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dc.contributor.authorGarzi, Alfredo
dc.contributor.authorPrestipino, Marco
dc.contributor.authorRubino, Maria Serena
dc.contributor.authorCalabrò, Eleonora
dc.date.accessioned2020-07-08T09:45:34Z
dc.date.available2020-07-08T09:45:34Z
dc.date.created2020
dc.identifier.citationGarzi A, Prestipino M, Rubino MS, Calabrò E. Surgical vls therapy of oesophageal achalasia in pediatric age: four case reports. Translational Medicine @ UniSa 2020, 22(9): 38-43.it_IT
dc.identifier.issn2239-9747it_IT
dc.identifier.urihttp://www.translationalmedicine.unisa.it/indexit_IT
dc.identifier.urihttp://elea.unisa.it:8080/xmlui/handle/10556/4628
dc.identifier.urihttp://dx.doi.org/10.14273/unisa-2817
dc.description.abstractThe Authors present a retrospective review of their record of cases, characterized by 4 cases of achalasia in which it was performed a Heller myotomy with front fundoplication (Thall) in laparoscopic approach in the period from 2012 to 2019. In paediatric achalasia, the laparoscopic Heller myotomy seems to be the best treatment because of its multiple advantages offered by the minimally invasive technique. First of all, thanks to the video-technique, which allows a complete and extended myotomy, the accuracy of this operation is maximized; moreover, the post-operative pain is widely reduced, thanks to the minimal dissection and traction of the tissues; finally, but not negligible, this approach ensures a better aesthetic result than the classic open technique. With regard to the front fundoplication, the Authors suggest that it is mandatory because, even if it extends the operating time, it ensures a natural protection to the myotomy herniated mucosa and avoids gastro-oesophageal reflux, which often occurs after the surgical correction, thus obliging to perform a reoperation.it_IT
dc.format.extentP. 38-43it_IT
dc.language.isoenit_IT
dc.sourceUniSa. Sistema Bibliotecario di Ateneoit_IT
dc.subjectAchalasiait_IT
dc.subjectPediatric ageit_IT
dc.subjectLaparoscopic approachit_IT
dc.titleSurgical vls therapy of oesophageal achalasia in pediatric age: four case reportsit_IT
dc.typeArticleit_IT
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