Pneumoperitoneum in in-vitro Conceived Quadruplet Neonate: Rare Manifestation of Hirschsprung's Disease--Report of a Case
Language English Country Czech Republic Media print
Document type Case Reports, Journal Article
PubMed
26960828
DOI
10.14712/18059694.2016.7
PII: am_2015058040144
Knihovny.cz E-resources
- Keywords
- Hirschsprung disease, In vitro fertilization, Pneumoperitoneum, quadruplets,
- MeSH
- Quadruplets * MeSH
- Fertilization in Vitro MeSH
- Hirschsprung Disease complications diagnosis surgery MeSH
- Humans MeSH
- Infant, Premature MeSH
- Infant, Newborn MeSH
- Pneumoperitoneum diagnosis etiology surgery MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
INTRODUCTION: Hirschsprung's disease is a congenital colonic aganglionosis, usually presented as inability or difficulty in passing of meconium, chronic and persistent obstipation, maleficent feeding, vomiting, distension and lethargy. CASE PRESENTATION: We presented a case of an in-vitro conceived quadruplet premature neonate who presented with pneumoperitoneum caused by transverse colon spontaneous perforation and microcolon appearance of distal bowel, treated by resection and temporary colostomy turns to be a rare manifestation of Hirschsprung's disease. CONCLUSION: Assisted reproductive technologies increases chances for multiple pregnancies and may increase chance for major congenital anomalies. Rare manifestation of Hirschsprung's disease is spontaneous pneumoperitoneum which remains a surgical emergency. Delay in recognizing and treatment can significantly worsen prognosis. In neonate with intestinal perforation one should consider Hirschsprung's disease.
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