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1.
Am J Med ; 135(4): 517-523, 2022 04.
Article in English | MEDLINE | ID: mdl-34813739

ABSTRACT

BACKGROUND: The incidence of precordial T changes has been described in athletes and in specific populations, while the etiology in a large patient population admitted to the hospital has not previously been reported. METHODS: All electrocardiograms (ECGs) read by the same physician with new (compared to prior ECGs) or presumed new (no prior ECGs) precordial T wave inversions of >1 mm (0.1 mV) in multiple precordial leads were retrospectively reviewed and various ECG, patient-related, and imaging parameters assessed. A total of 226 patients and their ECGs were initially selected for analysis. Of these, 35 were eliminated leaving 191 for the final analysis. RESULTS: Patients and their ECGs were divided into 5 groups based on diagnosis and incidence including Wellens syndrome, takotsubo, type 2 myocardial infarction, other (including multiple diagnoses), and unknown. Although subtle differences including number of T inversion leads, depth of T waves, QTc intervals, and other variables were present between some groups, diagnosis in individual cases required appropriate clinical, laboratory, or imaging studies. For example, although Wellens syndrome was identified in <20% of cases, a presenting history of chest discomfort with precordial T changes either on the admission or next-day ECG was highly sensitive and specific for this diagnosis. In some cases, type 2 myocardial infarction can also have a Wellens-like ECG phenotype without significant left anterior descending disease. CONCLUSIONS: Precordial T wave changes in hospitalized patients have various etiologies, and in individual cases, the changes on the ECG alone cannot easily distinguish the presumptive diagnosis and additional data are required.


Subject(s)
Anterior Wall Myocardial Infarction , Thoracic Wall , Arrhythmias, Cardiac , Electrocardiography/methods , Humans , Retrospective Studies
2.
Methodist Debakey Cardiovasc J ; 17(2): 157-160, 2021.
Article in English | MEDLINE | ID: mdl-34326936

ABSTRACT

Aorto-right ventricular outflow tract fistulas typically occur secondary to trauma, infective endocarditis, and sinus of Valsalva aneurysm rupture. We describe an unusual case of a spontaneous aorto-right ventricular outflow tract fistula in the absence of such findings, instead forming secondary to a complicating supracristal ventricular septal defect and leading to dilated cardiomyopathy.


Subject(s)
Aortic Aneurysm , Fistula , Heart Septal Defects, Ventricular , Sinus of Valsalva , Aortic Aneurysm/diagnostic imaging , Aortic Aneurysm/etiology , Aortic Aneurysm/surgery , Fistula/diagnostic imaging , Fistula/etiology , Fistula/surgery , Heart Septal Defects, Ventricular/diagnostic imaging , Heart Septal Defects, Ventricular/surgery , Heart Ventricles/diagnostic imaging , Heart Ventricles/surgery , Humans , Sinus of Valsalva/diagnostic imaging , Sinus of Valsalva/surgery
3.
Clin Case Rep ; 6(5): 961-962, 2018 May.
Article in English | MEDLINE | ID: mdl-29744101

ABSTRACT

Renal cell carcinoma is a highly malignant neoplasm. Metastasis to the pancreas and gastrointestinal tract is rare. In this case report, we show images of metastatic renal cell carcinoma to the upper gastrointestinal tract in a patient who presented with melena.

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