Meconium peritonitis
From Infogalactic: the planetary knowledge core
| Meconium peritonitis | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | P78.0 |
| ICD-9-CM | 777.6 |
| Patient UK | Meconium peritonitis |
File:Mekoniumzyste bei terminaler Ileumatresie - Roe 001.jpg
X-ray of a newborn with meconium pseudocyst resulting from bowel perforation. In this case the cause was atresia of the terminal ileum. There is a fine rim of calcification surrounding the big pseudocyst which shifts the other intestinal structures outwards.
Meconium peritonitis refers to rupture of the bowel prior to birth, resulting in fetal stool (meconium) escaping into the surrounding space (peritoneum) leading to inflammation (peritonitis). Despite the bowel rupture, many infants born after meconium peritonitis in utero have normal bowels and have no further issues.
Infants with cystic fibrosis are at increased risk for meconium peritonitis.
Contents
Diagnosis
Twenty percent of infants born with meconium peritonitis will have vomiting and dilated bowels on x-rays which necessitates surgery.
Meconium peritonitis is sometimes diagnosed on prenatal ultrasound[1] where it appears as calcifications[2] within the peritoneum.
History
Meconium peritonitis was first described in 1838 by Carl von Rokitansky.
