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Pancytopenia in an infant associated with sulfamethoxazole-trimethoprim therapy
The Journal of Pediatrics
|March 1, 1976
Insights
Sulfamethoxazole-trimethoprim caused pancytopenia in an infant. Bone marrow showed prominent plasma cells and histiocytes, atypical for aplastic anemia.
Area of Science:
- Pediatric Hematology
- Pharmacology
- Toxicology
Background:
- Pancytopenia is a serious condition characterized by a deficiency in all three major blood cell types.
- Sulfamethoxazole-trimethoprim is a commonly prescribed antibiotic combination.
- Aplastic anemia typically presents with a hypocellular bone marrow.
Observation:
- A seven-month-old infant developed pancytopenia.
- The condition was linked to sulfamethoxazole-trimethoprim treatment.
- Initial bone marrow examination revealed prominent plasma cells and histiocytes.
Findings:
- The infant's bone marrow morphology was distinct from the usual presentation of aplastic anemia.
- This case suggests a potential adverse drug reaction to sulfamethoxazole-trimethoprim.
- The prominent plasma cells and histiocytes represent an unusual bone marrow finding in drug-induced pancytopenia.
Implications:
- This case highlights the importance of considering drug-induced pancytopenia in infants presenting with low blood counts.
- Clinicians should be aware of the atypical bone marrow findings associated with sulfamethoxazole-trimethoprim.
- Further investigation may be warranted to understand the mechanism of this adverse reaction.
Abstract:
Pancytopenia in a seven-month-old baby is described and attributed to sulfamethoxazole-trimethoprim therapy. Plasma cells and histiocytes were prominent in the initial bone marrow examination and quite unlike the fatty hypocellular marrow usually seen in aplastic anemia.