2013
DOI: 10.1016/j.jpedsurg.2013.07.019
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Esophageal Atresia: Gastroesophageal functional follow-up in 5–15year old children

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Cited by 84 publications
(102 citation statements)
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References 68 publications
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“…According to van Wijk et al [23], transient lower esophageal sphincter relaxation was the most common mechanism underlying gastroesophageal reflux disease in infants, delayed bolus clearance and delayed gastric emptying. Besides esophagitis, Barrett esophagus and adenocarcinoma may also develop [17,24,25]. In our study, in one child, gastric metaplasia was present in the lower part of the esophagus.…”
Section: Discussionmentioning
confidence: 52%
“…According to van Wijk et al [23], transient lower esophageal sphincter relaxation was the most common mechanism underlying gastroesophageal reflux disease in infants, delayed bolus clearance and delayed gastric emptying. Besides esophagitis, Barrett esophagus and adenocarcinoma may also develop [17,24,25]. In our study, in one child, gastric metaplasia was present in the lower part of the esophagus.…”
Section: Discussionmentioning
confidence: 52%
“…It is secondary to esophageal dysmotility, short esophagus, lower esophageal sphincter pressure, and chronic lung disease. 4,17,18 Dysmotility is the result of intrinsic factors related to abnormal esophagus development or partial denervation during surgery. Motor patterns were described in a cohort of children with EA using a high resolution manometry.…”
Section: Esophageal Atresiamentioning
confidence: 99%
“…The treatment of choice is surgical repair with potential late complications such as dysphagia, gastroesophageal reflux, strictures, and dysmotility. [3][4][5] An increased risk of EoE has been described in patients with successful repair of EA secondary to gastroesophageal reflux disease (GERD), esophageal dysmotility, and the genetic similarities common to both conditions: the mutations in the Forkhead box (FOX) gene cause congenital anomalies, such as EA. In addition, FOXF1 genes are present in the promoter region of inflammation, including eotaxin-3, which is increased in EoE; therefore, Gorter et al proposed that patients with EA may have a greater risk for developing EoE.…”
Section: Introductionmentioning
confidence: 99%
“…Es secundaria a dismotilidad esofágica, un esófago corto, disminución de la presión del esfínter esofágico inferior y enfermedad pulmonar crónica. 4,17,18 La dismotilidad se debe a factores intrínsecos relacionados con el desarrollo anormal del esófago o con la denervación parcial durante la cirugía. Los patrones motores fueron descritos en una cohorte de niños con AE usando manometría de alta resolución.…”
Section: Atresia De Esófagounclassified
“…El tratamiento de elección es la corrección quirúrgica, con posibles complicaciones alejadas, como disfagia, reflujo gastroesofágico, estenosis y dismotilidad. [3][4][5] Se ha descrito un riesgo aumentado de EEo en pacientes con AE corregida secundario a enfermedad por reflujo gastroesofágico (ERGE), dismotilidad esofágica y a las similitudes genéticas que comparten ambas patologías: mutaciones en el gen Forkhead box (FOX) producen anomalías congénitas, como AE. Además, los genes FOXF1 están presentes en la región promotora de inflamación, que incluyen eotaxina-3, la cual está proponen que los pacientes con AE podrían tener mayor posibilidad de desarrollar EEo.…”
Section: Introductionunclassified