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- Raymond J Foley and Mark L Metersky.
- Division of Pulmonary/Critical Care Medicine, University of Connecticut School of Medicine, Farmington, Conn., USA. rfoley@uchc.edu
- Respiration. 2008 Jan 1; 75 (2): 211-4.
AbstractSarcoidosis is a systemic granulomatous disease of unknown etiology, in which the lungs and intrathoracic lymph nodes are predominant sites of involvement. Pulmonary hypertension is a known complication of sarcoidosis. Treatment of sarcoidosis-associated pulmonary hypertension has traditionally focused on the initiation of systemic corticosteroids, but has had inconsistent results. We present a patient with sarcoidosis-associated pulmonary hypertension who achieved substantial clinical improvement with the dual endothelin receptor antagonist bosentan.Copyright (c) 2008 S. Karger AG, Basel
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