JACC: CARDIOVASCULAR IMAGING
VOL. 7, NO. 9, 2014
ª 2014 BY THE AMERICAN COLLEGE OF CARDIOLOGY FOUNDATION
ISSN 1936-878X/$36.00
PUBLISHED BY ELSEVIER INC.
http://dx.doi.org/10.1016/j.jcmg.2014.05.009
Value of CMR for the Differential Diagnosis of Cardiac Masses Pablo Pazos-López, MD,*y Eduardo Pozo, MD,* Maria E. Siqueira, MD,* Inés García-Lunar, MD,*y Matthew Cham, MD,* Adam Jacobi, MD,* Frank Macaluso, BS,* Valentín Fuster, MD, PHD,*y Jagat Narula, MD, PHD,* Javier Sanz, MD*
JACC: CARDIOVASCULAR IMAGING CME CME Editor: Ragavendra R. Baliga, MD
5. Claim your CME credit and receive your certificate electronically by following the instructions given at the conclusion of the activity.
This article has been selected as this issue’s CME activity, available online at http://imaging.onlinejacc.org by selecting the CME tab on the top
CME Objective for This Article: After reading this article the reader
navigation bar.
should: 1) recognize the additive value of cardiac MRI for the differential diagnosis of cardiac masses; 2) recall cardiac MRI specific
Accreditation and Designation Statement The American College of Cardiology Foundation (ACCF) is accredited by
features that are valuable to differentiate a thrombus from a tumor; and 3) recall cardiac MRI specific features that may be helpful to differentiate a benign from malignant neoplasm.
the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians. The ACCF designates this Journal-based CME activity for a maximum of 1 AMA PRA Category 1 Credit(s). Physicians should only claim credit commensurate with the extent of their participation in the activity.
Method of Participation and Receipt of CME Certificate To obtain credit for this CME activity, you must:
CME Editor Disclosure: JACC: Cardiovascular Imaging CME Editor Ragavendra R. Baliga, MD, has reported that he has no relationships to disclose.
Author Disclosure: Dr. Narula has received research support in the form of an equipment grant to the institution from Philips Healthcare. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
1. Be an ACC member or JACC: Cardiovascular Imaging subscriber. 2. Carefully read the CME-designated article available online and in this
Medium of Participation: Print (article only); online (article and quiz).
issue of the journal. 3. Answer the post-test questions. At least 2 out of the 3 questions provided must be answered correctly to obtain CME credit. 4. Complete a brief evaluation.
CME Term of Approval Issue Date: September 2014 Expiration Date: August 31, 2015
From *The Zena and Michael A. Wiener Cardiovascular Institute/Marie-Josée and Henry R. Kravis Center for Cardiovascular Health, Mount Sinai Hospital, New York, New York; and the yCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain. Dr. Narula has received research support in the form of an equipment grant to the institution from Philips Healthcare. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose. Dr. Nathaniel Reichek has served as Guest Editor for this paper. Manuscript received April 1, 2014; revised manuscript received May 12, 2014, accepted May 13, 2014.
Pazos-López et al.
JACC: CARDIOVASCULAR IMAGING, VOL. 7, NO. 9, 2014 SEPTEMBER 2014:896–905
CMR for Cardiac Masses
Value of CMR for the Differential Diagnosis of Cardiac Masses ABSTRACT OBJECTIVES The goal of this study was to evaluate the diagnostic value of CMR features for the differential diagnosis of cardiac masses. BACKGROUND Differentiation of cardiac tumors and thrombi and differentiation of benign from malignant cardiac neoplasms is often challenging but important in clinical practice. Studies assessing the value of cardiac magnetic resonance (CMR) in this regard are scarce. METHODS We reviewed the CMR scans of patients with a definite cardiac thrombus or tumor. Mass characteristics on cine, T1-weighted turbo spin echo (T1w-TSE) and T2-weighted turbo spin echo (T2w-TSE), contrast first-pass perfusion (FPP), post-contrast inversion time (TI) scout, and late gadolinium enhancement (LGE) sequences were analyzed. RESULTS There were 84 thrombi, 17 benign tumors, and 25 malignant tumors in 116 patients. Morphologically, thrombi were smaller (median area 1.6 vs. 8.5 cm2; p < 0.0001), more homogeneous (99% vs. 46%; p < 0.0001), and less mobile (13% vs. 33%; p ¼ 0.007) than tumors. Hyperintensity compared with normal myocardium on T2w-TSE, FPP, and LGE were more common in tumors than in thrombi (85% vs. 42%, 70% vs. 4%, and 71% vs. 5%, respectively; all p < 0.0001). A pattern of hyperintensity/isointensity (compared with normal myocardium) with short TI and hypointensity with long TI was very frequent in thrombi (94%), rare in tumors (2%), and had the highest accuracy (95%) for the differentiation of both entities. Regarding the characterization of neoplastic masses, malignant tumors were larger (median area 11.9 vs. 6.3 cm2; p ¼ 0.006) and more frequently exhibited FPP (84% vs. 47%; p ¼ 0.03) and LGE (92% vs. 41%; p ¼ 0.001). The ability of CMR features to distinguish benign from malignant neoplasms was moderate, with LGE showing the highest accuracy (79%). CONCLUSIONS CMR features demonstrated excellent accuracy for the differentiation of cardiac thrombi from tumors and can be helpful for the distinction of benign versus malignant neoplasms. (J Am Coll Cardiol Img 2014;7:896–905) © 2014 by the American College of Cardiology Foundation.
