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Leprosy: a case series and review.
Joshua D Hartzell1, Michael Zapor, Suzette Peng
1Department of Internal Medicine, Walter Reed Army Medical Center, Washington, DC 20307, USA. joshua.hartzell@na.amedd.army.mil
Southern Medical Journal
|January 14, 2005
Summary
Hansen disease (leprosy) is rare in the US but can affect military personnel from endemic areas. Prompt diagnosis is crucial to prevent disability, as cases may be misdiagnosed initially.
Area of Science:
- Medical Microbiology
- Infectious Diseases
- Dermatology
Background:
- Hansen disease, caused by Mycobacterium leprae, is historically known as leprosy.
- While rare in the US, it remains endemic in certain populations and can manifest years post-infection.
- US military personnel from endemic countries may be at risk.
Purpose of the Study:
- To highlight the diagnostic challenges and delays in Hansen disease cases within the US military.
- To emphasize the importance of early recognition and treatment of Hansen disease.
- To discuss the clinical presentation, diagnosis, classification, and treatment of Hansen disease.
Main Methods:
- Case series review of three US soldiers diagnosed with Hansen disease at Walter Reed Army Medical Center.
- Analysis of diagnostic timelines and initial misdiagnoses.
- Review of current literature on Hansen disease management.
Main Results:
- The mean time to diagnosis for the three soldiers was 8 months (range: 2-18 months).
- All three patients were initially misdiagnosed with other skin conditions, such as infections or contact dermatitis.
- Delayed diagnosis underscores challenges in recognizing Hansen disease in non-endemic settings.
Conclusions:
- Hansen disease requires a high index of suspicion, especially in at-risk populations like US military personnel from endemic regions.
- Prompt diagnosis and treatment are essential to prevent irreversible physical deformities and disabilities.
- Further education on Hansen disease presentation is needed for healthcare providers to avoid diagnostic delays.