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Journal of Cardiovascular Imaging logoLink to Journal of Cardiovascular Imaging
. 2019 Feb 13;27(2):156–157. doi: 10.4250/jcvi.2019.27.e15

A Case of Reversible but Highly Vulnerable Adriamycin-induced Cardiomyopathy: A Multi-modality Imaging Approach

Mi-Hyang Jung 1,✉, Jung Im Jung 2, Sang Min Park 1, Ho-Joong Youn 3, Kyung-Soon Hong 1
PMCID: PMC6470071  PMID: 30993953

A 63-year-old woman presented with exertional dyspnea. She had received 6 cycles of adriamycin-based chemotherapy 5 years prior and an additional 6 cycles of the same regimen due to cancer metastasis. Treatments were completed 3 weeks before onset of dyspnea. The cumulative dose of adriamycin was 563 mg/m2. Her B-type natriuretic peptide level was 4,116 pg/mL (reference: < 100 pg/mL), and transthoracic echocardiography revealed severe dysfunction [left ventricular ejection fraction (LVEF) 33%, global longitudinal strain (GLS) −8.3%]. We started heart failure medications, and her symptoms improved. Follow-up echocardiography showed gradual improvement: LVEF changed from 33% to 52% to 61% (Movie 1, 2, 3) and GLS from −8.3% to −13.0% to −17.1% (Figures 1A-C). Subsequently, beta-blocker dose was halved due to low blood pressure and no further complaints of dyspnea. One month later, however, she presented at an emergency department with resting dyspnea with decreased LVEF of 33%. After the stabilization period, we performed echocardiography; surprisingly, the LVEF again recovered to 58.6% and GLS to −17.5%. Cardiac magnetic resonance imaging (3T, Verio, Siemens, Enlangen, Germany) showed elevated native T1 value (1,394–1,411 ms, reference: 1,278 ± 30 ms), T2 value (55–59 ms, reference: 40.5 ± 2.5 ms), and extracellular volume fraction (ECV, 32.5-33.3%, reference: 27.4 ± 2.4%), although we did not detect late gadolinium enhancement (Figures 1D-F). These findings suggest diffuse interstitial fibrosis combined with edema and inflammation, which might explain the myocardial vulnerability. Consistent with recent studies,1),2),3),4) our case shows the usefulness of multi-modality imaging for evaluation of myocardial vulnerability.

Figure 1. (A) Global longitudinal strain (GLS) at initial presentation (-8.3%). (B) GLS after 3 months of heart failure management (-13.0%). (C) GLS after 6 months of heart failure management (-17.1%). (D) Native T1 mapping of left ventricle (LV) (1,394 msec). (E) Post-contrast T1 mapping of LV (453 msec); extracellular volume was then calculated (32.5%). (F) Late gadolinium enhancement imaging.

Figure 1

Footnotes

Conflict of Interest: The authors have no financial conflicts of interest.

SUPPLEMENTARY MATERIALS

Movie 1

Initial echocardiography.

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Movie 2

Follow-up echocardiography performed after 3 months of heart failure management.

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Movie 3

Follow-up echocardiography performed after 6 months of heart failure management.

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References

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Associated Data

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Supplementary Materials

Movie 1

Initial echocardiography.

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Movie 2

Follow-up echocardiography performed after 3 months of heart failure management.

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Movie 3

Follow-up echocardiography performed after 6 months of heart failure management.

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