| Literature DB >> 28532916 |
Michael George Zaki Ghali1, Visish M Srinivasan2, Marc J Kim3, Archana Malik4.
Abstract
BACKGROUND: Tuberculous involvement of the spinal cord parenchyma is an exceedingly rare clinical entity; even more so is concurrent intracranial tuberculosis (TB). Spinal intramedullary TB presents with a characteristic subacute myelopathy, with slowly progressive paraplegia, sensory deficits, and/or bowel and bladder dysfunction. Diagnosis is strongly suspected with a clinical history of known TB in conjunction with characteristic findings on magnetic resonance imaging. Management involves multiagent antitubercular chemotherapy without or with operative intervention. CASE DESCRIPTION: We present a case of a 9-month-old boy with a retrospectively recognized history of pulmonary TB presenting with fever and back tenderness found to have lower-extremity hypertonia and clonus. Imaging revealed concurrent intracranial and spinal intramedullary tuberculomas. The patient was treated for hydrocephalus with external ventricular drainage followed by T8-T10 laminectomy, drainage of abscess, and duraplasty. Parietal lobe biopsies proved the tuberculous etiology of intracranial lesions.Entities:
Keywords: CNS; Disseminated tuberculosis; Intramedullary; TB; Tuberculoma; Tuberculosis
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Year: 2017 PMID: 28532916 DOI: 10.1016/j.wneu.2017.05.069
Source DB: PubMed Journal: World Neurosurg ISSN: 1878-8750 Impact factor: 2.104