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Sarcoidosis

Sarcoidosis is an immune system disorder characterised by non-necrotising granulomas (small inflammatory nodules). Virtually any organ can be affected, however, granulomas most often appear in the lungs (D860) or the lymph nodes (D861). more...

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Symptoms can occasionally appear suddenly but more often than not appear gradually. When viewing X-rays of the lungs, sarcoidosis can have the appearance of tuberculosis or lymphoma.

Epidemiology

Sarcoidosis occurs throughout the world in any race. It is more commonly seen in blacks than whites, primarily people of northern European descent in the latter case. Pulmonary involvement is the most common presentation of sarcoidosis.

Signs and symptoms

Sarcoidosis is a systemic disease that can affect any organ. Common symptoms are vague, such as fatigue unchanged by sleep, lack of energy, aches and pains, dry eyes, blurry vision, shortness of breath, a dry hacking cough or skin lesions. The cutaneous symptoms are protean, and range from rashes and noduli (small bumps) to erythema nodosum or lupus pernio.

The combination of erythema nodosum, bilateral hilar lymphadenopathy and arthralgia is called Lofgren syndrome. This syndrome has a relatively good prognosis.

Renal, liver, heart or brain involvement may cause further symptoms and altered functioning. Manifestations in the eye include uveitis and retinal inflammation, which may result in loss of visual acuity or blindness. Sarcoidosis affecting the brain or nerves is known as neurosarcoidosis.

The combination of anterior uveitis, parotitis and fever is called Heerfordt-Waldenstrom syndrome. (D868)

Hypercalcemia (high calcium levels) and its symptoms may be the result of excessive vitamin D production.

Sarcoidosis most often manifests as a restrictive disease of the lungs, causing a decrease in lung volume and decreased compliance (the ability to stretch). The vital capacity (full breath in, to full breath out) is decreased, and most of this air can be blown out in the first second. This means the FEV1/FVC ratio is increased from the normal of about 80%, to 90%.

Causes and pathophysiology

No direct cause of sarcoidosis has been identified, although there have been reports of cell wall deficient bacteria that may be possible pathogens. These bacteria are not identified in standard laboratory analysis. It has been thought that there may be a hereditary factor because some families have multiple members with sarcoidosis. To date, no reliable genetic markers have been identified, and an alternate hypotheses is that family members share similar exposures to environmental pathogens. There have also been reports of transmission of sarcoidosis via organ transplants.

Sarcoidosis frequently causes a dysregulation of vitamin D production; extrarenal (outside the kidney) production can be marked. Production of vitamin D goes on outside the kidneys. This results in elevated levels of the hormone 1,25-dihydroxyvitamin D and symptoms of hypervitaminosis D that may include fatigue, lack of strength or energy, irritability, metallic taste, temporary memory loss or cognitive problems. Physiological compensatory responses (e.g. suppression of the parathyroid hormone levels) may mean the patient does not develop frank hypercalcemia.

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Corticosteroids for pulmonary sarcoidosis
From American Family Physician, 11/1/05 by Mark H. Ebell

Clinical Question

Do inhaled or oral corticosteroids improve outcomes for patients with pulmonary sarcoidosis?

Evidence-Based Answer

Patients who take oral corticosteroids are more likely to show improvement in their chest radiographs than those taking placebo, although improvements in symptoms and lung function are less certain. The typical dosage used in randomized trials was 20 mg daily or 40 mg every two days tapered over several months.

Practice Pointers

Sarcoidosis is a multisystem disease that often affects the lungs. Pulmonary sarcoidosis is characterized by cough, breathlessness, and progressive respiratory failure. Corticosteroids are the most widely used treatment, but until now, the evidence had not been reviewed systematically. Other treatments, such as methotrexate, antimalarial drugs, cyclosporine (Sandimmune), and the immunomodulator infliximab (Remicade), have been less well studied. (1)

Paramothayan and associates found 12 randomized controlled trials using different doses and routes of administering corticosteroids. only two were double-blinded, and only two used adequate concealment of allocation. The 1,051 participants involved in the studies were at various stages of histology-confirmed disease. The studies used a variety of outcomes, primarily symptoms, lung function, and chest radiograph findings. Few data were available for more than two years of follow-up, and none of the studies measured the impact on mortality. In general, studies were small, most with fewer than 50 participants.

Four studies compared oral steroids with placebo, and two compared oral steroids with no treatment. of the two largest studies, one used a tapering dose of 20 to 10 mg daily and the other a tapering dose of 40 to 20 mg every two days. The researchers found a consistent benefit in terms of improved chest radiograph appearance at the end of follow-up (70 versus 49 percent, P = .04, number needed to treat = 5). However, they found no consistent evidence of symptomatic improvement or improvement in measures of lung function. Comparisons of inhaled steroids with placebo did not show any consistent benefit.

Paramothayan NS, et al. Corticosteroids for pulmonary sarcoidosis. Cochrane Database Syst Rev 2005;(2):CD001114.

REFERENCES

(1.) Baughman RP, Lower EE, du Bois RM. Sarcoidosis. Lancet 2003;361: 1111-8.

MARK H. EBELL. M.D., M.S.

COPYRIGHT 2005 American Academy of Family Physicians
COPYRIGHT 2005 Gale Group

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