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MR imaging of cheek lesions of Kimura’s disease: Focusing on the signal abnormalities and the relationship with superficial musculoaponeurotic systems

机译:木村病脸颊病变的MR成像:着眼于信号异常以及与浅表肌腱膜系统的关系

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Background and Purpose: Kimura’s Disease (KD) is a rare benign chronic eosinophlic inflammatory disorder, characterized by angiolymphoid proliferation with peripheral eosinophilia and elevated serum immunoglobulin E. Most lesions occur in the head and neck regions. To the best of our knowledge, the relationship between subcutaneous cheek lesion of KD and the surrounding structures including superficial musculoaponeurotic systems (SMAS) has never been reported. The purpose of this study was to describe MR imaging findings of cheek subcutaneous lesion of KD and adjacent SMAS. Materials and Methods: Seven cheek subcutaneous lesions of 5 patients histopathologically proved KD were evaluated. We retrospectively evaluated the MR imaging findings of subcutaneous lesions for signal intensity in each imaging sequence, the border of the lesions, and appearance of SMAS. Results: All cheek lesions were displacing normal fat tissue. These lesions showed ill-defined border (7/7), slightly high signal intensity on T1-weighted images (7/7), and intermediate (1/7) or high signal intensity (6/7) on T2-weighted images. Cheek lesions were enhanced by intravenous injection of gadolinium to signal intensity close to that of fat tissue (3/4), and in one case, the avid enhancement of the mass was seen (1/4). All lesions attached to the outer surface of SMAS, however, only one out of 7 lesions distributed below the SMAS without tearing of the layers. SMAS below the lesion showed high signal intensity on T2-weighted images in two lesions (2/7). Conclusion: KD should be included in the differential diagnosis when a cheek mass presents with non-specific signal intensities and irregular border, which attaches to but does not interrupt SMAS on MR imaging.
机译:背景与目的:木村病(Kimura's Disease,KD)是一种罕见的良性慢性嗜酸性粒细胞性炎性疾病,其特征是血管淋巴样增生,伴有外周嗜酸性粒细胞增多和血清免疫球蛋白E升高。大多数病变发生在头部和颈部。据我们所知,KD的皮下颊部病变与包括浅表肌腱膜系统(SMAS)在内的周围结构之间的关系从未被报道过。这项研究的目的是描述KD和邻近的SMAS的颊部皮下病变的MR影像学表现。材料和方法:对5例经组织病理学证实为KD的患者的7个颊颊皮下病变进行了评估。我们回顾性评估了皮下病变的MR成像发现,以了解每个成像序列中的信号强度,病变的边界以及SMAS的外观。结果:所有脸颊病变均移位正常脂肪组织。这些病变显示边界不清晰(7/7),在T1加权图像上显示较高的信号强度(7/7),在T2加权图像上显示中间(1/7)或高信号强度(6/7)。静脉注射g可增强脸颊病变,使其信号强度接近脂肪组织(3/4),在一种情况下,可见肿块明显增强(1/4)。所有的病灶都附着在SMAS的外表面,但是,只有7个病灶中的1个分布在SMAS下方,而没有撕裂各层。病变下方的SMAS在两个病变(2/7)的T2加权图像上显示出高信号强度。结论:当脸颊肿块表现出非特异性信号强度和不规则边界时,KD应包括在鉴别诊断中,其附着在MR成像上但不会中断SMAS。

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