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Published on: September 5, 2017
Congenital tuberculosis: a case report
Liana Consuelo Santana Vilarinho1
1Federal University of Bahia, Salvador, BA, Brazil. lianavilarinho@uol.com.br
Insights
Congenital tuberculosis in infants is rare and challenging to treat. This case highlights successful management through adjusted anti-tuberculosis drug dosages, improving infant outcomes.
Area of Science:
- Pediatrics
- Infectious Diseases
- Public Health
Background:
- Congenital tuberculosis (Mycobacterium tuberculosis infection) is a rare but severe condition.
- It presents significant diagnostic and therapeutic challenges, particularly in neonates and infants.
- Maternal tuberculosis is a primary risk factor for congenital transmission.
Observation:
- A two-month-old infant presented with fever, dyspnea, and a diffuse micronodular pattern on chest X-ray, with a history of maternal tuberculosis.
- Initial triple-drug anti-tuberculosis therapy led to jaundice and elevated liver enzymes, indicating drug intolerance.
- Alternative treatment regimens failed to resolve the infant's persistent fever.
Findings:
- Increasing the dosage of isoniazid (INH) and rifampicin (RMP) in the anti-tuberculosis regimen resulted in the resolution of fever.
- The infant was successfully treated and cured of congenital tuberculosis.
- This case underscores the complexities in managing congenital tuberculosis, especially concerning drug tolerance and efficacy.
Implications:
- Highlights the need for careful monitoring and individualized treatment adjustments in congenital tuberculosis.
- Suggests that optimizing anti-tuberculosis drug dosages may be crucial for successful treatment in infants with intolerance.
- Emphasizes the importance of developing specific clinical protocols to address the diagnostic and therapeutic difficulties of congenital tuberculosis.
Abstract:
Congenital tuberculosis is an unusual and severe clinical pattern of tuberculosis presentation of Mycobacterium tuberculosis infection. Furthermore, it usually has a difficult treatment. We report a two-month-old male infant who presented with fever, dyspnea and a diffuse micronodular pattern at x-ray; mother with severe tuberculosis. Treatment with the triple drug regimen was initiated, but the child developed jaundice and an increase in liver enzymes on various occasions during treatment. A regimen specifically developed for cases of intolerance was initiated but there was no improvement in hyperthermia. Finally, the dose of INH and RMP was increased, the fever receded and the child was cured. This case remarks difficulties on diagnosis and therapeutic management about this important severe disease in public health, and alert for development of protocols that foresee these difficulties.
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