Pulmonary Mycobacterium avium complex (MAC) infection is a type of non-tuberculous mycobacterial (NTM) infection. It is relatively common and continues to pose significant therapeutic challenges. In addition, in many instances the role of MAC in pulmonary pathology remains controversial.
Mycobacterium avium complex (MAC) infections often occur patients with pre-existing pulmonary disease or those with depressed immunity. It is however also seen frequently in otherwise healthy patients, with a predilection for older women who deliberately suppress cough reflex (Lady Windermere syndrome) 1-3.
A number of patient groups have been associated with increased risk of pulmonary MAC. They include 2-3:
- elderly, white, thin women : nodular bronchiectatic form (see below)
- middle-aged or elderly males who are smokers or alcoholics : upper lobe cavitary form (see below)
- immunocompromised patients e.g. AIDS
- patients with cystic fibrosis : MAC isolated in up to 13% of patients
- patients with alpha-1-antitrypsin deficiency
- other causes of bronchiectasis
- chronic obstructive pulmonary disease (COPD)
Isolation of MAC from a patient's lung is not pathognomonic of infection, as colonisation is common, and thus microbiology needs to be correlated with clinical and radiographic appearances 2-3.
Pulmonary MAC infection is typically insidious, with a chronic cough usually productive of purulent sputum being most common. Haemoptysis and constitutional symptoms are not typical 2.
Mycobacterium avium and Mycobacterium intracellulare are now considered together, and referred to as Mycobacterium avium complex (MAC) or Mycobaverium avium-intracellulare. They cannot be distinguished on the grounds of human pathologic manifestation or imaging features, and are treated similarly, although M avium has a predilection for chickens where as M intracellulare prefers rabbits 2-3.
They are ubiquitous organisms, found in both fresh and salt water, but do not tend to cause human disease.
Patients with MAC infection are, unlike those with pulmonary tuberculosis, not contagious 2.
Two main forms of pulmonary MAC infections are recognised 3:
- nodular bronchiectatic form
- upper lobe cavitary form
Bronchiectasis with associated centrilobular nodules is the dominant feature in the former, which unlike pulmonary tuberculosis does not have a predilection for the upper lobes. In elderly white females the right middle lobe and lingula are particularly affected.
In upper lobe cavitary form, thin walled cavities with overall volume loss and fibrosis are the dominant feature, often also with features of endobronchial spread with tree-in-bud opacities seen elsewhere.
Upper zone cavities may also be seen with associated volume loss and scarring 3.
The most common findings of MAC infections include 1-2:
- bronchiectasis and bronchial wall thickening : most common findings
- ground-glass opacities
- small centrilobular nodules and tree-in-bud appearance
- patchy consolidation
- predilection for the right middle lobe and lingula is seen particularly in elderly white women 2
- pleural thickening may be seen, usually adjacent to parenchymal change
- upper lobe cavitation may also be seen, although it is more characteristic of pulmonary tuberculosis
Treatment and prognosis
Many treatment regimes have been published, with no clear gold-standard evident, although as is the case with pulmonary TB, multi-drug therapy is ideal to avoid resistance 2.
In patients who are unable to tolerate medical management, and who have adequate respiratory reserve, resection of affect portions of the lung may be undertaken. Complications of surgery include bronchopleural fistulas, haemoptysis and empyema 2.
In patients in whom isolates of MAC are not clearly pathogenic, follow-up is required, keeping in mind that evidence of radiographic progression may take a number of year to be convincing 3.
Prognosis depends on the form of disease. In the upper lobe cavitary form, lung destruction is usually progressive and can lead to respiratory failure and death if successful treatment is not instituted.
In patients with nodular bronchiectatic form (Lady Windermere syndrome) the disease is much more indolent, however eventually this form may also lead to enough parenchymal damage to result in respiratory failure and death 3.
Mycobacterium tuberculosis pulmonary infection
- bronchiectasis less commonly the dominant feature 1
- changes usually upper lobes 1
- For associated bronchiectasis : see other causes of bronchiectasis
The underlying pulmonary abnormality (e.g. COPD, pneumoconiosis etc..) may dominate the radiographic appearance.
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- 1. Primack SL, Logan PM, Hartman TE et-al. Pulmonary tuberculosis and Mycobacterium avium-intracellulare: a comparison of CT findings. Radiology. 1995;194 (2): 413-7. Radiology (abstract) - Pubmed citation
- 2. Field SK, Fisher D, Cowie RL. Mycobacterium avium complex pulmonary disease in patients without HIV infection. Chest. 2004;126 (2): 566-81. doi:10.1378/chest.126.2.566 - Pubmed citation
- 3. Müller NL, Franquet T, Lee KS et-al. Imaging of pulmonary infections. Lippincott Williams & Wilkins. (2007) ISBN:078177232X. Read it at Google Books - Find it at Amazon
Synonyms & Alternative Spellings
|Synonyms or Alternative Spelling||Include in Listings?|
|Pulmonary Mycobacterium avium complex infections||✗|
|Pulmonary Mycobacterium avium-intracellulare complex infections||✗|
|Pulmonary Mycobacterium avium complex (MAC)||✗|
|Pulmonary Mycobacterium avium-intracellulare (MAI) infections||✗|
|Pulmonary Mycobacterium avium-intracellulare complex (MAIC) infections||✗|
|Pulmonary manifestations of non-tuberculous mycobacterial infections||✓|