{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,30]],"date-time":"2026-08-30T15:33:24Z","timestamp":1788104004553,"version":"build-2803163510"},"reference-count":12,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"C","license":[{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2025,1,1]],"date-time":"2025-01-01T00:00:00Z","timestamp":1735689600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,11,25]],"date-time":"2024-11-25T00:00:00Z","timestamp":1732492800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2025,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Introduction and importance:<\/jats:title>\n                    <jats:p>Intestinal atresia is a congenital condition characterized by the blockage or constriction of an intestine portion. It is caused by either a vascular issue or a failure of recanalization during fetal development. Surgery is essential for both a definitive diagnosis and therapy.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Case presentation:<\/jats:title>\n                    <jats:p>A preterm neonate (gestational age 34 weeks) was delivered by cesarean section due to polyhydramnios and complained of recurrent episodes of non-bilious vomiting after breastfeeding. Prenatal ultrasound revealed a double bubble sign, indicating intestinal atresia, while on contrast imaging, the contrast was refluxed from the stomach to the esophagus, the absence of gases in the intestine or colon suggested a gastric outlet obstruction. The atretic intestine was identified during laparotomy, from the second section of the duodenum to the rectum with no lumen. There were no surgical options available. Atresia is typically treated by excision and anastomosis of the remaining normal canalized intestine. However, in our case, a total intestinal atresia was discovered, and no intestinal lumen was identified to undergo surgery.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Clinical discussion:<\/jats:title>\n                    <jats:p>It was found that the atretic intestine in our case extended from the duodenum to the rectum. However, in the two previously documented cases of atresia, the atresia began in the jejunum and progressed to the rectum in one instance and the sigmoid colon in the other.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>Because there were no alternative surgical options, the intestine was relocated, and the abdomen was closed. Such cases require more sensitive diagnostic instruments to recognize, and probable etiologies should be researched further to prevent them.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Highlights<\/jats:title>\n                  <\/jats:sec>","DOI":"10.1016\/j.ijscr.2024.110668","type":"journal-article","created":{"date-parts":[[2024,11,29]],"date-time":"2024-11-29T22:55:09Z","timestamp":1732920909000},"update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":3,"title":["Total intestinal atresia with failure of recanalization extending from the duodenum to the rectum: The first case report"],"prefix":"10.1097","volume":"126","author":[{"given":"Raghad","family":"Samha","sequence":"first","affiliation":[{"name":"Faculty of Medicine, AlBaath University, Homs, Syrian Arab Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hossam Tharwat","family":"Ali","sequence":"additional","affiliation":[{"name":"Qena Faculty of Medicine, South Valley University, Qena, Egypt"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Layal","family":"Msheik","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tia","family":"Khadra","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aamer","family":"Zainab","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Almadina Hospital, Damascus, Syrian Arab Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R3-30-20260508","doi-asserted-by":"crossref","first-page":"490","DOI":"10.1001\/archsurg.133.5.490","article-title":"Intestinal atresia and stenosis: a 25-year experience with 277 cases","volume":"133","author":"Dalla Vecchia","year":"1998","journal-title":"Arch. Surg."},{"key":"R4-30-20260508","doi-asserted-by":"crossref","first-page":"671","DOI":"10.1007\/BF02762182","article-title":"Intestinal atresia","volume":"67","author":"Prasad","year":"2000","journal-title":"Indian J. Pediatr."},{"key":"R5-30-20260508","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1007\/BF01658697","article-title":"Diagnosis and treatment of jejunoileal atresia","volume":"17","author":"Touloukian","year":"1993","journal-title":"World J. Surg."},{"issue":"5","key":"R6-30-20260508","doi-asserted-by":"crossref","first-page":"1136","DOI":"10.1097\/JS9.0000000000000373","article-title":"The SCARE 2023 guideline: updating consensus surgical CAse REport (SCARE) guidelines","volume":"109","author":"Sohrabi","year":"2023","journal-title":"Int J Surg Lond Engl."},{"key":"R7-30-20260508","doi-asserted-by":"crossref","first-page":"303","DOI":"10.4103\/jiaps.JIAPS_204_18","article-title":"Total intestinal atresia: revisiting the pathogenesis of congenital Atresias","volume":"24","author":"Aggerwal","year":"2019","journal-title":"J. Indian Assoc. Pediatr. Surg."},{"issue":"24","key":"R9-30-20260508","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1007\/s00383-007-2072-x","article-title":"The scope of emergency paediatric surgery in Tanzania","volume":"1","author":"Mhando","year":"2008","journal-title":"Pediatr. Surg. Int."},{"key":"R10-30-20260508","article-title":"Hereditary multiple intestinal atresia: a case report and review of the literature","volume":"14","author":"Al-Zaiem","year":"2022","journal-title":"Cureus"},{"key":"R11-30-20260508","doi-asserted-by":"crossref","first-page":"849","DOI":"10.1007\/BF00311654","article-title":"Congenital multiple intestinal atresia successfully treated with multiple anastomoses in a premature neonate: report of a case","volume":"26","author":"Hasegawa","year":"1996","journal-title":"Surg. Today"},{"issue":"9","key":"R12-30-20260508","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1186\/s40792-023-01728-2","article-title":"Tubular intestinal duplication extending from the stomach to the ileum associated with multiple intestinal atresia and situs inversus: a case report","volume":"9","author":"Higashidate","year":"2023","journal-title":"Surg Case Rep."},{"issue":"9","key":"R13-30-20260508","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1186\/s40792-023-01761-1","article-title":"Challenging management of a baby with congenital multiple intestinal atresia, trisomy 18 and extremely low birth weight: a case report","volume":"13","author":"Okamoto","year":"2023","journal-title":"Surg Case Rep."},{"key":"R14-30-20260508","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1055\/s-2008-1071133","article-title":"al-Wafi a, Lari J. Gastroschisis and total intestinal atresia","volume":"8","author":"Morris-Stiff","year":"1998","journal-title":"Eur. J. Pediatr. Surg."},{"key":"R17-30-20260508","doi-asserted-by":"crossref","first-page":"103","DOI":"10.4103\/2249-4847.116413","article-title":"Near Total Jejuno-Ileal atresia: a management challenge","volume":"2","author":"Sham","year":"2013","journal-title":"J Clin Neonatol."}],"container-title":["International Journal of Surgery Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261224014494?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261224014494?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.lww.com\/10.1016\/j.ijscr.2024.110668","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,5,8]],"date-time":"2026-05-08T22:00:54Z","timestamp":1778277654000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/10.1016\/j.ijscr.2024.110668"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,1]]},"references-count":12,"journal-issue":{"issue":"C","published-print":{"date-parts":[[2025]]}},"URL":"https:\/\/doi.org\/10.1016\/j.ijscr.2024.110668","relation":{},"ISSN":["2210-2612"],"issn-type":[{"value":"2210-2612","type":"print"}],"subject":[],"published":{"date-parts":[[2025,1]]},"assertion":[{"value":"2024-09-27","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2024-11-25","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}