Meconium peritonitis

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Meconium peritonitis
Classification and external resources
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ICD-10 P78.0
ICD-9-CM 777.6
Patient UK Meconium peritonitis
[[[d:Lua error in Module:Wikidata at line 863: attempt to index field 'wikibase' (a nil value).|edit on Wikidata]]]
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.

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.

References

  1. Tseng JJ, Chou MM, Ho ES (June 2003). "Meconium peritonitis in utero: prenatal sonographic findings and clinical implications". J Chin Med Assoc. 66 (6): 355–9. PMID 12889504.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  2. Lua error in Module:Citation/CS1/Identifiers at line 47: attempt to index field 'wikibase' (a nil value).

External links