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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...
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| Udgivet i: | BMJ Case Rep |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMJ Publishing Group
2019
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| Fag: | |
| Online adgang: | 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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