Department of Otorhinolaryngology, Martin-Luther-University Halle-Wittenberg, Ernst-Grube-Str. 40, 06097 Halle, Germany.
Eur J Radiol. 2013 Feb;82(2):302-8. doi: 10.1016/j.ejrad.2012.03.036. Epub 2012 Oct 23.
Primary extranodal lymphomas of the orbit and sinonasal region are rare and occur almost only as Non-Hodgkin lymphoma (NHL). The purpose of this study was to determine the frequency of different subtypes of NHL in these regions and to describe their radiological features.
Between January 2005 and January 2010, 567 patients with malignant immunoproliferative diseases (MID) were treated at our institution. Primary sinonasal and orbital manifestation was diagnosed in 36 cases. There were 13 women and 23 men with a median age of 67 years. CT and MRI were performed in 14 and 24 patients, respectively. Imaging was re-interpretated and histological subtypes were listed.
Among all MID primary sinonasal and orbital NHL occurred with a frequency of 6%. Diffuse large cell lymphoma was identified in 11 cases (30%), marginal cell lymphoma in 6 (16%), and extranodal plasmacytoma in 5 (14%). Other subtypes were rare. On CT, lesions of soft tissue attenuation with homogeneous moderate contrast enhancement were seen in all cases. On T2-weighted fat saturated images 52% of the lesions were slightly hyperintense in comparison to unaffected musculature, 41% were isointense, and 7% slightly hypointense. On T1-weighted sequences most lesions (81%) were homogeneously isointense. After contrast administration marked enhancement was seen in 41%, moderate in 52%, and slight enhancement in 7%.
The identified radiological features should be included in the differential analysis of lesions in the orbital and sinonasal regions, but they are not specific enough. For exact therapeutic planning histopathological diagnosis of the subtype is required.
眼眶和鼻腔鼻窦原发性结外淋巴瘤十分罕见,几乎均为非霍奇金淋巴瘤(NHL)。本研究旨在确定这些部位 NHL 的不同亚型的频率,并描述其影像学特征。
2005 年 1 月至 2010 年 1 月期间,我们机构治疗了 567 例恶性免疫增殖性疾病(MID)患者。诊断为原发性鼻腔鼻窦和眼眶表现的有 36 例。患者为 13 名女性和 23 名男性,中位年龄为 67 岁。分别对 14 例和 24 例患者进行了 CT 和 MRI 检查。重新解读了影像学资料,并列出了组织学亚型。
在所有 MID 中,原发性鼻腔鼻窦和眼眶 NHL 的发生率为 6%。弥漫性大 B 细胞淋巴瘤 11 例(30%),边缘区淋巴瘤 6 例(16%),结外浆细胞瘤 5 例(14%)。其他亚型罕见。CT 上,所有病例均可见软组织衰减病变,呈均匀中等程度对比增强。T2 加权脂肪饱和图像上,52%的病变与未受影响的肌肉相比轻度高信号,41%等信号,7%轻度低信号。T1 加权序列上,大多数病变(81%)均匀等信号。增强后,41%明显强化,52%中度强化,7%轻度强化。
所识别的影像学特征应纳入眼眶和鼻腔鼻窦病变的鉴别分析,但它们不够特异。为了进行精确的治疗计划,需要进行组织学亚型的病理诊断。