|
|
||||||||
Original Report |
1 Department of Radiology and Center for Imaging Science, Samsung Medical
Center, Sungkyunkwan University School of Medicine, 50 Ilwon-Dong, Kangnam-Ku,
Seoul 135-710, Korea.
2 Division of Pulmonary and Critical Care Medicine, Department of Medicine,
Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul
135-710, Korea.
Received October 25, 2002;
accepted after revision February 14, 2003.
Address correspondence to K. S. Lee.
Abstract
|
|
|---|
CONCLUSION. The main radiologic and CT manifestations of M. abscessus lung infection are bilateral small nodular opacities, bronchiectasis, and cavity formation.
|
|
|---|
To our knowledge, the CT findings of M. abscessus lung infection have not been previously described. The purpose of our study was to review the radiographic and CT findings in patients with M. abscessus lung infection.
|
|
|---|
All 12 patients had three or more sputum specimens with positive smears for acid-fast bacilli and positive cultures for M. abscessus. Transbronchial lung biopsy via fiberoptic bronchoscopy performed in six patients revealed either granulomatous inflammation and caseous necrosis or positive culture results for M. abscessus. None of the 12 patients was immunocompromised. Although 11 of 12 patients had supposedly been treated for tuberculosis, detailed histories about how the diagnosis of pulmonary tuberculosis had been reached were not available. The patients had no other preexisting lung diseases.
All 12 patients had radiographs, and 10 patients had chest CT scans available. The interval between isolation of the M. abscessus bacteria and the initial radiographic and CT examinations ranged from 0 to 120 days (mean, 13.1 days) and from 0 to 230 days (mean, 52.4 days), respectively. All patients had follow-up radiographs, with the intervals between the initial and the final follow-up examinations ranging from 4 to 34 months (mean, 14.2 months). In four patients, specific treatment (amikacin, cefoxitin, and clarithromycin) for M. abscessus was given during the follow-up periods.
Imaging Technique
Posteroanterior chest radiographs were obtained with a computed radiography
system (FCR 9501, Fuji, Tokyo, Japan). Unenhanced CT scans were obtained with
either a HiSpeed Advantage (three patients) or a LightSpeed Advantage Q/xi
scanner (seven patients) (both, General Electric Medical Systems, Milwaukee,
WI). All CT data were reconstructed using a bone algorithm. On the HiSpeed
Advantage scanner, we used a thin-section CT technique (1-mm collimation, 120
kVp, 170 mA, 10-mm intervals). On the LightSpeed Advantage Q/xi multidetector
CT scanner, we obtained volumetric scan data (2.5-mm collimation, 120 kVp, 70
mA, pitch of 6, reconstructed with 2.5-mm thickness) through the thorax.
Review of Radiographs and CT Scans
Initial and follow-up radiographs and CT scans were reviewed jointly by
three chest radiologists who were aware that all patients had proven
nontuberculous mycobacterial pulmonary infections; the final decision on the
findings was reached by consensus. On the radiographs, the observers assessed
the presence of reticulonodular opacities, nodules, cavitation, consolidation,
and volume decrease. For the purpose of analysis, we divided each lung into
three zones, and each zone was assessed separately. Lesions were considered to
be in the upper zone of the lung if cephalad to the aortic arch, in the lower
zone if caudad to the inferior pulmonary vein, and in the middle zone if seen
between the two other zones. The overall extent of each pattern was estimated
by calculating the involved zones of the 72 lung zones in 12 patients (six
zones in each patient). The chest radiographic findings were classified as
showing either upper lobe cavitary disease (i.e., classic pulmonary
nontuberculous mycobacterial infection)
[5] or nodular bronchiectatic
disease [1]. A combination of
cavities, consolidation, volume decrease, and pleural thickening in the upper
lobes was considered upper lobe cavitary disease, regardless of whether
reticulonodular opacities were present
[4]. Bilateral nodular or
reticulonodular changes that were predominantly seen in the middle and lower
lung zones without visible cavities or marked volume decrease of the lobes or
the lungs were considered nodular bronchiectatic disease.
The CT scans available for 10 patients were evaluated with regard to the presence or absence of well-defined nodules, branching centrilobular nodules (i.e., the tree-in-bud pattern), consolidation, cavity formation, volume loss, and bronchiectasis. When present, the morphology of bronchiectasis was recorded as being cylindrical, varicose, or cystic [6]. The extent of of overall involvement and of the involvement of each pattern was estimated by calculating the involved lobes of the 60 lung lobes in 10 patients (six lobes in each patient; each lingular segment was considered a lobe). The presence or absence of mediastinal adenopathy and pleural effusion or thickening was also recorded.
