Apical Hypertrophic Cardiomyopathy in an African American: A Case Presentation and Literature Review
نویسندگان
چکیده
We present a case of a patient with a two-month history of night sweats, nausea and vomiting, fatigue and shortness of breath on exertion as well as significant weight loss. Prior to arrival at our facility he was diagnosed with apical aneurism and was offered an evaluation with cardiac catheterization but the patient decided on a second opinion and thus came to our facility. The apical aneurism turned out to be apical variant hypertrophic cardiomyopathy, which is a common echocardiographic misinterpretation and thus necessitating additional imaging modalities such as cardiac MRI. We perform a comprehensive and up to date literature review of apical variant hypertrophic cardiomyopathy as it relates to epidemiology, diagnosis, prognosis and treatment as some variants portend poorer prognosis and it is often misdiagnosed on initial Echocardiography as described in our case presentation.
منابع مشابه
Apical Hypertrophic Cardiomyopathy in a Case with Chest Pain and Family History of Sudden Cardiac Death: A Case Report
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease, which is caused by a multitude of mutations in genes encoding proteins of the cardiac sarcomere (1). Apical hypertrophic cardiomyopathy (AHCM) is an uncommon type of HCM. The sudden cardiac death is less likely to occur in the patients inflicted with AHCM (2). Herein, we presented the case of a 29-year-old man ...
متن کاملHypertrophic non-obstructive apical cardiomyopathy. A case presentation and review of the literature.
A 20-year-old Coloured man gave a history of atypical chest pain, palpitations after strenuous exercise and a single episode of post-exertional presyncope. The diagnosis of hypertrophic non-obstructive apical cardiomyopathy (HNOAC) was established by means of electrocardiography, echocardiography (both M-mode and two-dimensional) and left ventricular cineangiography. This variant of hypertrophi...
متن کاملApical Hypertrophic Cardiomyopathy Among Non-Asians: A Case Series and Review of the Literature
Apical hypertrophic cardiomyopathy (AHCM) has been rarely described in the Western world. More recently, improved sensitivity of diagnostic modalities and increased diagnostic awareness have increased detection rates, suggesting that the prevalence outside of Asia may have been previously understated. Hallmark features of AHCM include deeply negative, "giant" T-wave inversions on electrocardiog...
متن کاملApical Hypertrophic Cardiomyopathy: A Case Report
Apical hypertrophic cardiomyopathy (ApHCM) is a rare variant of hypertrophic cardiomyopathy, characterized by a spade-like left ventricular cavity. A 58-year-old African-American female with past medical history of hypertension presented for evaluation of recurrent exertional chest tightness, palpitations and headache. Prior workup including multiple stress tests and angiogram was non-conclusiv...
متن کاملSubaortic and mid-ventricular obstructive hypertrophic cardiomyopathy with an apical Aneurysm: a case report
BACKGROUND Most patients with hypertrophic cardiomyopathy (HCM) have asymmetric septal hypertrophy and among them, 25% present dynamic subaortic obstruction. Apical HCM is unusual and mid-ventricular HCM is the most infrequent presentation, but both variants may be associated to an apical aneurysm. An even more rare presentation is the coexistence mid-ventricular and apical HCM. This case is a ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2016