Abstract
Sarcoidosis is a common, multisystem granulomatous disease of unknown cause. The disease occurs worldwide, frequently affects young adults, and presents with bilateral hilar adenopathy, pulmonary infiltrates, uveitis, skin lesions, hypercalcemia, and hepatic granulomas. Diagnosis of sarcoidosis is based on the presence of typical multisystem clinical and radiographic features with histologic evidence of non-caseating granulomas in the affected tissue. Natural course of sarcoidosis varies with type of the disease: Acute sarcoidosis with erythema nodosum, uveitis, and bilateral hilar adenopathy clears with in a period of 12–18 months, particularly in the Caucasian patients; chronic disease with pulmonary infiltrate/fibrosis, lupus pernio, bone-cysts, nephrocalcinosis, chronic uveitis, and upper airway disease pursues an indolent course and respond minimally to treatment. Since the cause of sarcoidosis is not known; there is no specific cure for it. Corticosteroids are effective mode of therapy to suppress granulomatous inflammation, but they do not change the disease course.
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Mahmoudi, M., Sharma, O.P. (2012). Sarcoidosis. In: Mahmoudi, M. (eds) Challenging Cases in Pulmonology. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-7098-5_15
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DOI: https://doi.org/10.1007/978-1-4419-7098-5_15
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