Gastroscopic treatment of membranous duodenal stenosis in infants and children: Report of 6 cases

Huang, Maohua; Bian, Hongqiang; Liang, Chong; Wei, Wei; Duan, Xu; Yang, Jun

doi:10.1016/j.jpedsurg.2014.10.045

Cited by 34 publications

(33 citation statements)

References 8 publications

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“…In particular, only a few CDS patients associated with SI have ever been reported before [2]. Although there are some reports of gastroscopic treatment for membranous duodenal stenosis, we selected open surgery because the location of the papilla Vater could not be identified in our case [5, 8]. …”

Section: Discussionmentioning

confidence: 99%

“…Congenital duodenal obstruction, which includes atresia and stenosis, is estimated to have an incidence of about 1 in 4,000 to 15,000 live births [2, 3]. Congenital duodenal stenosis (CDS) is relatively rare in comparison with duodenal atresia and sometimes has a delayed presentation [3–5]. CDS associated with SI is an extremely rare entity and only a few cases have been reported thus far [2, 6].…”

Section: Introductionmentioning

confidence: 99%

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Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Saeki

Ueno²,

Mukai³

et al. 2017

Case Reports in Pediatrics

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Background. Situs inversus is a rare congenital anomaly with a reported incidence of only 1 in 5,000 to 10,000 live births. Congenital duodenal stenosis complicated with situs inversus is an even rarer entity. Case Presentation. A 1-year-old girl with situs inversus who had undergone a hemi-Fontan procedure against a single ventricle in our hospital was referred to our department for vomiting and failure to thrive. An upper gastrointestinal contrast study and endoscopy revealed duodenal stenosis. A transumbilical radical operation as a minimally invasive surgery was successfully performed. After the surgery, she stopped vomiting, and the postoperative course was uneventful with good cosmetic results. Conclusions. To our knowledge, this is the first report of transumbilical surgery for congenital duodenal stenosis with situs inversus as minimally invasive surgery. Transumbilical surgery to situs inversus patient can be performed safely and lead to good cosmetic outcome.

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Section: Discussionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Saeki

Ueno²,

Mukai³

et al. 2017

Case Reports in Pediatrics

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“…Web) oder Atresien mit inkomplettem Web, die auch erst jenseits der Neonatalperiode auffallen können, können endoskopisch mittels Ballondilatation und einem endoskopisch eingeführten Elektrokauter erfolgreich therapiert werden [15]. Diese Methode konnte schon bei Neugeborenen angewendet werden [16].…”

Section: Endoskopische Therapie Duodenaler Websunclassified

Innovative Techniken in der Gastroenterologie

Broekaert¹,

Töx²,

Hünseler³

2019

Pädiatrie up2date

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“…El primer reporte de una membranectomía realizada por vía endoscópica fue en 1989, donde se describe el uso exitoso de ondas de alta frecuencia para realizar un corte "en T" de la membrana duodenal (24) . En la literatura se describen casos de resolución endoscópica en pacientes de tan solo 7 días de vida (25) . Existen reportes con excelentes resultados pronósticos en los que se realizaron tanto secciones longitudinales como circunferenciales de membranas duodenales, así como también casos en los que se realizaron secciones radiales de la membrana, con resultados promisorios (26) (27) .…”

Section: 25184/anfamed2017v4n2a7unclassified

Membrana duodenal: a propósito de un caso

Ormaechea¹,

Berazategui²

2017

An Facultad Med

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La atresia de duodeno es una causa poco frecuente de oclusión intestinal. Generalmente el diagnósti-co se realiza en etapa prenatal o en el período neonatal principalmente para aquellos casos de oclusión completa, mientras que aquellos con oclusión incompleta pueden diagnosticarse más tardíamente. Se presenta el caso clínico de una paciente con una forma de presentación infrecuente, con diagnóstico luego del año de vida. Se realizó una duodeno anastomosis, con buena evolución postoperatoria. Palabras claveAtresia de duodeno, membrana duodenal. AbstractDuodenal atresia is a rare cause of intestinal occlusion. Generally, the diagnosis is made in the prenatal stage or in the neonatal period mainly for those cases of complete occlusion, whereas those with incomplete occlusion may be diagnosed later. We present the case of a patient with an uncommon presentation, with diagnosis after one year of life. A duodenum-duodenum anastomosis was performed, with good postoperative evolution. Key WordsDuodenal atresia, duodenal membrane. ResumoA atresia duodenal é uma causa rara de oclusão intestinal. O diagnóstico geralmente é feito no estágio pré-natal ou no período neonatal principalmente para os casos de oclusão completa, enquanto aqueles com oclusão incompleta podem ser diagnosticados mais tarde. Apresentamos o caso de uma paciente com uma apresentação incomum, com diagnóstico após o ano de vida. Uma anastomose duodeno foi realizada, com boa evolução pós-operatória.

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Gastroscopic treatment of membranous duodenal stenosis in infants and children: Report of 6 cases

Cited by 34 publications

References 8 publications

Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Innovative Techniken in der Gastroenterologie

Membrana duodenal: a propósito de un caso

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