Published 28 August 2009, doi:10.1136/bmj.b3206
Cite this as: BMJ 2009;339:b3206

Clinical Review

Sarcoidosis

Owen J Dempsey, consultant chest physician1, Edward W Paterson, specialist registrar in respiratory medicine1, Keith M Kerr, professor of pulmonary pathology2, Alan R Denison, clinical senior lecturer3

1 Department of Respiratory Medicine, Aberdeen Royal Infirmary, Foresterhill, Aberdeen AB25 2ZN, 2 Aberdeen University Medical School, Foresterhill, Aberdeen AB25 2ZD , 3 Aberdeen Biomedical Imaging Centre, University of Aberdeen Royal Infirmary, Foresterhill, Aberdeen AB25 2ZD

Correspondence to: O J Dempsey owen.dempsey@nhs.net

The first 150 words of the full text of this article appear below.


Sarcoidosis is a multisystem granulomatous disease of unknown cause, typically affecting young and middle aged adults
Three thousand new cases are diagnosed each year in the United Kingdom
Any organ can be affected—mostly lungs, skin, and eyes—and patients often feel tired and generally unwell
Most patients do not need systemic treatment, and disease often regresses spontaneously, especially in those presenting with erythema nodosum
A minority have potentially life threatening progressive organ dysfunction; these patients need active management including oral corticosteroids


Around 3000 new cases of sarcoidosis are diagnosed each year in the United Kingdom.1 General practitioners play a key role in the early recognition of the most common clinical presentations of this multifaceted disease, and they usually direct initial assessment and specialist referral. Although prognosis is excellent for most patients, a minority will develop life threatening complications and may need potentially toxic treatments. Most patients are young and understandably alarmed . . . [Full text of this article]


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