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Published on: September 25, 2017
Left ventricular hypertrophy diagnosed after a stroke: a case report
Wilfred Ifeanyi Umeojiako1, Ritesh Kanyal2
1Medway Maritime Hospital, Windmill road, Gillingham, ME7 5NY, UK. wilfred.umeojiako@nhs.net.
Insights
Stroke can unmask left ventricular hypertrophy, a key indicator of apical hypertrophic cardiomyopathy. This case highlights electrocardiogram changes appearing days after a stroke, emphasizing the need for differential diagnosis in hypertrophic cardiomyopathy.
Area of Science:
- Cardiology
- Neurology
- Medical Imaging
Background:
- Stroke is a known complication of hypertrophic cardiomyopathy.
- This case presents a unique electrocardiogram (ECG) evolution in a patient with hypertrophic cardiomyopathy.
Observation:
- An 83-year-old woman with atrial fibrillation and hypertension experienced a stroke.
- Post-stroke ECG revealed marked left ventricular hypertrophy (LVH) with apical hypertrophic cardiomyopathy, not present pre-stroke.
- Cardiovascular magnetic resonance imaging confirmed apical hypertrophic cardiomyopathy.
Findings:
- ECG diagnosis of LVH using Sokolow-Lyon indices was crucial.
- LVH manifested days after the stroke, with unclear underlying mechanisms.
- Apical hypertrophic cardiomyopathy was diagnosed based on ECG and imaging findings.
Implications:
- Consider hypertrophic cardiomyopathy in patients with ECG criteria for LVH.
- Cardiovascular magnetic resonance imaging is vital for diagnosing LVH causes.
- Family screening is recommended for new hypertrophic cardiomyopathy diagnoses.
Background:
Stroke is a recognized clinical course of hypertrophic cardiomyopathy. This interesting case showed notable difference on the electrocardiogram of a patient 4 months prior to suffering a stroke and 10 days after suffering a stroke. The pre-stroke electrocardiogram showed atrial fibrillation with a narrow QRS complex, while the post-stroke electrocardiogram showed marked left ventricular hypertrophy. Left ventricular hypertrophy was diagnosed using the Sokolow-Lyon indices. The development of left ventricular hypertrophy a few days after suffering a stroke has not previously been reported.
Case Presentation:
An 83-year-old white British woman with a background history of permanent atrial fibrillation, hypertension, and previous stroke attended the emergency department with a 2-day history of exertional dyspnea, and chest tightness. On examination, she had bibasal crepitations with a systolic murmur loudest at the apex. In-patient investigations include an electrocardiogram, blood tests, chest X-ray, contrast echocardiogram, coronary angiogram, and cardiovascular magnetic resonance imaging. An electrocardiogram showed atrial fibrillation, with inferolateral T wave inversion, and left ventricular hypertrophy. A chest X-ray showed features consistent with pulmonary edema. A contrast echocardiogram showed marked hypertrophy of the mid to apical left ventricle, appearance consistent with apical hypertrophic cardiomyopathy. Coronary angiography showed eccentric shelf-type plaque with non-flow-limiting stenosis in the left coronary artery main stem. Cardiovascular magnetic resonance imaging reported findings highly suggestive of apical hypertrophic cardiomyopathy. Our patient was treated and discharged on rivaroxaban, bisoprolol, and atorvastatin with a follow-up in the cardiomyopathy outpatient clinic.
Conclusions:
Electrocardiogram diagnosis of left ventricular hypertrophy led to the diagnosis of apical hypertrophic cardiomyopathy in this patient. Left ventricular hypertrophy was only evident a few days after our patient suffered a stroke. The underlying mechanisms responsible for this remain unclear. Furthermore, differential diagnosis of hypertrophic cardiomyopathy should be considered in people with electrocardiogram criteria for left ventricular hypertrophy. Cardiovascular magnetic resonance imaging is an important diagnostic tool in identifying causes of left ventricular hypertrophy. Family screening should be recommended in patients with new diagnosis of hypertrophic cardiomyopathy.
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