Literature DB >> 4090747

Congenital short small bowel with malrotation in a neonate.

N Iwai, J Yanagihara, T Tsuto, H Taniguchi, T Takahashi.   

Abstract

A 1-day-old male infant with congenital short small bowel was transferred to our hospital because of bilious vomiting and abdominal distension. An exploratory laparotomy performed at the age of 8 days revealed malrotation without any volvulus or stenosis of the small intestine, which was 45 cm long. There were no other anomalies except absence of the appendix. Postoperative nutritional support was by intravenous hyperalimentation and administration of elemental diet. However, parenteral nutrition was discontinued because of hyperbilirubinaemia. The patient died from marked emaciation at 2 months of age despite the administration of elemental diet. Therefore, careful total parenteral nutrition is the only management for successful therapy until the child's intestinal absorptive function develops.

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Year:  1985        PMID: 4090747     DOI: 10.1055/s-2008-1059753

Source DB:  PubMed          Journal:  Z Kinderchir        ISSN: 0174-3082


  3 in total

1.  Congenital short-gut syndrome.

Authors:  Gauravi Sabharwal; Peter J Strouse; Saleem Islam; Najeeb Zoubi
Journal:  Pediatr Radiol       Date:  2003-12-16

2.  First Report of Congenital Short Bowel Syndrome in an Iranian Patient Caused by a Mutation in the CLMP Gene.

Authors:  Jalal Gharesouran; Behnaz Salek Esfahani; Saeed Farajzadeh Valilou; Mohsen Moradi; Mir Hadi Mousavi; Maryam Rezazadeh
Journal:  J Pediatr Genet       Date:  2018-10-26

Review 3.  Congenital short bowel syndrome: a case report and review of the literature.

Authors:  Mohammed Hasosah; Daniel A Lemberg; Eric Skarsgard; Richard Schreiber
Journal:  Can J Gastroenterol       Date:  2008-01       Impact factor: 3.522

  3 in total

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