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Published on: August 25, 2012
Postoperative hyperthermia-induced multiple organ failure in a child with Down syndrome: a case report
Keiichi Koizumi1,2, Fuminori Numano2, Tomoko Tandou3,4
1Department of Pediatrics, Fujiyoshida Municipal Hospital, Yamanashi, Japan.
Insights
Psychological stress may trigger severe hyperthermia in children with Down syndrome. This rare case highlights the link between stress, hyperthermia, and multiple organ failure in the perioperative period.
Area of Science:
- Pediatric critical care medicine
- Immunology
- Genetics
Background:
- Psychological stress is a known trigger for hyperthermia.
- Persistent hyperthermia can lead to systemic inflammation and organ damage.
- Down syndrome is associated with immune system dysregulation.
Observation:
- A 10-month-old boy with Down syndrome experienced recurrent noninfectious fevers post-procedure.
- Postoperative hyperthermia reached 42°C, refractory to treatment.
- The patient developed hypercytokinemia and multiple organ failure.
Findings:
- Elevated serum interleukin-6 and interleukin-10 levels indicated severe hypercytokinemia.
- The patient exhibited hypoxemia, acidosis, liver dysfunction, coagulopathy, and pancytopenia.
- Infectious and non-infectious causes of fever were ruled out.
Implications:
- This case suggests psychological stress may precipitate severe hyperthermia in susceptible children.
- Combined with Down syndrome-related immune issues, stress-induced hyperthermia can be fatal.
- Understanding this pathway is crucial for managing perioperative hyperthermia in children.
Background:
Psychological stress has been reported to cause hyperthermia. Persistent excessive hyperthermia can, in turn, cause hypercytokinemia and organ damage. We report a case of postoperative severe hyperthermia leading to a systemic inflammatory response and multiple organ failure in a child with Down syndrome.
Case Presentation:
A 10-month-old native Japanese boy with Down syndrome and Hirschsprung's disease is described. Newborn screening showed congenital hypothyroidism and a ventricular septal defect, but these conditions were stable upon administration of levothyroxine and furosemide. His development was equivalent to that of a child with Down syndrome. He developed a noninfectious high fever twice after preoperative preparations at age 8 months and again at 9 months. He was readmitted to hospital at age 10 months to undergo the Soave procedure to correct Hirschsprung's disease. However, he contracted a fever immediately after the surgical procedure. Hyperthermia (42 °C) was refractory to acetaminophen treatment and deteriorated to multiple organ failure due to hypercytokinemia, with increased serum levels of interleukin-6 (44.6 pg/mL) and interleukin-10 (1010 pg/mL). He died on postoperative day 2 with hypoxemia, respiratory/metabolic acidosis, increased serum levels of transaminases, reduced coagulation, and pancytopenia. Various infectious and noninfectious causes of hyperthermia could not be identified clearly by culture or blood tests.
Conclusions:
We speculated that the proximate cause of the fever was psychological stress, because he suffered repeated episodes of hyperthermia after the invasive procedure. Hyperthermia, together with the immune-system disorders associated with Down syndrome, may have induced hypercytokinemia and multiple organ failure. This rare case of noninfectious postoperative hyperthermia leading to multiple organ failure may help to shed further light on the currently unclear pathogenic mechanism of hyperthermia and associated multiple organ failure during the perioperative period in children.
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