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Spontaneous idiopathic pulmonary artery dissection with ST segment elevation in Leads aVR and V1

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dc.creator KARADEM, Kadir Burhan
dc.creator Cora, Ahmet Rifki
dc.creator Celik, Ersin
dc.date 2022-01-01T00:00:00Z
dc.date.accessioned 2022-05-10T11:20:19Z
dc.date.available 2022-05-10T11:20:19Z
dc.identifier 8c5fddd1-d107-45d6-a45b-732ed84cee80
dc.identifier 10.5606/tgkdc.dergisi.2022.2079
dc.identifier https://avesis.sdu.edu.tr/publication/details/8c5fddd1-d107-45d6-a45b-732ed84cee80/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/96777
dc.description Pulmonary artery dissection is a rare condition that often occurs on the basis of pulmonary arterial hypertension and causes complications such as cardiogenic shock and sudden death. Additionally, this condition can be idiopathic. A 59-year-old male patient with no previous history of disease presented to our clinic with chest pain and shortness of breath. Coronary arteries were normal on coronary angiography in the patient who had a positive troponin test result and ST segment elevation in leads V1, V2, V3 and aVR. Pulmonary embolism was suspected in the patient whose condition worsened. Pulmonary artery dissection was diagnosed via the contrast-enhanced computed tomography and sudden cardiac death occurred. In conclusion, pulmonary artery dissection may cause aVR segment elevation on electrocardiography.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Spontaneous idiopathic pulmonary artery dissection with ST segment elevation in Leads aVR and V1
dc.type info:eu-repo/semantics/article


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