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Cerebral infarction as the first presentation of tuberculosis in an infant: a case report
Farid Radmanesh1, Farideh Nejat, Mostafa El Khashab
1Department of Neurosurgery, Children's Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Tuberculosis in a child presented unusually with stroke-like symptoms and hydrocephalus. Diagnosis was confirmed via peritoneal biopsy and cerebrospinal fluid analysis, leading to successful treatment with antitubercular therapy.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Pediatric stroke and hydrocephalus require thorough etiological investigation.
- Tuberculosis (TB) can present with diverse neurological manifestations, often including constitutional symptoms.
Observation:
- A child presented with acute hemiparesis and seizures, initially suspected as an ischemic event.
- Progressive hydrocephalus necessitated ventriculoperitoneal shunting, which later became infected.
- Peritoneal thickening and granulomatous reaction on biopsy, alongside positive cerebrospinal fluid PCR, confirmed disseminated tuberculosis.
Findings:
- The case highlights an atypical presentation of tuberculosis (TB) in a child, manifesting initially as cerebral infarction and hydrocephalus.
- Cerebrospinal fluid (CSF) polymerase chain reaction (PCR) and peritoneal biopsy were crucial for diagnosing TB.
- The patient showed significant recovery after initiating antitubercular therapy and shunt revision.
Implications:
- This case underscores the importance of considering disseminated tuberculosis in pediatric patients with unexplained neurological deficits and hydrocephalus, even without typical systemic symptoms.
- It emphasizes the diagnostic utility of peritoneal biopsy and CSF PCR in complex cases.
- Early diagnosis and appropriate antitubercular treatment are vital for favorable neurological outcomes in such presentations.
Abstract:
The case of a child admitted to hospital with acute onset of hemiparesis and seizure is presented. Extensive evaluation of an acute ischemic event in the form of a brain infarct found on brain magnetic resonance imaging was inconclusive. Two months later, the patient was referred with severe hydrocephalus, which was managed with ventriculoperitoneal shunting in the presence of normal ventricular cerebrospinal fluid. The shunt was complicated by distal end infection. During the insertion of a second shunt, and after 3 months of antibiotic therapy, peritoneal thickening was found. Peritoneal biopsy showed evidence of a granulomatous reaction. This finding, along with positive polymerase chain reaction of the cerebrospinal fluid, confirmed tuberculosis. The patient recovered from most of his symptoms after antituberculous therapy, and a new ventriculoperitoneal shunt was inserted. This is a very peculiar presentation of tuberculosis that began with a cerebral infarction due to vasculopathy and hydrocephalus without any constitutional symptoms, and was later confirmed by peritoneal pathology.
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