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Original Report |
1 Department of Radiology, GRB-290, Massachusetts General Hospital, 55 Fruit
St., Boston, MA 02114.
2 Present address: Department of Radiology, Singapore General Hospital,
Singapore.
Received February 17, 2004;
accepted after revision May 14, 2004.
C-M Fan and S. L. Aquino have each made substantial contributions to the
design and analysis of this work and the writing of the article. Each of them
is equally responsible for the integrity of all data in the article and for
the correctness of the analysis and conclusions supported by those data.
Abstract
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CONCLUSION. Increased FDG uptake occurs in LHIS, a benign fatty infiltration of the interatrial septum. Increased uptake in the right heart on FDG PET warrants correlation with additional imaging to assess for LHIS and avoid false interpretation of malignancy.
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In all patients, CT scans of the thorax were acquired within 30 days of the FDG PET scans. Six patients had serial CT scans from 1- to 5-year intervals that verified the stability of the LHIS. Two additional patients without prior CT scans underwent cardiac MRI to evaluate the abnormal FDG PET uptake in the right heart.
CT Protocol
CT was performed using a HiSpeed or Light-Speed scanner (GE Healthcare).
Scans were obtained at a 5-mm slice interval during a single breath-hold with
IV contrast material (100 mL of ioxilan, 300 mg I/mL) administered at an
injection rate of 2 mL/sec. The thoracic CT scans were reviewed by two
radiologists. The dimensions of the interatrial septum were measured anterior
and posterior to the fossa ovalis. The Hounsfield unit measurements of the
atrial septal tissue also were obtained to confirm the presence of fat
density.
MRI Protocol
Cardiac MR scans were obtained on a Sigma CVI 1.5-T clinical system (GE
Healthcare). The patients were scanned in the supine position with a cardiac
phased-array coil. ECG-gated and respiratorygated high-resolution axial
conventional spin-echo images were acquired with 7-mm slice thickness, 1-mm
gap, and matrix size of 256 (frequency-encoding steps) x 224
(phase-encoding steps). The TR was equal to one cardiac cycle length, and the
TE was set at 8 msec; the number of excitations was 4. The sequence was
repeated at identical spatial coordinates and time points in the cardiac cycle
using identical scanning parameters except that chemical fat saturation was
used.
FDG PET Protocol
FDG PET studies were performed using an ECAT-HR+ camera (Siemens/CTI). The
patients fasted for at least 6 hr before scanning, and blood glucose levels
were measured before injection of FDG. From 15 to 20 mCi (555740 GBq)
of FDG was administered IV as a bolus, and static emission images were
obtained 60 min later in multiple bed positions, each 10 min in duration.
Transmission images, measured with rotating rod sources loaded with 68Ge, were
obtained in each bed position for attenuation correction. Image reconstruction
was performed with ordered subset expectation maximization algorithms. The
dose, time of injection, and the patient's body weight were used to calculate
the peak standardized uptake value (SUV). The SUV was calculated at the region
of increased uptake at the interatrial septum, the middle mediastinum (above
the left ventricle), and the liver.
FDG PET scans and CT scans were reviewed with and without fusion overlay using the computer registration software and viewing station of REVEAL-MVS (Mirada Solutions). The degree of FDG activity was graded visually as no discernible uptake or as uptake less than, equal to, or greater than background mediastinal activity.
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FDG PET showed focal increased FDG uptake in nine patients (82%), corresponding to the regions of LHIS on CT (Figs. 1A, 1B, 1C, 1D, 1E, 2A, 2B, 2C, 2D, 2E, and 2F). In these nine patients, the SUV of the interatrial septum was 1.66.1 times greater than the SUV of the mediastinum blood pool. The mean SUV of the atrial septa was 5.6 (range, 1.813.4) compared with the mean mediastinal blood pool SUV of 1.8 (range, 1.32.3) and mean liver SUV of 2.1 (range, 1.62.5). In two patients with LHIS on CT, there was no evidence of increased FDG uptake in the interatrial septum on PET. Their mean septal SUV was 1.0, whereas it was 2.0 and 2.2 in the mediastinum blood pool and liver, respectively. The FDG PET findings are summarized in Table 2.
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MR images were obtained in two patients. In both patients the interatrial septum displayed increased signal on T1-weighted images with signal dropout on T1-weighted images acquired with fat-saturation, confirming fat density (Figs. 1A, 1B, 1C, 1D, and 1E).
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The histologic features of LHIS were examined in detail by Page [11], who analyzed the septal fat deposition pattern in 50 unselected hearts compared with 10 selected cases of extreme fatty enlargement of the interatrial septum. Page found that septal fat deposits increase with patient age, are contiguous with epicardial fat deposits, and correlate with increased epicardial fat in obese individuals. With increased septal fat infiltration, there is progressive disruption and disorganization of the myocardial fibers with development of fibrosis. These changes are implicated in the pathogenesis of impaired contractility and electrical conduction, which may underlie the infrequent association of LHIS with supraventricular arrhythmias and sudden death.
In LHIS, the masslike fat deposits are not encapsulated but may appear constrained at the margins by normal structures including the pericardium, fossa ovalis, atrial walls, and atrioventricular groove. LHIS has a characteristic bilobed appearance on cross-sectional imaging at the level of the fossa ovalis due to fat accumulation in the anterior and posterior septum, with sparing of the fossa ovalis itself. The diagnosis is confirmed by detection of nonenhancing fat density on CT or fat signal intensity within the characteristically shaped lesion on MRI [1] (Figs. 1A, 1B, 1C, 1D, and 1E). In our series, we noted marked preferential FDG uptake within the atrial septa in nine of 11 patients with CT or MRI confirmation (or both) of LHIS. Preferential uptake of FDG by brown fat, especially in the nonfasting state, has been reported in the rat model [12]. Not all of our patients with LHIS had increased uptake of FDG on PET, and we postulate that variable presence of brown fat in LHIS may be responsible for this finding.
It is important to recognize that increased FDG uptake in benign processes potentially can mimic malignancy either in adjacent lymph nodes or in the myocardium. False interpretation of increased FDG uptake as neoplasm in LHIS would stage a patient with malignancy inappropriately as having a metastasis and potentially result in suboptimal therapy. Fusion PET/CT helps clarify the region of localized FDG uptake and confirm that it lies in the region of LHIS rather than the adjacent right hilum, mediastinum, or pleura.
Our study is retrospective and therefore we cannot determine the prevalence of LHIS in our population. Another major limitation of this study is the absence of histologic confirmation of LHIS in our patients because none of them underwent an intracardiac biopsy. However, we were able to confirm the presence of fat in the LHIS on MRI in two patients and document stability of the LHIS on serial CT (Figs. 2A, 2B, 2C, 2D, 2E, and 2F) in six.
In conclusion, LHIS is a relatively frequent and usually clinically innocuous abnormality of the heart. We have found that LHIS can show increased FDG uptake on PET. This finding may be related to the presence of brown fat, which can be present in LHIS and has been reported to show increased FDG uptake in the rat model. We recommend that when increased uptake is seen within the right heart on FDG PET, correlation with CT and possibly MRI be performed to assess for the presence of LHIS and to avoid the false-positive diagnosis of malignancy.
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