C. Pierreaudigier et al., FATAL DISSEMINATED MYCOBACTERIUM-SMEGMATIS INFECTION IN A CHILD WITH INHERITED INTERFERON-GAMMA RECEPTOR DEFICIENCY, Clinical infectious diseases, 24(5), 1997, pp. 982-984
Mycobacterium smegmatis is a common environmental mycobacterium that w
as first identified in 1884, yet is a rare pathogen in humans. The few
AL smegmatis infections reported to date have been localized and have
occurred in association with a primary lesion in otherwise immunocomp
etent individuals. To our knowledge, no case of disseminated ai. smegm
atis infection has ever been reported, even in patients with severe im
mune deficiencies. We report a case of disseminated mycobacterial infe
ction that was diagnosed in a 3-year-old girl, The pathogen was not id
entified as M. smegmatis until the patient was 6 years old. Her condit
ion gradually worsened, and she died when she was 8 years old despite
appropriate antimycobacterial therapy. No other opportunistic infectio
ns were documented, Immunological investigations revealed an inherited
interferon gamma receptor I deficiency. This report identifies d. sme
gmatis as a new opportunistic agent that may be responsible for dissem
inated disease in immunocompromised individuals.