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Echocardiographic and Clinical Characteristics of Pulmonary Hypertension Complicating Pulmonary Langerhans Cell Histiocytosis

✍ Scribed by Chaowalit, Nithima; Pellikka, Patricia A.; Decker, Paul A.; Aubry, Marie-Christine; Krowka, Michael J.; Ryu, Jay H.; Vassallo, Robert

Book ID
123588869
Publisher
Mayo Clinic
Year
2004
Tongue
English
Weight
109 KB
Volume
79
Category
Article
ISSN
0025-6196

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## Abstract ## Background In Langerhans cell histiocytosis (LCH) pulmonary involvement, which is often initially asymptomatic, may contribute to significant morbidity and mortality. To determine the long‐term prognosis, a cross‐sectional study was undertaken. ## Procedure Forty‐one patients with