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Central airway compression by massively dilated pulmonary artery in a patient with pulmonary arterial hypertension: a rare entity
Patients with pulmonary arterial hypertension (PAH) usually die from progressive right ventricular failure. Mechanical complications due to pulmonary artery (PA) enlargement are rare and include tracheobronchial and left main coronary artery compression, and PA dissection. A 62-year-old female with...
Gorde:
| Argitaratua izan da: | BMJ Case Rep |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BMJ Publishing Group
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6887364/ https://ncbi.nlm.nih.gov/pubmed/31772136 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-232468 |
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