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Coexisting Spinal Intramedullary and Intracranial Tuberculomas in an Immunocompetent Child
Vaishali R Ghane1, Preeti Shanbag1, Ashish Meshram1
1Department of Paediatrics, ESI Post Graduate Institute of Medical Science and Research and ESIC Model Hospital, Andheri, Mumbai, Maharashtra, India.
Journal of Pediatric Neurosciences
|October 26, 2019
Summary
Pediatric neurotuberculosis, though rare, can present as coexisting intramedullary and intracranial tuberculomas. Early diagnosis and treatment with antituberculosis therapy and steroids led to a full recovery in a 5-year-old boy.
Area of Science:
- Neurology
- Infectious Diseases
- Pediatrics
Background:
- Pediatric neurotuberculosis commonly involves tuberculous meningitis and intracranial tuberculomas.
- Intramedullary tuberculomas (IMTs) are rare spinal cord lesions.
- The coexistence of IMT and intracranial tuberculoma is exceptionally uncommon.
Observation:
- A 5-year-old boy presented with fever, progressive lower limb weakness, urinary retention, and constipation.
- Neurological examination indicated compressive myelopathy.
- Spinal MRI revealed an intramedullary tuberculoma at D4-D5 with edema; brain MRI showed a right frontal tuberculoma.
Findings:
- The case highlights an extremely rare instance of coexisting intramedullary and intracranial tuberculoma in a child.
- Magnetic resonance imaging was crucial for diagnosing both spinal and intracranial lesions.
- Successful management involved a combination of antituberculosis therapy and corticosteroids.
Implications:
- This case underscores the importance of considering disseminated neurotuberculosis even in rare presentations.
- Prompt diagnosis and multimodal treatment can lead to favorable neurological outcomes in pediatric patients.
- Further research into the pathogenesis and optimal management of coexisting spinal and intracranial tuberculomas is warranted.
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