Pulmonary hypertension causes: Difference between revisions
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Etiologies of Pulmonary Hypertension organized under the classification of pulmonary hypertension put by the World Health Organization in 1998 | {{CMG}} | ||
'''Etiologies of Pulmonary Hypertension organized under the classification of pulmonary hypertension put by the World Health Organization in 1998''' | |||
==Pulmonary Aterial Hypertension== | ==Pulmonary Aterial Hypertension== |
Revision as of 21:14, 7 September 2011
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Etiologies of Pulmonary Hypertension organized under the classification of pulmonary hypertension put by the World Health Organization in 1998
Pulmonary Aterial Hypertension
- Idiopathic PAH
- Heritable( BMPR2,ALK-1,Endogin...)
- Drug and toxin induced.
- Connective tissue diseases
- HIV
- Portal Hypertension
- Congenital heart diseases
- Schistosomiasis
- Chronic hemolytic anemia.
- Persistent Pulmonary Hypertension of the newborn
Pulmonary Venous Hypertension or pulmonary hypertension owing to left heart disease
- Systolic Dysfunction.
- Diastolic dysfunction.
- Valvular disease.
Pulmonary Hypertension associated with disorders of the respiratory system and/or Hypoxemia
- Chronic Obstructive Pulmonary Disease.
- Interstitial Lung Disease
- Pulmonary diseases with mixed restrictive and obstructive patterns.
- Obstructive sleep apnea.
- High Altitude(chronically).
- Developmental abnormalities.
Pulmonary Hypertension due to chronic thrombotic and/or embolic disease
Pulmonary Hypertension due to disorders directly affecting the pulmonary vasculature
- Hematologic disorders: Myeloproliferative disorders,splenectomy,polycythemia vera.
- Systemic disorders: Sarcoidosis,Langerhan cell Histiocytosis, Neurofibromatosis, Vasculitis.
- Metabolic disorders: Glycogen storage diseases, Gaucher disease, Thyroid disorders.
- Miscellaneous: Tumor obstruction, Fibrosing mediastinitis, chronic renal failure on dialysis.