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- Ahn, Kang Mo1
- Alaish, Samuel M1
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- Baudraz-Rosselet, Florence1
- Borgi, Aida1
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- Fabio Fonseca Simoes1
- Fatureto, Marcelo Cunha1
- Fayad, Laura M1
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- Green, Holly L1
- Gunduz, Ergun1
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Keyword
- Child2
- Anesthesia1
- Bicipital rib1
- Brachial plexus1
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- Desmoplastic small round cell tumor1
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Online Exclusives
11 Results
- Research Article
Brachial plexus palsy, a rare delayed complication of the Nuss procedure for pectus excavatum: a case report
Journal of Pediatric SurgeryVol. 47Issue 11e19–e20Published in issue: November, 2012- Tieqin Liu
- Hongxu Liu
- Chunlu Yang
- Shun Xu
- Changbo Sun
Cited in Scopus: 3We 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 SurgeryVol. 47Issue 8e33–e35Published in issue: August, 2012- Ilhan Ciftci
- Seza Apiliogullari
- Inci Kara
- Ergun Gunduz
- Ates Duman
Cited in Scopus: 3Duodenal 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. - Rapid Communication
Invasive thymoma in a child: a rare case report
Journal of Pediatric SurgeryVol. 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: 4Thymomas 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. - Rapid Communication
Toxic epidermal necrolysis complicated by small bowel intussusception: a case report
Journal of Pediatric SurgeryVol. 46Issue 2e9–e11Published in issue: February, 2011- Asma Bouziri
- Ammar Khaldi
- Asma Hamdi
- Aida Borgi
- Sofiene Ghorbel
- Monia Kharfi
- and others
Cited in Scopus: 7Intestinal 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. - Rapid Communication
Modified technique of meso-Rex shunt in case of insufficient length of the jugular vein graft
Journal of Pediatric SurgeryVol. 44Issue 11e9–e12Published in issue: November, 2009- Christophe Chardot
- Alexandre Darani
- Remi Dubois
- Pierre-Yves Mure
- Jean-Pierre Pracros
- Alain Lachaux
Cited in Scopus: 9Meso-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. - Rapid Communication
Primary intestinal lymphangiectasia successfully treated by segmental resections of small bowel
Journal of Pediatric SurgeryVol. 44Issue 10e13–e17Published in issue: October, 2009- Na Rae Kim
- Suk-Koo Lee
- Yeon-Lim Suh
Cited in Scopus: 16Primary 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. - Rapid Communication
Glial heterotopia of the face
Journal of Pediatric SurgeryVol. 43Issue 12e1–e3Published in issue: December, 2008- Laurent Riffaud
- Rémy Ndikumana
- Olivier Azzis
- Bernard Cadre
Cited in Scopus: 10The 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. - Rapid Communication
Symptomatic anterior sternoclavicular joint secondary to a Bicipital rib
Journal of Pediatric SurgeryVol. 43Issue 10e23–e26Published in issue: October, 2008- Samuel M. Alaish
- F. Dylan Stewart
- Laura M. Fayad
Cited in Scopus: 1This 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. - Rapid Communication
Tinea capitis: no incision nor excision
Journal of Pediatric SurgeryVol. 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: 26Tinea 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. - Rapid Communication
Continuous hyperthermic peritoneal perfusion for desmoplastic small round cell tumor
Journal of Pediatric SurgeryVol. 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: 41Desmoplastic 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. - Research Article
Complete surgical resection of inflammatory myofibroblastic tumor with carinal reconstruction in a 4-year-old boy
Journal of Pediatric SurgeryVol. 40Issue 12e23–e25Published in issue: December, 2005- I Hoseok
- Han Joungho
- Kang Mo Ahn
- Sang Il Lee
- Kim Jhingook
Cited in Scopus: 19Inflammatory 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.