Dramatic and sustained responsiveness of pulmonary Langerhans cell histiocytosis-associated pulmonary hypertension to vasodilator therapy

Pulmonary Langerhans cell histiocytosis (PLCH) is an uncommon diffuse lung disease characterized by the abnormal accumulation of Langerhans' cells around small airways and other distal lung compartments. Although pulmonary hypertension (PH) is a frequent complication of PLCH, the role of advanc...

Descripción completa

Detalles Bibliográficos
Autores principales: May, Adam, Kane, Garvan, Yi, Eunhee, Frantz, Robert, Vassallo, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356044/
https://www.ncbi.nlm.nih.gov/pubmed/26029568
http://dx.doi.org/10.1016/j.rmcr.2014.11.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356044/
https://www.ncbi.nlm.nih.gov/pubmed/26029568
http://dx.doi.org/10.1016/j.rmcr.2014.11.005

Ejemplares similares