Autoimmune > Ankspondylitis

Ankylosing Spondylitis:

View cases of ankylosing spondylitis

Clinical:

Ankylosing spondylitis occurs in about 0.15% of white males, is uncommon in blacks, and the male to female ratio is about 10:1 [3]. The peakk incidence is between the ages of 15-35 years [5]. Up to 95% of patients with ankylosing spondylitis are HLA-B27 (and 2-20% of persons that are HLA-B27 positive will develop ankylosing spondylitis) [3]. Symptoms of the disorder and typically isolated to the inflammatory spinal disease, but ocular (uveitis or iritis), cardiovascular (aortic insufficiency or dilatation), and pulmonary involvement may also occur [3].


The reported incidence of pulmonary disease varies, but it probably develops in only about 1% of patients and it is characterized by upper lobe fibrotic lung disease which tends to mimic old TB. The lung disease is usually not evident until ten or more years after the onset of bone disease (in patients with advanced stage disease). In fact, lung disease is generally identified only in patients with severe bone changes, but patients are usually asymptomatic [3]. Lung disease begins unilaterally and then becomes bilateral. The cause of the fibrobullous changes is not known [3] and it is not felt to be a result of chest wall immobility. Secondary superinfection of the cavities with Aspergillus (i.e.: mycetoma formation) may also be seen in these patients.

 

Ankylosing spondylitis is also associated with aortitis- aortic root disease and aortic valve disease can be found in up to 80% of patients [4]. Aortic wall thickening can be found at imaging in about 60% of affected patients [4].

X-ray:

Pulmonary parenchymal findings may mimic those of TB infection with apical fibrocavitary changes and cyst formation. If fungal superinfection has occurred a mycetoma may be identified.  High-resolution CT can detect additional abnormalities not identified by plain film radiographs (2).

REFERENCES:

(1) Semin Arthritis Rheum 1989; Boushea DK, et al. The pleuropulmonary manifestations of ankylosing spondylitis. 18 (4): 277-281 (No abstract available)

(2) AJR 1997; Fenlon HM, et al. Plain radiographs and thoracic high-resolution CT in patients with ankylosing spondylitis. 168: 1067-1072

(3) J Thorac Imaging 1992; Tanoue LT. Pulmonary involvement in collagen vascular disease: A review of the pulmonary manifestations of the Marfan syndrome, ankylosing spondylitis, Sjogren's syndrome, and relapsing polychondritis. 7 (2): 62-77

(4) Radiographics 2011; Restrepo CS, et al. Aortitis: iimng spectrum of the infectious and inflammatory conditions of the aorta. 31: 433-451

(5) Radiographics 2012; Capobianco J, et al. Thoracic manifestations of collagen vascular diseases. 32: 33-50

 

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