Meconium peritonitis in stillbirths.

Pediatr Pathol

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115.

Published: June 1989

AI Article Synopsis

  • Meconium peritonitis is a rare condition caused by bowel perforation during fetal development, typically identified through autopsy.
  • The study involved three fetuses, showing signs of meconium peritonitis, with two potentially affected by fetal hypoxia and one exhibiting hydropic changes and abdominal calcifications.
  • Autopsy findings included meconium in the peritoneal cavity and calcified nodules, indicating that meconium peritonitis could be a sign of prior bowel perforation and might be linked to hypoxia during pregnancy.

Article Abstract

Meconium peritonitis is a sterile, chemical peritonitis resulting from perforation of the bowel in perinatal life. In stillbirths meconium peritonitis is extremely rare. We report the autopsy findings in three fetuses ranging from 21-39 weeks gestation in which meconium peritonitis was identified. Maternal history in two cases was suggestive of possible fetal hypoxia. No family history of cystic fibrosis was discerned. One fetus was hydropic and abdominal calcifications were noted on postmortem radiograph. Gross evidence of meconium in the peritoneal cavity, visceral adhesions, and serosal nodules were noted in two fetuses. Nodules of calcified meconium seen by microscopy were the only clues to diagnosis in the third fetus. The discovery of meconium peritonitis at autopsy may be the only residual evidence of antecedent bowel perforation. We suggest that intrauterine hypoxia may play a role in the development of meconium peritonitis in some cases.

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Source
http://dx.doi.org/10.3109/15513818809022318DOI Listing

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