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Published online before print April 26, 2007, 10.1148/radiol.2433060797
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(Radiology 2007;243:869-876.)
© RSNA, 2007

Thoracic Imaging

Thymic Hyperplasia and Thymus Gland Tumors: Differentiation with Chemical Shift MR Imaging1

Tsutomu Inaoka, MD, Koji Takahashi, MD, PhD, Masayuki Mineta, MD, PhD, Tomonori Yamada, MD, Noriyuki Shuke, MD, PhD, Atsutaka Okizaki, MD, Kenichi Nagasawa, MD, Hiroyuki Sugimori, RT, and Tamio Aburano, MD, PhD

1 From the Department of Radiology, Asahikawa Medical College, 2-1-1-1 Midorigaoka-Higashi, Asahikawa 078-8510, Japan. From the 2005 RSNA Annual Meeting. Received May 6, 2006; revision requested June 27; revision received July 29; final version accepted September 18. Address correspondence to T.I. (e-mail: tinaoka{at}asahikawa-med.ac.jp).

Purpose: To prospectively evaluate chemical shift magnetic resonance (MR) imaging for differentiating thymic hyperplasia from tumors of the thymus gland.

Materials and Methods: The institutional review board approved this study; informed consent was obtained and patient confidentiality was protected. The authors assessed 41 patients (17 male, 24 female; age range, 16–78 years) in whom thymic lesions were seen at chest computed tomography. Patients were assigned to a hyperplasia group (n = 23) (18 patients with hyperplastic thymus associated with Graves disease and five with rebound thymic hyperplasia) and a tumor group (n = 18) (seven patients with thymomas, four with invasive thymomas, five with thymic cancers, and two with malignant lymphomas). T2-weighted fast spin-echo and T1-weighted in-phase and opposed-phase MR images were obtained in all patients and visually assessed. A chemical shift ratio (CSR), determined by comparing the signal intensity of the thymus gland with that of the paraspinal muscle, was calculated for quantitative analysis. Mean CSRs for the patient groups and subgroups were analyzed by using Welch t and Newman-Keuls tests. P < .05 indicated a significant difference.

Results: The thymus gland had homogeneous signal intensity in all 23 patients in the hyperplasia group and in 12 of the 18 patients in the tumor group. The mean CSR (± standard deviation) was 0.614 ± 0.130 in the hyperplasia group and 1.026 ± 0.039 in the tumor group. Mean CSRs in the patients with a hyperplastic thymus and Graves disease, rebound thymic hyperplasia, thymoma, invasive thymoma, thymic cancer, and malignant lymphoma were 0.594 ± 0.120, 0.688 ± 0.154, 1.033 ± 0.043, 1.036 ± 0.040, 1.020 ± 0.044, and 0.997 ± 0.010, respectively. The difference in CSR between the hyperplasia and tumor groups was significant (P < .001). Mean CSRs in the hyperplasia subgroups were lower than those in the tumor subgroups (P < .001). All hyperplasia group patients had an apparent decrease in thymus gland signal intensity at chemical shift MR imaging; no tumor group patients had a decrease in thymus gland signal intensity.

Conclusion: Chemical shift MR imaging can be used to differentiate thymic hyperplasia from thymic tumors.

© RSNA, 2007