Publication:
Omphalocele, Exstrophy of Cloaca, Imperforate Anus, and Spinal Defects Complex: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorSingh, Suraj
dc.contributor.authorKayastha, Anuj
dc.contributor.authorThapa, Anupama
dc.contributor.authorThapa, Bijay
dc.contributor.authorDahal, Sulochana
dc.date.accessioned2025-09-26T07:37:04Z
dc.date.available2025-09-26T07:37:04Z
dc.date.issued2023
dc.descriptionSuraj Singh Department of Pediatrics Surgery, Kanti Children’s Hospital, Maharajgunj, Kathmandu, Nepal Anuj Kayastha Department of Pediatrics Surgery, Kanti Children’s Hospital, Maharajgunj, Kathmandu, Nepal Anupama Thapa Department of Pediatrics Surgery, Kanti Children’s Hospital, Maharajgunj, Kathmandu, Nepal Bijay Thapa Department of Pediatrics Surgery, Kanti Children’s Hospital, Maharajgunj, Kathmandu, Nepal Sulochana Dahal Department of Pediatrics Surgery, Kanti Children’s Hospital, Maharajgunj, Kathmandu, Nepal https://orcid.org/0000-0002-4389-0168
dc.description.abstractAbstract Omphalocele, exstrophy of cloaca, imperforate anus, and spinal defects complex is a rare malformation complex that includes omphalocele, cloacal exstrophy, imperforate anus and spinal defects with the incidence of 1 in 200,000 to 400,000 pregnancies and is even rarer in twin gestation. The etiology of this complex is still unclear. Most cases are sporadic. Prenatal screening must be done for diagnosis and appropriate multidisciplinary management of cases. In severe cases, termination of pregnancy is considered. We present a 4-day first twin child with underdeveloped ambiguous genitalia delivered via emergency lower section cesarean section at 32+3 weeks of gestation with giant liver containing omphalocele, cloacal exstrophy, imperforate anus and meningocele with severe pulmonary artery hypertension and non-visualization of right kidney and ureter, absence of uterus, fallopian tubes and right ovary. Separation and repair of the cecum and bladder were done. The ladd procedure was performed. Ileostomy was created and single-stage repair of the abdominal wall was done.
dc.identifierhttps://doi.org/10.31729/jnma.8048
dc.identifier.urihttps://hdl.handle.net/20.500.14572/2398
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.subjectAnorectal malformations
dc.subjectBladder exstrophy
dc.subjectCase reports
dc.subjectNeural tube defects
dc.subjectUmbilicus
dc.subject375
dc.titleOmphalocele, Exstrophy of Cloaca, Imperforate Anus, and Spinal Defects Complex: A Case Report
dc.typeOther
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage378
oaire.citation.startPage375
relation.isJournalIssueOfPublicationcb29f96c-a94f-4864-95b6-9f7f36256766
relation.isJournalIssueOfPublication.latestForDiscoverycb29f96c-a94f-4864-95b6-9f7f36256766
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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