Multiple organ failure syndrome in the newborn: morphological and immunohistochemical data

J Matern Fetal Neonatal Med. 2012 Oct;25(Suppl 5):68-71. doi: 10.3109/14767058.2012.714643.

Abstract

Multiple organ failure (MOF) syndrome, also known as multiple organ dysfunction syndrome (MODS) represents a common but complex problem in critically ill patients in neonatal intensive care unit (NICU) centers, and a major cause of morbidity and mortality in newborns. MOF is considered the result of an inappropriate generalized inflammatory response of the newborn to a variety of acute insults. This study was aimed at analyzing, at histology, multiple organ pathological changes in two newborns admitted to the NICU center of our University Hospital, who showed a progressive clinical picture of MOF, in order to verify the pathological changes of vascular structures and of endothelial cells in the different organs affected by MOF. All the samples obtained at autopsy for histological examination showed specific organ pathological changes, especially related to modifications in vascular structures and, in particular, in endothelial cells. The most interesting findings were found in the intestinal barrier, in the lower respiratory tract and in the endothelial barrier. The loss of the gut barrier could allow the passage into the blood of microbial factors that could trigger the production of tumor necrosis factor α (TNFα) leading to endothelial damage. Our preliminary study underlines the principal role probably played by intestinal and vascular changes in the origin of MOF in newborns.

MeSH terms

  • Blood Vessels / pathology
  • Cytokines / metabolism
  • Endothelial Cells / pathology
  • Humans
  • Immunohistochemistry
  • Infant, Newborn
  • Intensive Care, Neonatal
  • Intestines / blood supply
  • Intestines / pathology
  • Multiple Organ Failure / etiology
  • Multiple Organ Failure / pathology*
  • Multiple Organ Failure / physiopathology*
  • Respiratory System / blood supply
  • Respiratory System / pathology

Substances

  • Cytokines