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An unexpected cause of hypertrophic myocardium.

Mathew GL, Vassiliou VS, Malley T, Symmonds K, Alpendurada F - Oxf Med Case Reports (2015)

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Affiliation: CMR Unit , Royal Brompton Hospital , London , UK.

No MeSH data available.


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(a) A hypertrophic myocardium with mildly dilated atria. (b) Diffuse enhancement associated with a relatively dark blood pool (difficult ‘ing’) of the myocardium, typical of cardiac amyloid.
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OMV029F2: (a) A hypertrophic myocardium with mildly dilated atria. (b) Diffuse enhancement associated with a relatively dark blood pool (difficult ‘ing’) of the myocardium, typical of cardiac amyloid.

Mentions: Initial CMR imaging for anatomy and function demonstrated normal ventricular size and mildly impaired systolic function (ejection fraction = 50%, normal >55%) with no significant valvular pathology. There was asymmetrical septal hypertrophy measuring 16 mm (normal <13 mm) in the basal septum versus 9 mm in the lateral wall at the same level with significantly elevated left ventricular mass at 241 g (Fig. 2a). There was no systolic anterior motion of the mitral valve or left ventricular outflow tract obstruction at rest. Both atria were slightly enlarged, the left atrium measuring 35 cm2 and the right atrium measuring 36 cm2. To identify the etiology of hypertrophy, conventional late gadolinium enhancement (Fig. 2b) was undertaken alongside novel native T1 mapping sequences (Fig. 3 and Supplementary Videos 1 and 2). Acquisition of late gadolinium images was technically challenging, giving the impression of diffuse enhancement associated with a relatively dark blood pool, both of which are suspicious of amyloid infiltration of the heart [1]. The native T1 maps showed an elevated septal T1 relaxation time (1148 ms, normal <1050 ms), supporting the initial impression of cardiac amyloid and further suggesting that this was most likely due to light chain deposition (AL amyloid) [2]. AL amyloid was subsequently confirmed by serum free light chain immunoassay and bone marrow trephine biopsy.Figure 2:


An unexpected cause of hypertrophic myocardium.

Mathew GL, Vassiliou VS, Malley T, Symmonds K, Alpendurada F - Oxf Med Case Reports (2015)

(a) A hypertrophic myocardium with mildly dilated atria. (b) Diffuse enhancement associated with a relatively dark blood pool (difficult ‘ing’) of the myocardium, typical of cardiac amyloid.
© Copyright Policy - creative-commons
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC4664860&req=5

OMV029F2: (a) A hypertrophic myocardium with mildly dilated atria. (b) Diffuse enhancement associated with a relatively dark blood pool (difficult ‘ing’) of the myocardium, typical of cardiac amyloid.
Mentions: Initial CMR imaging for anatomy and function demonstrated normal ventricular size and mildly impaired systolic function (ejection fraction = 50%, normal >55%) with no significant valvular pathology. There was asymmetrical septal hypertrophy measuring 16 mm (normal <13 mm) in the basal septum versus 9 mm in the lateral wall at the same level with significantly elevated left ventricular mass at 241 g (Fig. 2a). There was no systolic anterior motion of the mitral valve or left ventricular outflow tract obstruction at rest. Both atria were slightly enlarged, the left atrium measuring 35 cm2 and the right atrium measuring 36 cm2. To identify the etiology of hypertrophy, conventional late gadolinium enhancement (Fig. 2b) was undertaken alongside novel native T1 mapping sequences (Fig. 3 and Supplementary Videos 1 and 2). Acquisition of late gadolinium images was technically challenging, giving the impression of diffuse enhancement associated with a relatively dark blood pool, both of which are suspicious of amyloid infiltration of the heart [1]. The native T1 maps showed an elevated septal T1 relaxation time (1148 ms, normal <1050 ms), supporting the initial impression of cardiac amyloid and further suggesting that this was most likely due to light chain deposition (AL amyloid) [2]. AL amyloid was subsequently confirmed by serum free light chain immunoassay and bone marrow trephine biopsy.Figure 2:

View Article: PubMed Central - HTML - PubMed

Affiliation: CMR Unit , Royal Brompton Hospital , London , UK.

No MeSH data available.


Related in: MedlinePlus