{"title":"先天性膈疝患者的前肠重复囊肿一例报告。","authors":"Aleksandra I Sadecka, Zaneta Slowik-Moczydlowska","doi":"10.7759/cureus.86349","DOIUrl":null,"url":null,"abstract":"<p><p>Esophageal duplication cysts are a rare form of foregut developmental abnormality with heterogeneous manifestations due to their variable location and size. Congenital diaphragmatic hernia is a congenital defect resulting from incomplete diaphragm formation, with a wide spectrum of severity. It is typically diagnosed antenatally and managed surgically in the neonatal period. We present a case report of a newborn with a rare co-occurrence of congenital diaphragmatic hernia and multiple esophageal duplication cysts.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"17 6","pages":"e86349"},"PeriodicalIF":1.3000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12178452/pdf/","citationCount":"0","resultStr":"{\"title\":\"Foregut Duplication Cysts in a Patient With Congenital Diaphragmatic Hernia: A Case Report.\",\"authors\":\"Aleksandra I Sadecka, Zaneta Slowik-Moczydlowska\",\"doi\":\"10.7759/cureus.86349\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Esophageal duplication cysts are a rare form of foregut developmental abnormality with heterogeneous manifestations due to their variable location and size. Congenital diaphragmatic hernia is a congenital defect resulting from incomplete diaphragm formation, with a wide spectrum of severity. It is typically diagnosed antenatally and managed surgically in the neonatal period. We present a case report of a newborn with a rare co-occurrence of congenital diaphragmatic hernia and multiple esophageal duplication cysts.</p>\",\"PeriodicalId\":93960,\"journal\":{\"name\":\"Cureus\",\"volume\":\"17 6\",\"pages\":\"e86349\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2025-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12178452/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cureus\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7759/cureus.86349\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cureus","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7759/cureus.86349","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Foregut Duplication Cysts in a Patient With Congenital Diaphragmatic Hernia: A Case Report.
Esophageal duplication cysts are a rare form of foregut developmental abnormality with heterogeneous manifestations due to their variable location and size. Congenital diaphragmatic hernia is a congenital defect resulting from incomplete diaphragm formation, with a wide spectrum of severity. It is typically diagnosed antenatally and managed surgically in the neonatal period. We present a case report of a newborn with a rare co-occurrence of congenital diaphragmatic hernia and multiple esophageal duplication cysts.
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