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1.
Eur Heart J Case Rep ; 3(2)2019 Jun 01.
Article in English | MEDLINE | ID: mdl-31449636

ABSTRACT

BACKGROUND: The increasing number of transcatheter aortic valve implantation (TAVI) in the last few years has unveiled a unique set of events and complications that need prompt recognition and management in order to improve patient outcomes, often involving a multidisciplinary team. CASE SUMMARY: We present a case of a 86-year-old woman with symptomatic severe aortic stenosis that underwent a TAVI and, in the post-procedure period, presented with acute abundant haematemesis, haemodynamic instability, and haemoglobin drop. The diagnosis of acute necrotizing oesophagitis (ANE) was made by upper gastrointestinal endoscopy. DISCUSSION: Acute necrotizing oesophagitis is a rare entity caused usually by an ischaemic insult in the presence of predisposing factors; it has a high rate of complications and mortality. To the best of our knowledge, this is the first clinical case report to describe the occurrence of ANE as a possible complication of TAVI and is also an example of the importance of the multidisciplinary approach of these complex patients, which extends even beyond the concept of Heart Team.

3.
Rev Port Cardiol ; 33(3): 177.e1-6, 2014 Mar.
Article in English, Portuguese | MEDLINE | ID: mdl-24684896

ABSTRACT

Pheochromocytoma is a tumor originating from chromaffin tissue. It commonly presents with symptoms and signs of catecholamine excess, such as hypertension, tachycardia, headache and sweating. Cardiovascular manifestations include catecholamine-induced cardiomyopathy, which may present as severe left ventricular dysfunction and congestive heart failure. We report a case of pheochromocytoma which was diagnosed following investigation of dilated cardiomyopathy. We highlight the dramatic symptomatic improvement and reversal of cardiomyopathy, with recovery of left ventricular function after treatment.


Subject(s)
Adrenal Gland Neoplasms/complications , Cardiomyopathy, Dilated/etiology , Pheochromocytoma/complications , Adrenal Gland Neoplasms/blood , Adult , Cardiomyopathy, Dilated/blood , Catecholamines/blood , Humans , Male , Pheochromocytoma/blood
4.
Rev Port Cardiol ; 29(12): 1879-88, 2010 Dec.
Article in English, Portuguese | MEDLINE | ID: mdl-21428143

ABSTRACT

Coronary vasospasm is one cause of chest pain in patients with acute myocarditis. This is a rare association, with few cases reported in the literature. The authors describe a case of acute myocarditis in which presentation mimicked acute myocardial infarction. During hospitalization severe angina recurred twice, accompanied by transient ST-segment elevation in different locations. The hypothesis of coronary vasospasm is discussed. The role of cardiac magnetic resonance imaging in this context is highlighted.


Subject(s)
Coronary Vasospasm/complications , Myocarditis/complications , Acute Disease , Adult , Humans , Male
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