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Published on: October 29, 2014
A 10-month-old with rotavirus gastroenteritis, seizures, anasarca and systemic inflammatory response syndrome and
Sulaiman S Bharwani1, Qudsia Shaukat, Ratna Basak
1Department of Pediatrics, UAE University, Faculty of Medicine and Health Sciences, Al Ain, United Arab Emirates. sulaiman.bharwani@gmail.com
Insights
A 10-month-old infant experienced severe symptoms including seizures and shock after a rotavirus infection. Prompt medical intervention led to a full recovery within 12 days.
Area of Science:
- Pediatrics
- Infectious Diseases
- Gastroenterology
Background:
- Rotavirus is a common cause of gastroenteritis in infants.
- Severe complications can arise, necessitating prompt diagnosis and management.
Observation:
- A 10-month-old infant presented with seizures, vomiting, diarrhea, and fever.
- Initial investigations revealed hyponatremia, leukocytosis, thrombocytosis, hypoalbuminemia, and elevated CRP.
- Stool analysis was positive for rotavirus antigen, with microscopic hematuria and coffee-ground nasogastric aspirate.
Findings:
- The infant developed generalized edema, effusions, shock, and disseminated intravascular coagulopathy (DIC).
- Treatment included fluid/electrolyte correction, albumin infusions, and blood product transfusions.
- The patient recovered fully within 12 days.
Implications:
- This case highlights the potential for severe, systemic complications of rotavirus infection in infants.
- Early recognition and aggressive supportive care are crucial for managing such critical cases.
- Further research into the mechanisms of rotavirus-induced systemic illness may improve treatment strategies.
Abstract:
This report describes a 10-month-old infant who presented with generalised tonic clonic seizures following 2 days of vomiting, diarrhoea and a low-grade fever. The patient was moderately dehydrated and the blood investigations were remarkable for hyponatraemia (126 mEq/l), leukocytosis (19.4 × 10(3)/l (46% lymphocytes)), thrombocytosis (637 × 10(3)/l), hypoalbuminaemia (albumin 1.9 g/dl) and elevated C reactive protein (96 mg/l). Stool was positive for white and red blood cells but the cultures for bacteria were negative. Rotavirus antigen in stool was positive. There was microscopic haematuria without proteinuria and the nasogastric aspirate was coffee ground. Generalised oedema with pleural and peritoneal effusions ensued requiring drainage, correction of fluid and electrolytes imbalance and albumin infusions. Over the next 72 h, the patient descended into shock and disseminated intravascular coagulopathy which required packed red blood cells and fresh frozen plasma transfusions. By day 12 the patient was clinically and biochemically normal.
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