On follow-up radiographs, we evaluated the changes in overall extent and each pattern of abnormalities over time in each patient.
|
|
|---|
|
|
|
|
|
Overall, the nodular bronchiectatic form of nontuberculous mycobacterial lung infection (Fig. 1A, 1B, 1C) was observed in seven patients, and the upper lobe cavitary form of infection (Fig. 2A, 2B) was seen in five. The seven patients with nodular bronchiectatic disease had reticulonodular opacities as an isolated finding on radiographs. The five patients with upper lobe cavitary disease included four patients with a combination of a lung cavity, volume loss, and consolidation and one patient with a lung cavity, volume loss, and reticulonodular opacities.
Radiographic abnormalities were patchy in distribution in all patients except one in whom diffuse reticulonodular opacities were present throughout both lungs. Lymph node enlargement was not seen on the radiographs of any patients.
On CT, the most common findings were branching nodular opacities (i.e., the tree-inbud pattern) and bronchiectasis, each finding being seen in nine (90%) of the 10 patients for whom CT scans were available (Fig. 1A, 1B, 1C). Branching nodular opacities (53% or 32/60 lobes) were unilateral in three patients and bilateral in six and showed no lobar predominance. Bronchiectasis (43% or 26/60 lobes) was unilateral in five patients and bilateral in four and showed no lobar predominance. Bronchiectasis was mainly cylindrical in 16 lobes, cystic in eight, and varicose in two. Well-defined nodules smaller than 1 cm in diameter (35% or 21/60 lobes) (Fig. 1A, 1B, 1C) were identified in seven patients; the nodules were distributed bilaterally in six patients and unilaterally in one without lobar predilection. Cavities (17% or 10/60 lobes) were seen in four patients (Fig. 2A, 2B). The cavities were unilateral in three patients and bilateral in one and mainly involved the upper lobes. Other CT findings included air-space consolidation (13% or 8/60 lobes) seen in four patients, lobar volume loss (13% or 8/60 lobes) in three patients, pleural thickening in three patients, and mediastinal lymphadenopathy in two patients.
On follow-up radiographs, the overall extent of parenchymal lesions decreased in four patients (Fig. 3A, 3B), remained unchanged in seven, and increased in one. The extent of reticulonodular opacities remained unchanged in seven of the 11 patients in whom opacities were seen, decreased in three, and increased in one. Both the number and size of cavities in the five patients in whom cavities were seen decreased in three patients and showed no change in two. Volume decrease remained unchanged in four of the five patients in whom this condition was seen and improved in one. The extent of consolidation decreased in two of the four patients in whom consolidation occurred and remained unchanged in two. In four patients who received specific antibiotic therapy, interval changes were diverse: in one patient, an interval increase in the extent of reticulonodular opacity was observed; in two, the disease was stationary; and in one, an interval decrease in the extent of both the consolidation and the cavity was noted.
|
|
|
|
|---|
Griffith et al. [3] found the most frequent radiologic pattern to be reticulonodular lesions. The disease frequently was bilateral (77%) and involved the upper lobes (88%). Multilobar involvement was also common. Cavitation was seen in 16% of patients. In our study, we also found reticulonodular opacities (92% or 11/12 patients) to be the most common pattern of abnormality on radiographs. However, we saw cavitary lesions more frequently (42% or 5/12 patients) than Griffith and colleagues saw in their study (16% of patients).
To our knowledge, the CT findings of M. abscessus lung infection have not been previously described. The predominant abnormalities seen in our study were branching nodular opacities (tree-in-bud pattern) and bronchiectasis, each being seen in nine (90%) of 10 patients with CT scans. These findings were most commonly bilateral and showed no lobar predominance. Other common findings included well-defined nodules smaller than 1 cm in diameter, which we found in seven of the patients; consolidation, which we found in five; and cavities, which we found in four.
CT findings of the lung abnormalities caused by M. avium-intracellulara complex infection have been reported to be limited to the right middle lobe or the lingular division [5], but we found that abnormalities of bronchiectasis, bronchiolitis, and nodules in patients with M. abscessus lung infection commonly showed no predilection for these anatomic locations. Upper and lower lobes were as frequently involved as were middle lobes or the lingular division. Therefore, our CT findings for M. abscessus were similar to those described for Mycobacterium chelonae lung infection [2], another rapidly growing mycobacterium. In the study by Hazelton et al. [2] of 14 patients with M. chelonae lung infection, common CT findings such as bronchiectasis, nodules, and consolidation were widely distributed in both lungs.
In our study, cavitary lesions were seen in five (42%) of 12 patients on radiography and four (40%) of 10 patients on CT. Because most patients (11/12) had a history of Mycobacterium tuberculosis infection, we are not certain whether cavities were caused by previous tuberculous infection or M. abscessus infection itself. However, because tuberculous infection is a predisposing condition for nontuberculous mycobacterial infection, a distinction as to the cause of the cavitary lesions may not be important.
