Rheumatoid arthritis (RA) is a subacute or chronic inflammatory disease (polyarthropathy) of unknown cause in which the body's immune system attacks joints and other tissues. Onset is usually between 25 and 50years, women are more likely to develop RA than men (3x more). Heavy long - term smoking is a very strong risk factor for RA as well as other lungs affections (cancer most of all).
Primary sites of inflammation are synovial membranes and articular structures. X-rays generally have not been helpful to detect the presence of early rheumatoid arthritis because they cannot show soft tissue. Swelling and pain in the joints occur for at least 6 weeks before a diagnosis of RA is considered. The pattern of joints affected is usually symmetrical. Although RA almost always develops in the wrists and knuckles, the knees and small foot joints are often affected as well. Indeed, many joints may be involved (cervical spine, shoulders, elbows, tips, temporomandibular joint, inner ear). RA does not usually show up in the fingertips, where osteoarthritis is common. Disease is characterized with relapses and remissions.
Extraarticular RA is more common in male’s age 50-60years. Patients are asymptomatic; most have arthritis, positive rheumatoid factor and cutaneous nodules. Lung changes are found in 90% patients. Pulmonary involvement is a serious complication of rheumatoid arthritis and may be seen as airway disease, rheumatoid nodules, interstitial lung disease and pleurisy.
In literature are described a broad range of pathologic features in the lungs. Four predominant CT patterns are: usual interstitial pneumonia (UIP), nonspecific interstitial pneumonia (NSIP), bronchiolitis obliterans (BO) and organizing pneumonia (OP). Ground-glass opacity or reticulation is the most common CT finding. Honeycombing, traction bronchiectasis and architectural distortion also frequently occurred. The multiplicity of CT patterns is commonly seen and might help differentiate these patients from those with idiopathic diffuse lung disease. Necrobiotic pulmonary nodules are well established among the extra-articular manifestations of RA, but their manifestation is rare. The nodules may be solitary or, more commonly, multiple, ranging in size from a few millimeters to 7cm or more. They are well-circumscribed, localized peripheral, predominantly in lower lobes. The nodules may multiply or regress independently of the disease process elsewhere, and during their existence they may calcify or cavitate and even lead to pyopneumothorax. Necrobiotic nodules occur more frequently in men than woman, compared to the female predominance of rheumatoid arthritis.
Differential diagnosis of lung nodules is not easy. Nodules can imitate bronchial carcinoma radiologically and bronchoscopically. In differential diagnosis of tumor can help irregularity inner lining and cavitations only in 10% of lung tumours. Wegener’s granulomatosis shows nodules with frequent cavitation, but pleural effusion and hilar lymph node enlargement is very rare. Also in full-blown form kidneys, nose and paranasal sinuses are involved. Sarcoidosis is commonly associated with some type of reticulonodular lung disease, but can simulate metastatic lung disease.
Treatment is based on steroids and immunosuppressive therapy.
5 years survival is 40%, death is usually caused by infection, respiratory failure, cor pulmonale or amyloidosis.