Research Article

      Brachial plexus palsy, a rare delayed complication of the Nuss procedure for pectus excavatum: a case report

      Journal of Pediatric Surgery
      Vol. 47Issue 11e19–e20Published in issue: November, 2012
      • Tieqin Liu
      • Hongxu Liu
      • Chunlu Yang
      • Shun Xu
      • Changbo Sun
      Cited in Scopus: 3
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        We report a rare complication after the Nuss procedure for the correction of pectus excavatum in a 15-year-old adolescent boy. He began to have delayed right brachial plexus injury on the 15th postoperative day. Careful physical check-up revealed a painful and enlarged subaxillary lymph node. He was successfully treated using anti-inflammatory medications and physical therapy.
      • Rapid Communication

        Repair of duodenal atresia under spinal anesthesia in a low-birth-weight preterm neonate: case report

        Journal of Pediatric Surgery
        Vol. 47Issue 8e33–e35Published in issue: August, 2012
        • Ilhan Ciftci
        • Seza Apiliogullari
        • Inci Kara
        • Ergun Gunduz
        • Ates Duman
        Cited in Scopus: 3
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          Duodenal atresia is a well-recognized cause of neonatal bowel obstruction. General anesthesia with tracheal intubation is the traditional anesthetic technique for surgical correction of this condition. Metabolic abnormalities and fluid deficits coupled with residual anesthetics are known to increase the risk of postoperative apnea, prolonging the operating room time and delaying extubation. Spinal anesthesia (SA) is an accepted alternative to general anesthesia in formerly preterm infants. In the current literature, there are reports of successful use of SA for simple infraumbilical surgery and, occasionally, for upper abdominal surgery, but there is no information on the use of SA in neonates for duodenal atresia repair.
          Repair of duodenal atresia under spinal anesthesia in a low-birth-weight preterm neonate: case report
        • Rapid Communication

          Invasive thymoma in a child: a rare case report

          Journal of Pediatric Surgery
          Vol. 47Issue 2e23–e25Published in issue: February, 2012
          • Mauricio Murce Rocha
          • Precil Diego Miranda de Menezes Neves
          • Camila Cristina Martini Rodrigues
          • Guilherme Freire Angotti Carrara
          • Fábio Fonseca Simões
          • Renata Margarida Etchebehere
          • and others
          Cited in Scopus: 4
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            Thymomas are neoplasms of the anterior mediastinum and generally occur between the fourth and sixth decades of life. In children, they are rare, with few reported cases. We describe a 9-year-old boy with invasive thymoma treated successfully by surgery alone. The patient was previously healthy and under treatment for a community-acquired pneumonia. A chest radiograph showed an opacity at the left lung base, and thoracic computed tomographic scan showed a mass with thick walls and liquid content situated in the lingula with no cleavage plane with the mediastinum.
            Invasive thymoma in a child: a rare case report
          • Rapid Communication

            Toxic epidermal necrolysis complicated by small bowel intussusception: a case report

            Journal of Pediatric Surgery
            Vol. 46Issue 2e9–e11Published in issue: February, 2011
            • Asma Bouziri
            • Ammar Khaldi
            • Asma Hamdi
            • Aida Borgi
            • Sofiene Ghorbel
            • Monia Kharfi
            • and others
            Cited in Scopus: 7
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              Intestinal involvement in toxic epidermal necrolysis (TEN) has been identified only rarely. We report a case of TEN complicated by small bowel intussusception. The patient was a previously healthy 8-year-old boy who presented with TEN and extensive lesions, including up to 40% of the body surface area as well as conjunctival, oropharyngeal, respiratory, and genital mucosa. Rapidly after the onset of a constant rate of enteral feeding, he developed bilious vomiting, diarrhea, and significant abdominal distension.
              Toxic epidermal necrolysis complicated by small bowel intussusception: a case report
            • Rapid Communication

              Modified technique of meso-Rex shunt in case of insufficient length of the jugular vein graft

              Journal of Pediatric Surgery
              Vol. 44Issue 11e9–e12Published in issue: November, 2009
              • Christophe Chardot
              • Alexandre Darani
              • Remi Dubois
              • Pierre-Yves Mure
              • Jean-Pierre Pracros
              • Alain Lachaux
              Cited in Scopus: 9
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                Meso-Rex shunt (MRS) can relieve portal hypertension and restore a physiological portal flow in patients with portal vein thrombosis. We describe a technical variant where the autologous internal jugular vein (IJV) was too short to bridge the superior mesenteric vein (SMV) and the Rex recessus.
                Modified technique of meso-Rex shunt in case of insufficient length of the jugular vein graft
              • Rapid Communication

                Primary intestinal lymphangiectasia successfully treated by segmental resections of small bowel

