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Childhood borderline lepromatous leprosy: a case report
Grace Dumamawarni Hutahaean1, Martin Susanto1, Tiopan Napitupulu1
1Faculty of Medicine, University of Sumatera Utara, Medan, Indonesia.
Insights
Childhood leprosy indicates control program failures, with new cases emerging despite elimination declarations. Early diagnosis and treatment are vital for preventing lifelong disability and transmission.
Area of Science:
- Medical Science
- Public Health
- Infectious Diseases
Background:
- Childhood leprosy signifies failures in disease control and transmission programs.
- Despite being declared eliminated, new cases persist in endemic regions.
- Children are highly vulnerable due to developing immunity and household exposure.
Observation:
- A 9-year-old Indonesian male presented with borderline lepromatous leprosy.
- Symptoms included stiff fingers and hypopigmented patches, with a family history of leprosy.
- Acid-fast bacilli were identified in tissue scrapings.
Findings:
- The patient received 12 months of multidrug therapy for multibacillary leprosy.
- Post-treatment observation showed no new skin lesions.
- Existing hypopigmented patches showed signs of fading.
Implications:
- Early diagnosis and treatment are crucial for preventing leprosy-related disability.
- Effective treatment reduces the physical, psychosocial, and economic impact of the disease.
- Continued vigilance is necessary for leprosy control and prevention.
Background:
Leprosy in children is a strong indicator of the recent failure of leprosy control and disease transmission programs. For twenty-two years, leprosy has been declared `eliminated as a public health hazard,` yet new cases continue to emerge in endemic areas. The new case detection rate among the child population was recorded at 4.4 per million children. Because of their underdeveloped or neonatal immunity and exposure to intrafamilial contacts, children tend to be the most vulnerable population.
Case:
We present a case of the borderline lepromatous type of leprosy in a 9-year-old Indonesian male patient with the chief complaint of three stiff fingers on his left hand that began four years ago and hypopigmented patches on the back and buttocks that began five years ago. In this case, there was a history of leprosy in his mother`s sister, who had died. Leprosy in the patient was suspected of possibly being transmitted from his mother`s sister who had intense contact with the patient. The results of bacteriological examination with Ziehl- Neelsen staining of tissue scrapings found acid-fast bacilli. He was treated with a multibacillary multidrug regimen for 12 months. Periodical observations after the patient received the treatment revealed no new spots on the patient`s skin, some of the previous hypopigmented patches seemed to fade, especially those on the back.
Conclusions:
In the absence of an effective vaccine, early diagnosis and treatment are critical in preventing disability and deformity and reducing the physical, psychosocial, and economic burden of the disease.
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