Hypertrophic cardiomyopathy with anteriorly directed mitral regurgitation is a red flag for concomitant pathology: a case report

Author:

Somma Vincenzo1ORCID,Raman Jaishankar2,Fitzpatrick Leigh3,Prior David145,Paratz Elizabeth1567ORCID

Affiliation:

1. Department of Cardiology, St Vincent’s Hospital Melbourne , 41 Victoria Parade, Fitzroy, VIC 3065 , Australia

2. Department of Cardiothoracic Surgery, St Vincent’s Hospital Melbourne , 41 Victoria Parade, Fitzroy, VIC 3065 , Australia

3. Department of Intensive Care, Albury-Wodonga Health , 201 Borella Road, East Albury, NSW 2640 , Australia

4. Department of Cardiology, Albury-Wodonga Health , Vermont St, Wodonga, VIC 3690 , Australia

5. Faculty of Medicine, Dentistry and Health Sciences, Melbourne University , Grattan St, Parkville, VIC 3000 , Australia

6. HEART Research Lab, St Vincent’s Institute of Medical Research , 9 Princes St Fitzroy, Fitzroy, VIC 3065 , Australia

7. Department of Sports Cardiology, Baker Heart and Diabetes Institute , 75 Commercial Rd, Prahran, VIC 3181 , Australia

Abstract

Abstract Background Hypertrophic cardiomyopathy (HCM) is often linked to systolic anterior motion (SAM) of the mitral valve, typically resulting in a posteriorly directed mitral regurgitation (MR) jet. An anteriorly directed MR jet suggests additional mitral valve pathology that may not be resolved by myectomy alone. Case summary A 58-year-old construction worker with no significant medical history experienced a syncopal event and was admitted to the emergency department with acute pulmonary oedema. A systolic murmur was investigated with a trans-thoracic echocardiogram that revealed severe MR with an unusual anteriorly directed MR jet and a possible flail segment of the posterior leaflet. This finding was further characterized with a trans-oesophageal echocardiogram that revealed severe asymmetric septal hypertrophy with SAM of the mitral valve, severe mitral regurgitation into a dilated left atrium with pulmonary vein flow reversal not caused by HCM-associated SAM, and a markedly abnormal mitral valve with flail and prolapse. The patient underwent successful cardiac surgery, including mitral valve repair and septal myectomy. The patient’s recovery was uneventful, allowing for a return to work within a month post-surgery. Discussion The anteriorly directed MR jet served as a red flag, leading to the discovery of an independent mitral valve pathology that required surgical intervention beyond the expected treatment for SAM-associated HCM. This case highlights the complexity of assessing MR in patients with HCM and underscores the importance of characterizing MR jet direction in diagnosing additional mitral valve diseases.

Funder

Wilma Beswick Senior Research Fellowship

Melbourne University

Publisher

Oxford University Press (OUP)

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