A
lthough cardiac tumors are rare entities (esti-
dependent, offers poor tissue characterization, and
mated prevalence at autopsy of 0.02% to
has acoustic window restrictions in a subset of pa-
2.3%, and 0.15% in echocardiographic series)
tients. Transesophageal and 3-dimensional echocar-
(1), their morbidity and mortality rates are high (2).
diography may overcome some of these limitations
Surgical removal is the treatment option in most
(11,12). Computed tomography is also useful for the
cases, although satisfactory results occur only in
evaluation of tumors and thrombi (13), although at
benign types (3). Thrombi have a higher prevalence,
the expense of radiation exposure. As opposed to
ranging between 3% and 25% (4) and 2% and 50%
these modalities, cardiac magnetic resonance (CMR)
(5–7) in patients with atrial fibrillation and left ven-
has excellent contrast resolution that allows for su-
tricular systolic dysfunction, respectively, and justify
perior soft tissue characterization. The combined
anticoagulation to prevent embolic events (8,9).
evaluation of morphology, composition, and perfu-
Hence, proper differentiation among these entities
sion makes CMR a useful tool in the assessment of
remains imperative because both prognosis and ther-
cardiac masses (14–18). However, studies testing the
apeutic approach vary substantially.
accuracy of CMR in this regard are scarce and have
echocardiography
relatively small sample sizes (19–22). The aim of the
is the most common imaging technique used for
present study was to determine the ability of CMR
cardiac mass evaluation (10), but it is operator
features of cardiac masses to differentiate thrombus
Transthoracic
2-dimensional
897
898
Pazos-López et al.
JACC: CARDIOVASCULAR IMAGING, VOL. 7, NO. 9, 2014 SEPTEMBER 2014:896–905
CMR for Cardiac Masses
ABBREVIATIONS
from tumor and benign from malignant
(noninfiltrating lesion attached to the left aspect of
AND ACRONYMS
neoplasms in a larger population.
the fossa ovalis), septal lipomatosis (located in the interatrial septum with evident signal intensity
CMR = cardiac magnetic
METHODS
resonance
reduction on a fat saturation black-blood sequence), or cyst (well circumscribed, spherical or ovoid
FPP = first-pass perfusion LGE = late gadolinium enhancement
We retrospectively reviewed consecutive
shape, and high signal intensity on a T2-weighted
CMR examinations performed in patients
sequence); and 3) had a pathological diagnosis.
with a definite mass in the heart (including
T1w-TSE = T1-weighted turbo
aortic
and
pulmonary
roots)
Tumors were classified as malignant or benign on
spin echo
the
from
the basis of histology when available or otherwise on imaging characteristics different from the factors
T2w-TSE = T2-weighted turbo
January 2005 to March 2013 at Mount Sinai
spin echo
Hospital, New York. Definite thrombus was
tested in the study: infiltrating neoplasms were
TI = inversion time
defined as a noninfiltrating structure that
considered malignant, whereas noninfiltrating tu-
fulfilled any of the following classic criteria: 1) adja-
mors with typical features of myxoma, septal lip-
cent to an akinetic myocardial segment (often
omatosis, or cyst were classified as benign (Online
infarcted) or central venous catheter (without clinical
Figure 1). Clinical charts were reviewed for de-
signs or symptoms of infection); 2) located in the
mographic and medical data collection. In patients
atrial appendage in patients with documented atrial
undergoing surgery or biopsy, macroscopic and his-
fibrillation; 3) a significant size reduction occurred
tological findings were also recorded.
with anticoagulation therapy and confirmed on follow-up imaging; and 4) pathological confirmation.
CARDIAC
MAGNETIC
RESONANCE. CMR
studies
were performed on a 1.5-T (82%; Magnetom Sonata or Magnetom Avanto, Siemens Medical Solutions,
SEE PAGE 906
Erlangen, Germany) or a 3.0-T (18%; Ingenuity,
A mass was considered a definite tumor when it
Philips Healthcare, Best, the Netherlands) magnets
did not meet any of the aforementioned criteria and
by using dedicated phased-array surface coils as
fulfilled any of the following: 1) was infiltrative
receivers. Sequences were acquired during end-
(defined as ill-defined borders from normal myocar-
expiratory breath holds with electrocardiographic
dium and/or invasion of multiple cardiac or extra-
or pulse gating. Our typical protocol includes cine
cardiac structures); 2) had typical features of myxoma
and black-blood imaging before contrast, followed
T A B L E 1 Baseline Patient Characteristics
Male Age, yrs
Thrombus (n ¼ 77)
Tumor (n ¼ 39)
p Value
Benign Tumor (n ¼ 16)
Malignant Tumor (n ¼ 23)
52/77 (68)
17/39 (44)
0.013
4/16 (25)
13/23 (57)
58 15
60 15
0.85
60 11
61 18
0.9 0.13
p Value
0.051
77 17
79 16
0.61
83 15
75 16
10/75 (13)
3/39 (8)
0.37
2/16 (13)
1/23 (4)
0.58
82 28
94 37
0.39
79 57
97 35
0.54
Hypertension
44/77 (57)
18/38 (47)
0.32
9/15 (60)
9/23 (39)
0.21
Hyperlipidemia
38/77 (49)
13/38 (34)
0.12
8/15 (53)
5/23 (22)
0.045
Diabetes
23/77 (30)
9/38 (24)
0.49
5/15 (33)
4/23 (17)
0.44
Smoking history
23/77 (30)
12/38 (32)
0.85
3/15 (20)
9/23 (39)
0.29
Family history of CAD
14/77 (18)
5/38 (13)
Previous MI
45/76 (59)
1/39 (3)
Weight, kg Atrial fibrillation GFR, ml/min/1.73 m2
Previous stroke or embolic event Previous coronary revascularization History of malignancy
0.5