AI Article Synopsis
- Kasabach-Merritt syndrome is a rare condition that requires quick identification and treatment to prevent severe bleeding and reduce the risk of death.
- The authors describe a case involving a Cambodian newborn who showed symptoms like anemia and jaundice on Day 5 but was not diagnosed with the syndrome until it was too late.
- The delay in recognizing and addressing the mass led to the infant's unfortunate death.
Article Abstract
Key Clinical Message: Kasabach-Merritt syndrome is a rare disease. Early recognition, timely transfer, and proper management are crucial in reducing bleeding complication and mortality.
Abstract: The authors report a rare case of Kasabach-Merritt syndrome in a Cambodian neonate presenting with anemia and jaundice at Day 5 of life. Since the mass was not recognized at birth, the diagnosis and treatment were delayed, thus leading to demise.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620114 | PMC |
| http://dx.doi.org/10.1002/ccr3.8089 | DOI Listing |
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