MR imaging of thymic epithelial tumors: correlation with World Health Organization classification

The aim of this study was to determine magnetic resonance imaging (MRI) features of various subtypes of thymic epithelial tumors based on the World Health Organization classification. The study included 64 patients with histologically proven thymic epithelial tumors. Two observers evaluated the MRI...

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Veröffentlicht in:Japanese journal of radiology 2006-04, Vol.24 (3), p.171-181
Hauptverfasser: Inoue, Atsuo, Tomiyama, Noriyuki, Fujimoto, Kiminori, Sadohara, Junko, Nakamichi, Itsuko, Tomita, Yasuhiko, Aozasa, Katsuyuki, Tsubamoto, Mitsuko, Murai, Sachiko, Natsag, Javzandulam, Sumikawa, Hiromitsu, Mihara, Naoki, Honda, Osamu, Hamada, Seiki, Johkoh, Takeshi, Nakamura, Hironobu
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Sprache:eng
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Zusammenfassung:The aim of this study was to determine magnetic resonance imaging (MRI) features of various subtypes of thymic epithelial tumors based on the World Health Organization classification. The study included 64 patients with histologically proven thymic epithelial tumors. Two observers evaluated the MRI findings in terms of tumor size, contour, lobulation, shape, homogeneity, the presence of intratumor high- and low-signal foci, enhancement degree and pattern, the presence of capsule and septum, and associated mediastinal lymphadenopathy and pleural effusion. Type A tumors were more likely to have a smooth contour, round shape, distinct capsule, and smaller size compared to any other type of thymic epithelial tumor. Thymic carcinomas demonstrated a higher prevalence of low-signal foci within the mass on T2-weighted images and mediastinal lymphadenopathy than any other types. The frequency of heterogeneous intensity on T2-weighted images increased from type A tumors to thymic carcinomas. The presence of a smooth contour, round shape, and capsule is highly suggestive of a type A tumor. Foci of low signal intensity in the mass on T2-weighted images and mediastinal lymphadenopathy are highly suggestive of thymic carcinomas.
ISSN:0288-2043
1867-1071
1862-5274
1867-108X
DOI:10.1007/s11604-005-1530-4