M. Grouhi et al., Long-term remission for disseminated Mycobacterium avium-intracellulare complex associated with antibody deficiency, PEDIATRICS, 103(1), 1999, pp. E131-E133
Mycobacterium avium-intracellulare (MAI) is a ubiquitous organism with limi
ted virulence in the immunocompetent host. Disseminated disease is associat
ed with a high mortality rate. Except for localized cervical adenitis, MAI
disease is rare in immunocompetent children. We report a child with antibod
y deficiency (dysgammaglobulinemia) and disseminated MAI infection, in whom
complete, long-term remission was attained with multiple antimycobacterial
therapy.
The patient presented with progressive cervical lymphadenopathy and hepatom
egaly at 7 years of age. A lymph node biopsy showed acid-fast bacilli and g
ranulomas. Despite a transient response to conventional antituberculous the
rapy, including isoniazid and rifampin, his symptoms progressed. Cultures f
rom blood, bone marrow, spleen, and cervical lymph node tissues revealed an
MAI organism. Subsequent treatment using a combination of clarithromycin,
amikacin, and ethambutol for 16 months resolved clinical symptoms, and subs
equent blood culture results became negative. By the time of this report, t
he patient has been disease-free for 4 years.
Multiple-drug therapy is promising for the treatment of MAI in children wit
h antibody deficiency; however, the selection of antiinfective drugs should
include a member of the newer macrolide family.