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- W3148447411 abstract "Löfgren’s syndrome presents as acute sarcoid arthritis, with a triad of hilar adenopathy, acute polyarthritis and erythema nodosum. Löfgren’s syndrome is self-limited, erythema nodosum, hilar adenopathy and acute polyarthritis usually resolve within a few weeks to months, however polyarthritis can last for up to 2 years. Treatment involves symptomatic control with NSAIDs/colchicine or oral glucocorticoids until symptoms resolve, if disease is resistant to these therapies, hydroxychloroquine, methotrexate or infliximab can be used. Löfgren’s syndrome is a rare presentation of sarcoidosis occurring in only about 5–10% of sarcoid patients. It is, however, important to recognize as it is the most common form of acute sarcoid arthritis and prompt treatment can prevent unnecessary prolonged discomfort for patients." @default.
- W3148447411 created "2021-04-13" @default.
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- W3148447411 date "2021-03-30" @default.
- W3148447411 modified "2023-09-26" @default.
- W3148447411 title "Löfgren’s Syndrome" @default.
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- W3148447411 doi "https://doi.org/10.5772/intechopen.97154" @default.
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