Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2006;113:e842-e843
doi: 10.1161/CIRCULATIONAHA.104.532481
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fenster, B. E.
Right arrow Articles by Yang, P. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fenster, B. E.
Right arrow Articles by Yang, P. C.
Related Collections
Right arrow Congestive
Right arrow Imaging
Right arrow CT and MRI
Right arrowRelated Article

(Circulation. 2006;113:e842-e843.)
© 2006 American Heart Association, Inc.


Images in Cardiovascular Medicine

Cardiac Magnetic Resonance Imaging for Myocarditis

Effective Use in Medical Decision Making

Brett E. Fenster, MD; Frandics P. Chan, MD, PhD; Hannah A. Valentine, MD; Eugene Yang, MD; Michael V. McConnell, MD; Gerald J. Berry, MD; Phillip C. Yang, MD

From the Division of Cardiovascular Medicine (B.E.F., H.A.V., E.Y., M.V.M., P.C.Y.), Department of Radiology (F.P.C.), and Department of Pathology (G.J.B.), Stanford University, Stanford, Calif.

Correspondence to B.E. Fenster, MD, Stanford University, Division of Cardiovascular Medicine, 300 Pasteur Dr, Falk/CVRC, CV 187, Stanford, CA 94305. E-mail bfenster{at}cvmed.stanford.edu

A 19-year-old man presented with new onset fatigue and dyspnea. The results of the physical examination were unremarkable. ECG was unremarkable for any ischemic changes. Echocardiography demonstrated severe global hypokinesis with an ejection fraction of 15% to 25%. Laboratory workup was remarkable for a troponin I level of 1.56, brain natriuretic peptide of 2249, white blood cell count of 32 000, C-reactive protein of 13, and creatine kinase of 156. Cardiac catheterization demonstrated no significant coronary artery disease, a pulmonary capillary wedge pressure of 3 mm Hg, and cardiac index of 2.7. Right ventricular biopsies were negative for myocarditis. Suspecting myocarditis, we performed cardiac magnetic resonance imaging (MRI), which demonstrated severe global left ventricular dysfunction (Figure, A and B, and Movie I) with focal delayed enhancement in the distal lateral wall suggestive of myocarditis (Figure, C and D). A left ventricular septal biopsy confirmed the diagnosis (Figure, I and J). We initiated immunosuppressive therapy consisting of intravenous steroids and cyclosporine. Two weeks later, repeat cardiac MRI revealed a normalized left ventricular function with an ejection fraction of 55% (Figure, G and H, and Movie II) and resolution of the lateral wall delayed enhancement (Figure, E and F, arrows). Our experience suggests that cardiac MRI can noninvasively detect myocarditis and that it may be particularly useful in deciding to proceed to left ventricular biopsy when right ventricular biopsies are negative and a high clinical suspicion for myocarditis remains.


Figure 1175606
View larger version (166K):
[in this window]
[in a new window]
 
Four-chamber steady-state free precession imaging in end diastole (A) and end systole (B) performed on presentation, demonstrating severe left ventricular dysfunction (time to repetition, 3.8 ms; time to echo 1.6 ms; field of view, 36 cm; slice thickness, 8 mm). Four-chamber (C) and short-axis (SAX) (D) views of inversion recovery myocardial-suppressed gradient-recalled echo sequence after administration of 0.2 mmol/L per kg of gadolinium (time to inversion, 200 ms for 4 chamber, 240 ms for SAX; time to repetition, 7.1 ms; time to echo, 3.1 ms; field of view, 36 cm; slice thickness, 10 mm; 10- to 20-minute contrast delay) demonstrating focal delayed enhancement in the distal lateral wall (arrows). Identical 4-chamber steady-state free precession end diastole (G) and end systole (H) images and delayed enhancement 4-chamber (E) and SAX (F) sequences performed 2 weeks later showing normalized left ventricle function and resolution of focal delayed enhancement (arrows). I and J, Hematoxylin and eosin-stained left ventricular biopsy demonstrating lymphocytic infiltrate and myocyte necrosis.


*    Acknowledgments
 
Sources of Funding

Dr McConnell has received a research grant from GE Healthcare, Inc. Dr Yang received a grant from Stanford University and support from GE Medical Systems for magnetic resonance system research.

Disclosures

None.


*    Footnotes
 
The online-only Data Supplement, which contains 2 movies, can be found at http://circ.ahajournals.org/cgi/content/full/113/22/e842/DC1.


Related Article:

Issue Highlights
Circulation 2006 113: 2565. [Full Text]




This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fenster, B. E.
Right arrow Articles by Yang, P. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fenster, B. E.
Right arrow Articles by Yang, P. C.
Related Collections
Right arrow Congestive
Right arrow Imaging
Right arrow CT and MRI
Right arrowRelated Article