Primary nasopharyngeal non-Hodgkin ’ s lymphoma: imaging patterns on MR imaging

Abstract Objectives To summarize the distinct imaging features of different subtypes of primary nasopharyngeal non-Hodgkin's lymphomas (NHLs). Materials and methods Clinical data and magnetic resonance imaging findings of 71 patients with histologically proven primary nasopharyngeal NHLs were r...

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Veröffentlicht in:Clinical imaging 2013, Vol.37 (3), p.458-464
Hauptverfasser: Xie, Chuan-miao, Liu, Xue-wen, Mo, Yun-xian, Li, Hui, Geng, Zhi-jun, Zheng, Lie, Lv, Yan-chun, Ban, Xiao-hua, Zhang, Rong
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Sprache:eng
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Zusammenfassung:Abstract Objectives To summarize the distinct imaging features of different subtypes of primary nasopharyngeal non-Hodgkin's lymphomas (NHLs). Materials and methods Clinical data and magnetic resonance imaging findings of 71 patients with histologically proven primary nasopharyngeal NHLs were retrospectively reviewed. The tumor distribution, signal intensity, lesion texture, contrast enhancement properties, extra-chamber involvement, regional structure invasion, and cervical lymphadenopathy were evaluated and compared between different subtypes of NHLs. Results Of the patients, 70.4% had B-cell lymphomas; 64.8% had symmetrical and diffuse involvement of nasopharynx walls; and 19.7% had superficial ulcerations. Extra-chamber involvement and regional structure invasion occurred in most patients. The frequency of neck node involvement was up to 83.10%; 62.7% of them were bilateral involvement. Patients with T-cell or nature killer/T-cell NHLs had a higher incidence of superficial ulcerations, nasal cavity, and paranasal sinus invasion than B-cell NHLs ( P < .05). Patients with B-cell NHLs had a higher incidence of cervical lymphadenopathy specifically in Level VA and parotid region than T-cell or nature killer/T-cell (NK/T-cell) NHLs ( P < .05). Conclusion Primary nasopharyngeal NHLs had some characteristic imaging features and different subtypes of nasopharyngeal NHLs had some distinct imaging features.
ISSN:0899-7071
DOI:10.1016/j.clinimag.2012.07.009