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- W2051289796 abstract "Erdheim-Chester disease (ECD) is a rare form of non-Langerhans histiocytosis with heterogeneous clinical manifestations. The most common presentation is bone pains typically involving the long bones. Approximately 75% of the patients develop extraskeletal involvement. Cardiac involvement is seen in up to 45% of the patients, and although, pericardial involvement is the most common cardiac pathology of this rare disease, cardiac tamponade due to ECD has been very rarely reported. We describe a case of a patient found to have ECD with multi-organ involvement and small pericardial effusion, which progressed to cardiac tamponade despite treatment with interferon alpha." @default.
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- W2051289796 date "2014-04-23" @default.
- W2051289796 modified "2023-10-03" @default.
- W2051289796 title "Rapid progression to cardiac tamponade in Erdheim–Chester disease despite treatment with interferon alpha" @default.
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- W2051289796 doi "https://doi.org/10.3109/14397595.2014.905235" @default.
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