Long-term improvement during tadalafil therapy in a patient with pulmonary hypertension secondary to pulmonary Langerhans cell histiocytosis

Pulmonary arterial hypertension (PAH) secondary to pulmonary Langerhans cell histiocytosis (PLCH) is known to be a relatively common complication and is associated with a poor prognosis. However, the optimal therapeutic approach for these cases remains to be established. A 57-year-old man visited ou...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Respir Med Case Rep
Autors principals: Nemoto, Kenji, Oh-ishi, Shuji, Inui, Toshihide, Nakazawa, Mariko, Hyodo, Kentaro, Nakajima, Masayuki, Kanazawa, Jun, Miura, Yukiko, Takaku, Takio, Minami, Yuko, Hayashihara, Kenji, Saito, Takefumi, Kawabata, Yoshinori
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2016
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4913144/
https://ncbi.nlm.nih.gov/pubmed/27330952
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2016.04.008
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars