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DOI 10.1016/j.ejpn.2012.04.005

Медицинская библиотека · European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society · 2012

Neurological manifestations of TB-IRIS: a report of 4 children.

van Toorn Ronald, Rabie Helena, Dramowski Angela, Schoeman Johan F

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Аннотация

INTRODUCTION

Tuberculosis-associated immune reconstitution inflammatory syndrome (TB-IRIS) is a potentially life-threatening complication in HIV infected children with tuberculosis (TB) of the central nervous system. HIV-associated TB-IRIS has not been previously described in children with neurotuberculosis.

OBJECTIVE

To describe the neurological and neuro-radiological features of 4 consecutive cases of TB-IRIS in children with neurotuberculosis and to discuss possible management strategies.

RESULTS

Three patients treated for tuberculosis of the central nervous system experienced paradoxical worsening of neurological symptoms when combination antiretroviral therapy (cART) was initiated. Intracranial tuberculomas were unmasked in the 4th patient. All patients developed new neurological signs within 10 days of cART initiation. Neurological symptoms and signs included headache, seizures, meningeal irritation, decreased level of consciousness, ataxia and focal motor deficit. Interventions included the temporary discontinuation of cART and the use of corticosteroids in all patients. Three patients received thalidomide and 1 chloroquine and mycophenolate mofetil. One patient died and the others experienced prolonged hospitalization.

CONCLUSION

TB-IRIS should be considered when new neurological signs develop shortly after initiation of cART in children. There is little data to guide the timing of initiation of cART and the management of complications in children.

Для цитирования: van Toorn Ronald, Rabie Helena, Dramowski Angela, Schoeman Johan F. Neurological manifestations of TB-IRIS: a report of 4 children.. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 2012. DOI: 10.1016/j.ejpn.2012.04.005.

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