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1 From the Pulmonology Unit, Hôpital Bichat, Paris, France
2 From the Pathology Department, Hôpital Bichat, Paris, France
We report the case of a man with biopsy-proved pulmonary Langerhans' cell granulomatosis (histiocytosis X) and pulmonary precapillary hypertension. Pulmonary vascular resistances and mean pulmonary artery pressure decreased with corticosteroid therapy and dyspnea improved.
Key Words: Langerhans' cell granulomatosis pulmonary hypertension steroids
Submitted on October 10, 1995
Accepted on January 26, 1996
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