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Updated: Jul 5, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Death due to sickle cell crisis: a case report
Teaghan Koster1, Elizabeth Boyer2, David J Clutterbuck3,4,5
1Department of Pathology and Molecular Medicine, Queen's University, 76 Stuart St, Kingston, ON, K7L 2V7, Canada. t.koster@queensu.ca.
Sickle cell disease (SCD) presents distinct postmortem findings on imaging and examination. Forensic pathologists can identify SCD by combining these with microscopic evidence, aiding in cause of death determination.
Area of Science:
- Forensic Pathology
- Hematology
- Medical Imaging
Background:
- Sickle cell disease (SCD) is a prevalent global hemoglobinopathy.
- SCD causes characteristic acute and chronic changes detectable postmortem.
- Forensic pathology literature infrequently details SCD's postmortem manifestations.
Observation:
- This case highlights classic acute and chronic SCD features on postmortem CT (PMCT), gross, and microscopic examination.
- Diagnostic imaging and macroscopic findings alone are not specific for SCD.
- Microscopic evidence, including sickled erythrocytes and Gamna-Gandy bodies, is crucial for SCD identification.
Findings:
- Postmortem CT, macroscopic, and microscopic findings in SCD are presented.
- The study details the pathophysiology of sudden death in individuals with SCD.
- Potential challenges in attributing cause of death in SCD cases are discussed.
Implications:
- Recognizing SCD's postmortem features improves diagnostic accuracy in forensic investigations.
- This case underscores the importance of integrating imaging and microscopic findings.
- Understanding SCD pathophysiology aids in determining cause of death in unexpected fatalities.
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