Jejunostomy for enteral trophic feeding in the management of apple-peel intestinal atresia

2021 ◽  
Vol 10 (2) ◽  
pp. 127
Author(s):  
NatalieIsabel Garcia Smith ◽  
CarmenJovani Casano ◽  
BeatrizPemartin Comella ◽  
MartaOlivares Muñoz
Author(s):  
Kiyoshi Imaizumi ◽  
Junko Kimura ◽  
Mitsuo Masuno ◽  
Yoshikazu Kuroki ◽  
Toshiji Nishi

2019 ◽  
Vol 49 ◽  
pp. 101293
Author(s):  
Jalles Filipa ◽  
Morgado Mariana ◽  
Janeiro Marta ◽  
Gonçalves Miroslava

2011 ◽  
Vol 31 (3) ◽  
pp. 227-234 ◽  
Author(s):  
RA Akinola ◽  
RL Osuoji

Background: Although apple peel intestinal atresia is rare and is associated with a high mortality and morbidity, there is a dearth of its report in African literature. This study reviews four of the cases seen in a state teaching hospital in Lagos, considering the radiographic findings, surgical management and outcome. A brief review of literature is also undertaken. Aims and Objectives: To correle the plain radiographic findings with the surgical findings of neonates gathered over a six year period and to evaluate their surgical management, hoping to further help improve management of such neonates’ in future in resource limited regions such as ours. Methodology: It was a retrospective case series of four neonates who were brought in over a period of six years and operated after an initial plain abdominal X-ray. They were done as emergency cases, consent was obtained from their parents and the study was approved by the research and ethics committee. Operative findings were subsequently correlated with their radiographic findings and the surgical outcomes and follow up were documented. Conclusion: This study revealed that “the triple bubble sign” is a common radiographic finding in Apple Peel deformities, as well as gangrene of the jejunum and ileum at surgery. Key words: Apple peel atresia; Jejunoileal atresia; Plain Abdominal Radiography; Parenteral nutrition; Short Bowel Syndrome. DOI: http://dx.doi.org/10.3126/jnps.v31i3.5037 J Nep Paedtr Soc 2011;31(3): 227-234  


2020 ◽  
Author(s):  
Gianluca Caridi ◽  
Francesca Lugani ◽  
Margherita Lerone ◽  
Maria Teresa Divizia ◽  
Gian Marco Ghiggeri ◽  
...  

Abstract Strømme syndrome is a rare autosomal recessive congenital disorder involving multiple systems. Centromeric protein F (CENPF) is the causative gene of the disease, and variants are usually linked to lethal outcomes either during the foetal stage or in early life. We present a young adult with a genetic diagnosis of Strømme syndrome who—in addition to classic microcephalia, microphthalmia and intestinal atresia (apple peel-type)—experienced slow and unexpected evolution to end-stage renal disease (ESRD). In conclusion, Strømme syndrome is a complex multiorgan disease that needs multidisciplinary clinical management, and potential evolution to ESRD should be taken into account.


2013 ◽  
Vol 48 (6) ◽  
pp. e5-e7 ◽  
Author(s):  
Luciano Silveira Onofre ◽  
Renato Frota de Albuquerque Maranhão ◽  
Elaine Cristina Soares Martins ◽  
Camila Girardi Fachin ◽  
Jose Luiz Martins

Sign in / Sign up

Export Citation Format

Share Document