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Hyper-reactive malarial splenomegaly: rare cause of pyrexia of unknown origin
1Department of Pediatrics, University College of Medical Sciences and Guru Teg Bahadur Hospital, Delhi, India.
Insights
Hyper-reactive malarial splenomegaly (HMS), also known as Tropical splenomegaly syndrome (TSS), is typically seen in young adults. This report details a rare case of HMS in a three-year-old child presenting with prolonged fever and enlarged liver and spleen.
Area of Science:
- Tropical medicine
- Pediatric infectious diseases
- Clinical case reports
Background:
- Hyper-reactive malarial splenomegaly (HMS), or Tropical splenomegaly syndrome (TSS), is a clinical condition associated with high malaria transmission zones.
- HMS typically affects young adults and is characterized by significant splenomegaly and abdominal discomfort, with fever being an infrequent symptom.
Observation:
- A three-year-old child presented with pyrexia of unknown origin and hepatosplenomegaly.
- This presentation is unusual as HMS is rarely diagnosed in children under eight years of age.
Findings:
- The child was diagnosed with Hyper-reactive malarial splenomegaly (HMS).
- This case highlights the potential for HMS to occur in younger pediatric populations, challenging the typical age demographic.
Implications:
- This case expands the known age range for Hyper-reactive malarial splenomegaly (HMS) diagnosis.
- It suggests that clinicians should consider HMS in the differential diagnosis of pyrexia of unknown origin with hepatosplenomegaly in young children from endemic areas.
- Further research may be needed to understand the specific factors contributing to early-onset HMS.
Abstract:
Hyper-reactive malarial splenomegaly (HMS) or Tropical splenomegaly syndrome(TSS), occurs in areas of high transmission of malaria. These children usually presents with gross splenomegaly and abdominal discomfort, while fever is not the usual manifestation in majority of them. It is a disease of young adults and rarely reported below 8 years of age. Here it is reported a three-year-old child who presented as pyrexia of unknown origin with hepatosplenomegaly, diagnosed as HMS.
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