                Journal of Pediatric Surgery
                Vol. 44Issue 10e13–e17Published in issue: October, 2009
                • Na Rae Kim
                • Suk-Koo Lee
                • Yeon-Lim Suh
                Cited in Scopus: 16
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                  Primary intestinal lymphangiectasia is a rare cause of protein-losing enteropathy and usually presents with intermittent diarrhea or malnutrition. Diagnosis depends largely on its pathologic condition demonstrating greatly dilated lymphatics mainly in the lamina propria of the mucosa. We report a case of primary intestinal lymphangiectasia, of the diffuse type, presenting with abdominal pain and voluminous diarrhea in a previously healthy 8-year-old boy. He had periumbilical pain for 3 months before presentation.
                  Primary intestinal lymphangiectasia successfully treated by segmental resections of small bowel
                • Rapid Communication

                  Glial heterotopia of the face

                  Journal of Pediatric Surgery
                  Vol. 43Issue 12e1–e3Published in issue: December, 2008
                  • Laurent Riffaud
                  • Rémy Ndikumana
                  • Olivier Azzis
                  • Bernard Cadre
                  Cited in Scopus: 10
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                    The authors report a case of combined subcutaneous and intranasal glial heterotopia of the face in a 4-month-old boy. The pathogenesis and differential diagnoses of this rare developmental disorder are discussed as is the importance of careful radiologic findings for appropriate surgical decision.
                    Glial heterotopia of the face
                  • Rapid Communication

                    Symptomatic anterior sternoclavicular joint secondary to a Bicipital rib

                    Journal of Pediatric Surgery
                    Vol. 43Issue 10e23–e26Published in issue: October, 2008
                    • Samuel M. Alaish
                    • F. Dylan Stewart
                    • Laura M. Fayad
                    Cited in Scopus: 1
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                      This case report details the diagnosis and treatment of a previously unreported complication of a congenital chest wall anomaly. Our patient presented with a painful anterior sternoclavicular joint subluxation secondary to a bicipital rib. Thoracic magnetic resonance and computed tomographic imaging provided the diagnosis. Complete resolution of symptoms was achieved after resection of the bicipital rib.
                      Symptomatic anterior sternoclavicular joint secondary to a Bicipital rib
                    • Rapid Communication

                      Tinea capitis: no incision nor excision

                      Journal of Pediatric Surgery
                      Vol. 42Issue 8e33–e36Published in issue: August, 2007
                      • Laetitia von Laer Tschudin
                      • Emmanuel Laffitte
                      • Florence Baudraz-Rosselet
                      • Gezim Dushi
                      • Judith Hohlfeld
                      • Anthony S. de Buys Roessingh
                      Cited in Scopus: 26
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                        Tinea capitis is a fungal infection of the scalp and hair shaft that mainly affects prepubescent children. Its clinical aspects range from a mild noninflammatory infection resembling seborrheic dermatitis to a highly inflammatory swelling reaction (kerion). We report the cases of 2 children who underwent surgical treatment of their kerions under general anesthesia. One lesion had been incised and the other excised. This inappropriate treatment made conservative treatment after surgery more difficult.
                        Tinea capitis: no incision nor excision
                      • Rapid Communication

                        Continuous hyperthermic peritoneal perfusion for desmoplastic small round cell tumor

                        Journal of Pediatric Surgery
                        Vol. 42Issue 8e29–e32Published in issue: August, 2007
                        • Andrea Hayes-Jordan
                        • Pete Anderson
                        • Steven Curley
                        • Cynthia Herzog
                        • Kevin P. Lally
                        • Holly L. Green
                        • and others
                        Cited in Scopus: 41
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                          Desmoplastic small round cell tumor (DSRCT) is a rare disease of children, adolescents, and young adults that begins and spreads on the peritoneal surfaces. Desmoplastic small round cell tumor usually presents with diffuse abdominal metastatic disease similar in gross appearance to carcinomatosis. To date, very aggressive treatment programs have yielded dismal outcomes. Here we present 2 cases of DSRCT that were treated with aggressive surgical excision followed by intraoperative continuous hyperthermic peritoneal perfusion using cisplatin.
                          Continuous hyperthermic peritoneal perfusion for desmoplastic small round cell tumor
                        • Research Article

                          Complete surgical resection of inflammatory myofibroblastic tumor with carinal reconstruction in a 4-year-old boy

                          Journal of Pediatric Surgery
                          Vol. 40Issue 12e23–e25Published in issue: December, 2005
                          • I Hoseok
                          • Han Joungho
                          • Kang Mo Ahn
                          • Sang Il Lee
                          • Kim Jhingook
                          Cited in Scopus: 19
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                            Inflammatory myofibroblastic tumor of the carina and the main bronchus is a rare tumor. The authors report here on a case of a 4-year-old boy with an inflammatory myofibroblastic tumor at the carina and extending to the left main bronchus. He presented with fever and a cough of 2 months' duration. Preoperative assessment of the tumor revealed an intraluminal round mass arising from the carina and extending into the left main bronchus, and this caused near-total obstruction of the left main bronchus and the subsequent total collapse of the entire left lung.
                            Complete surgical resection of inflammatory myofibroblastic tumor with carinal reconstruction in a 4-year-old boy
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