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A previously healthy 38-year-old man with no history of cardiovascular disease presented with symptoms of upper respiratory tract infection, acute chest pain, inferior ST-elevation on ECG and a troponin I >60 μg/L (normal <0.04 μg/L). Emergency coronary angiography demonstrated normal coronary arteries. ECG showed moderate impairment of LV systolic function, inferoposterior wall hypokinesis and severe concentric LV hypertrophy (septum up to 22 mm) with a speckled appearance. A cardiovascular MR (CMR) study was requested to further evaluate the cause of LV hypertrophy (figure 1).
Based on these CMR images (and online supplementary video), the most likely diagnosis is:
Hypertrophic cardiomyopathy (HCM)
CMR showed mild global LV hypokinesis (EF 62%) and severe concentric hypertrophy (wall thickness 20 mm, LV mass 250 g). On T2-weighted imaging, there was a significant increase in global myocardial signal intensity (SI) when compared with adjacent skeletal muscle (T2 SI ratio 2.8; normal <2.0), demonstrating global myocardial oedema. On T1-maps,1 green areas denote normal myocardium (normal T1 value 962±25 ms at 1.5 Tesla),2 whereas red indicates areas of myocardium with a significant increase in T1 value of >990 ms, consistent with acute myocardial oedema.3 In this patient, there was a significant (∼10%) increase in mean myocardial T1 (1054±62 ms). Late gadolinium enhancement (LGE) imaging showed a predominantly non-ischemic pattern of myocyte necrosis, with diffuse hazy enhancement throughout the LV and areas of subepicardial and mid-wall enhancement in a non-coronary distribution, consistent with myocarditis. This is in contrast to acute myocardial infarction, which typically shows an area of LGE with subendocardial involvement and variable transmural extent in the distribution of a single coronary artery.
The correct answer is (B). Extensive acute myocarditis was most likely, with severe oedema causing a significant increase in wall thickness and mass. However, given the severe LV hypertrophy (20 mm), background HCM with concomitant myocarditis was a possibility. A follow-up CMR was important in this case which showed resolution of the oedema (global myocardial T2 SI ratio 1.5), with normalisation of the LV mass (102 g), wall thickness (8–12 mm) and mean myocardial T1 (964±72 ms). There was also significant reduction in the areas of LGE. Normalisation of the massive changes at presentation in follow-up allowed exclusion of HCM and amyloidosis. Cardiac amyloidosis was also less likely as atrial sizes were normal without LGE, and LGE images typically show diffuse, mostly subendocardial enhancement in the LV with dark blood pool (due to binding of the gadolinium contrast to the amyloid protein); cardiac amyloidosis also shows a much higher increase (∼19%) in mean myocardial T1 (1140±61 ms).4 Anderson–Fabry disease is a lysosomal storage disease due to X linked recessive deficiency of the enzyme α-galactosidase, which leads to accumulation of glycosphingolipid within lysosomes. It typically shows moderate-to-severe concentric hypertrophy, mid-wall LGE in the basal inferolateral wall and low myocardial T1 values (882±47 ms).5 Athlete's heart does not present with features of oedema, and the degree of physiologic hypertrophy is mild (13–15 mm in wall thickness), which normalises with detraining.
Review history and Supplementary material
Contributors All authors gave final approval of the version published. Additionally, VMF was involved in the conception of the manuscript, acquisition of the images, analysis and interpretaion of data and drafting the article; SKP was involved in data analysis, design of the threshold-based colour scale for coloured T1-maps and revision of the article and SF was involved in the conception and revision of the article. TDK and SN were involved in the conception of the article, interpretation of data and revision of the article for important intellectual content.
Competing interests VMF and SKP are funded by the Oxford National Institute for Health Research Biomedical Research Centre Programme. VMF received funding from the Alberta Innovates Health Solutions Clinical Fellowship and the University of Oxford Clarendon Fund Scholarship. SN acknowledges support from the British Heart Foundation Centre of Research Excellence, Oxford. The authors acknowledge support by the Oxford National Institute for Health Research Biomedical Research Centre Programme. Dr. Piechnik has a patent Sh-MOLLI cardiac gated T1 mapping of T1 licensed to Siemens, and a patent colour map design method for immediate assessment of the deviation from established normal population statistics and its application to cardiovascular T1 mapping images pending.
Patient consent Obtained.
Provenance and peer review Not commissioned; internally peer reviewed.
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