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Pathomorphological Changes Developing in the Stenosing Variant of Esophageal Atresia in Infants

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dc.contributor.author Erkin A. Eshbaev1, Aziz A. Zufarov2, Makhzuna Kh. Mukhsinova3,
dc.date.accessioned 2025-05-24T15:16:19Z
dc.date.available 2025-05-24T15:16:19Z
dc.date.issued 2025
dc.identifier.uri http://repo.tma.uz/xmlui/handle/1/1649
dc.description.abstract Although the clinical and morphological frequency of atresia, which is the 4th variant of esophageal malformation and continues mainly with esophageal wall stenosis, is relatively low, in most cases patients experience a sudden decrease in quality of life. Morphologically, all anatomical walls of the esophagus of this type contain formed tissue components mainly in those areas that have not undergone stenosis, and in those areas where stenosis is detected, areas that have undergone dysplasia in the esophageal wall are identified. In particular, myodysplasia on the muscular bottoms is characterized by the fact that there are very few alveolar tubular glands on the mucosa and mucous membranes, there are 1-3-layered cuboid and prismatic epithelium on the surface of the mucous membrane, as well as cuboid epithelium cells that undergo metaplasia. en_US
dc.language.iso en_US en_US
dc.publisher American Journal of Medicine and Medical Sciences en_US
dc.subject Esophageal atresia, Stenosis, Morphology, Dysplasia, Morphological paralysis en_US
dc.title Pathomorphological Changes Developing in the Stenosing Variant of Esophageal Atresia in Infants en_US
dc.type Article en_US


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