We present a case of a patient with cystic fibrosis who was thought to be c
olonized with Mycobacterium abscessus for 13 yr prior to developing clinica
lly apparent mycobacterial infection. However, histologic evidence indicate
d that invasive mycobacterial disease was present from the onset. While acc
epting that chronic endobronchial colonization with atypical mycobacteria m
ay occur in patients with cystic fibrosis, the repeated isolation of mycoba
cteria from the sputum of these patients should alert the clinician to the
possibility of indolent disease. Early consideration of treatment for this
infection should occur in any patient with cystic fibrosis in whom there is
an unexplained deterioration in lung function. The recent introduction of
high dose ibuprofen raises concerns about its possible contribution to the
progression of the infection.