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Volume 90, Issue 4, Pages 213-224 (July 2010)


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The chemotherapy of tuberculous lymphadenopathy in children

P.R. DonaldCorresponding Author Informationemail address

Received 29 March 2010; received in revised form 26 April 2010; accepted 4 May 2010. published online 03 June 2010.

Summary 

The chemotherapy of tuberculous lymphadenopthy, the commonest form of extra-pulmonary tuberculosis, is reviewed and a recommendation made for the treatment of this condition in children. Fifteen papers were identified recording the treatment and follow-up of 1133 adults and children with six-month isoniazid and rifampicin based regimens. In 32 (2.8%) cases treatment was recommenced, but in only one case was relapse microbiologically confirmed and in a further four histology was compatible with tuberculosis. Four studies enrolling 484 adults and children, record the follow-up of patients receiving 6–18 months treatment with INH and RMP based regimens; treatment was recommenced in 24 (5%), but in no case was relapse confirmed microbiologically. Five papers describe the treatment and follow-up of 246 adults and children receiving nine-month INH and RMP based regimens and record the recommencement of treatment in 4 (1.6%) cases, but in no case was relapse confirmed microbiologically. Four controlled studies failed to show any advantage for treatment regimens longer than six months. Paradoxical recurrence and worsening of clinical features was common during and following all regimens being recorded in from 3 to20% of patients. Very seldom were these events accompanied by evidence of culture of Mycobacterium tuberculosis to confirm microbiological failure to respond or relapse. Tuberculous lymphadenopathy in children can be safely treated with six months of INH and RMP with PZA given for the first two months and accompanied by EMB in areas with a high prevalence of drug resistance. Every effort should be made to confirm the diagnosis and possible relapses microbiologically.

Department of Paediatrics and Child Health and The Division of Molecular Biology and Human Genetics, the MRC Centre for Molecular and Cellular Biology and the DST/NRF Centre of Excellence for Biomedical TB Research, Faculty of Health Sciences, Stellenbosch University, South Africa

Corresponding Author InformationDepartment of Paediatrics and Child Health, University of Stellenbosch, PO Box 19063, 7505 Tygerberg, South Africa. Tel.: +27 219839592; fax: +27 219389138.

PII: S1472-9792(10)00062-4

doi:10.1016/j.tube.2010.05.001


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