Meconial peritonitis in a rare association of partial ileal apple-peel atresia with small abdominal wall defect

Submitted: 13 November 2014
Accepted: 13 November 2014
Published: 30 June 2014
Abstract Views: 1884
PDF: 2296
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

Intestinal atresia type III B (apple peel) and gastroschisis are both congenital malformations who require early surgical correction in neonatal age. Their association is very rare. We present the case of a full term infant with partial apple peel ileal atresia and a small defect of the anterior abdominal wall, complicated by in utero intestinal perforation and subsequent meconial peritonitis. We observed a partial atresia of small intestine, with involvement of terminal ileus savings of jejunum and a large part of the proximal ileum, small anterior abdominal wall defect with herniation of few bowel loops, intestinal malrotation. Paralytic ileus and infections are the main causes of morbidity and mortality at neonatal age. In our case, in spite of the mild phenotype, prognosis has been complicated by the onset of functional bowel obstruction, caused by chemical peritonitis resulting from contact with either amniotic fluid and meconium.

Dimensions

Altmetric

PlumX Metrics

Downloads

Download data is not yet available.

Citations

How to Cite

Insinga, V., Pensabene, M., Giuffrè, M., Busè, M., Cimador, M., Corsello, G., & Siracusa, F. (2014). Meconial peritonitis in a rare association of partial ileal apple-peel atresia with small abdominal wall defect. La Pediatria Medica E Chirurgica, 36(3). https://doi.org/10.4081/pmc.2014.8

Similar Articles

<< < 1 2 3 4 5 6 7 8 9 10 > >> 

You may also start an advanced similarity search for this article.