In our study, the radiographic findings of reticulonodular lesions with bilateral and multilobar distribution coincided with the CT findings of widespread branching nodular opacities or tree-in-bud appearance, bronchiectasis, and small nodules. Cavitary and consolidative lesions seen on radiographs in volume-decreased upper lobes corresponded to the cavities, consolidations, and parenchymal bands in retracted lobes seen on CT scans. In addition, our radiologic findings showed interval improvement in some patients but no change or interval progression in others. Some patients showed mixed interval changes; patterns in some patients showed improvement, whereas patterns in others showed progression. Although we believe that these diverse interval changes represent the chronic and persistent nature of the infection, we cannot explain the mechanism of spontaneous interval decrease in the extent of disease over time in some patients.
We did not encounter a patient with pulmonary infection involving multiple organisms, but the possibility that a patient could have such an infection should be kept in mind [3, 8]. In the study by Griffith et al. [3], 8% of the patients with rapidly growing mycobacterial lung disease had coexisting M. avium-intracellulara complex infection. Some patients with M. avium-intracellulara complex lung disease also had M. abscessus isolated in their sputum cultures some time during the course of their disease [8]. Therefore, deciding which of the two mycobacteria is the most important pathogen to treat may be difficult.
The treatment of M. abscessus is complex [7, 9]. M. abscessus is generally susceptible only in vitro to parenteral antibiotics such as amikacin, cefoxitin, and imipenem and to the newer oral macrolides such as clarithromycin [10], making surgical resection of localized disease the only effective long-term therapy for patients infected with the organism [3, 7]. Although both M. chelonae and M. abscessus belong to M. chelonae group, M. chelonae tends to be more resistant than M. abscessus to antimicrobial drugs [10].
We observed no imaging features that allowed distinction of M. abscessus lung infection from M. chelonae infection [2] in our study. In addition, imaging findings of M. abscessus were similar to those of M. avium-intracellulara complex lung infection except that in patients with M. avium lung infection, most nodular bronchiectasis was either isolated to or most severe in the middle lobes or the lingula [5]. As in previous descriptions of rapidly growing M. chelonae and M. abscessus lung infections [2, 3], we found that the distribution of nodular bronchiectasis was rather more extensive and showed no zonal predominance.
In conclusion, bilateral multilobar bronchiectasis and bronchiolitis or upper lobe cavities combined with consolidations in volume-decreased upper lobes are the predominant radiographic and CT findings in patients with M. abscessus lung infection. These patterns of parenchymal abnormalities on both chest radiographs and CT scans are similar to the patterns of lung infection seen with other rapidly growing mycobacteriaM. chelonae or M. avium-intracellulara complex. However, the lung involvement seen in patients with M. abscessus lung infection is more extensive than that seen in patients with M. avium-intracellulara complex infection.
Acknowledgments
We thank Nestor L. Müller for helping us to revise this
manuscript.
|
|
|---|
This article has been cited by other articles:
![]() |
L. B. Gadkowski and J. E. Stout Cavitary Pulmonary Disease Clin. Microbiol. Rev., April 1, 2008; 21(2): 305 - 333. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Martinez, H. P. McAdams, and C. S. Batchu The Many Faces of Pulmonary Nontuberculous Mycobacterial Infection Am. J. Roentgenol., July 1, 2007; 189(1): 177 - 186. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. J. Ryu, E. J. Kim, W.-J. Koh, H. Kim, O J. Kwon, and J. H. Chang Toll-Like Receptor 2 Polymorphisms and Nontuberculous Mycobacterial Lung Diseases. Clin. Vaccine Immunol., July 1, 2006; 13(7): 818 - 819. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. K. Field and R. L. Cowie Lung Disease Due to the More Common Nontuberculous Mycobacteria Chest, June 1, 2006; 129(6): 1653 - 1672. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-J. Koh, O. J. Kwon, K. Jeon, T. S. Kim, K. S. Lee, Y. K. Park, and G. H. Bai Clinical significance of nontuberculous mycobacteria isolated from respiratory specimens in Korea. Chest, February 1, 2006; 129(2): 341 - 348. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-J. Koh, O. J. Kwon, E. J. Kim, K. S. Lee, C.-S. Ki, and J. W. Kim NRAMP1 Gene Polymorphism and Susceptibility to Nontuberculous Mycobacterial Lung Diseases Chest, July 1, 2005; 128(1): 94 - 101. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-J. Koh, K. S. Lee, O J. Kwon, Y. J. Jeong, S.-H. Kwak, and T. S. Kim Bilateral Bronchiectasis and Bronchiolitis at Thin-Section CT: Diagnostic Implications in Nontuberculous Mycobacterial Pulmonary Infection Radiology, April 1, 2005; 235(1): 282 - 288. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. J. Jeong, K. S. Lee, W.-J. Koh, J. Han, T. S. Kim, and O J. Kwon Nontuberculous Mycobacterial Pulmonary Infection in Immunocompetent Patients: Comparison of Thin-Section CT and Histopathologic Findings Radiology, June 1, 2004; 231(3): 880 - 886. [Abstract] [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |