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Newly Diagnosed Hemoglobin SC Disease Presenting With Choledocholithiasis With Acute Obstructive Cholangitis: A Case
Daniel T Tran1, Justin J Youn2, Gary Thompson3
1Internal Medicine, Loma Linda University School of Medicine, Loma Linda, USA.
Hemoglobin SC disease (HbSC), often mild, can cause serious complications like acute cholangitis. Early diagnosis of HbSC in high-risk individuals is crucial for timely treatment and improved quality of life.
Area of Science:
- Hematology
- Genetics
Background:
- Sickle cell disease (SCD) encompasses various genetic disorders, including Hemoglobin SS (HbSS) and Hemoglobin SC (HbSC) disease.
- HbSC is typically considered milder than HbSS, often presenting with fewer and less severe complications.
Observation:
- Despite its milder classification, HbSC can be underdiagnosed due to asymptomatic presentation or mild symptoms.
- A case of newly diagnosed HbSC presented with acute cholangitis secondary to choledocholithiasis, a potentially life-threatening condition.
Findings:
- This case highlights that severe, clinically significant complications can arise in individuals with HbSC.
- The presentation of acute cholangitis underscores the potential for serious biliary tract disease in HbSC patients.
Implications:
- Early screening and diagnosis of HbSC in at-risk populations are essential for proactive management.
- Timely intervention may prevent severe complications, reduce healthcare burdens, and enhance the quality of life for HbSC patients.
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