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Screening for Hypertrophic Obstructive Cardiomyopathy in Patients With Panic Disorder: A Case Report
Thomas Bonitz1, Luke Scypinski1, Justin Chin2,1
1Medical Education, Lake Erie College of Osteopathic Medicine, Erie, USA.
Insights
Hypertrophic obstructive cardiomyopathy (HOCM) can mimic panic disorder symptoms. Early diagnosis through genetic screening is crucial for appropriate HOCM management and preventing sudden cardiac death.
Area of Science:
- Cardiology
- Genetics
- Psychiatry
Background:
- Hypertrophic obstructive cardiomyopathy (HOCM) is an inherited cardiovascular disease causing cardiac dysfunction.
- It presents with symptoms like dyspnea and exercise intolerance, potentially leading to sudden death.
- Panic disorder shares similar symptoms but requires different management.
Observation:
- A 56-year-old male with a history of panic disorder presented with palpitations, lightheadedness, and dyspnea.
- He was hospitalized for ventricular tachyarrhythmia, leading to an HOCM diagnosis.
- This case underscores symptom overlap between HOCM and panic disorder.
Findings:
- The patient's symptoms were initially attributed to panic disorder.
- Further investigation revealed underlying HOCM, complicated by ventricular tachyarrhythmia.
- This highlights diagnostic challenges when conditions present similarly.
Implications:
- Emphasizes the need for thorough patient history and chronic symptom follow-up.
- Suggests considering genetic screening for HOCM in patients with panic disorder.
- Underscores the critical differences in HOCM and panic disorder treatment and precautions.
Abstract:
Hypertrophic obstructive cardiomyopathy (HOCM) is a cardiovascular disease that is widely recognized as an important cause of various cardiovascular pathologies. Passed through an autosomal dominant inheritance pattern, mutations can result in cardiac dysfunction that can manifest in dyspnea, exercise intolerance, and sudden death. Panic disorder can present similarly to HOCM; however, precautions and treatment differ significantly. Here, we present a case of a 56-year-old male with a history of panic disorder who presented to the emergency department with recurrent episodes of palpitations, lightheadedness, and dyspnea, and who was subsequently hospitalized due to new ventricular tachyarrhythmia and diagnosed with HOCM. This case highlights the importance of detailed history taking, follow-up of chronic symptoms, and consideration of genetic screening for HOCM in patients with panic disorder.
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