Hasiloglu Z I, Ure E, Comunoglu N, Tanriover N, Oz B, Gazioglu N, Mihmanli I
Department of Radiology, Istanbul University, Cerrahpasa Medical Faculty, Kocamustafapasa, Istanbul, Turkey.
Department of Radiology, Istanbul University, Cerrahpasa Medical Faculty, Kocamustafapasa, Istanbul, Turkey.
Clin Radiol. 2016 Sep;71(9):937.e5-937.e11. doi: 10.1016/j.crad.2016.04.022. Epub 2016 May 24.
To present three new cases of spindle cell oncocytoma (SCO) from a single centre and to identify new radiological clues in the diagnosis of SCO according to the information obtained from the cases presented.
Three adults with SCO confirmed at histopathology were retrospectively reviewed. The medical records, imaging findings, operative notes, and histopathology findings for each patient were recorded. Magnetic resonance imaging (MRI) findings were evaluated, including tumour localisation, tumour size, signal intensity, imaging features on T1-weighted and T2-weighted images, and contrast enhancement characteristics. The study protocol was approved by the institutional review board. Informed consent was obtained from each patient.
T1-weighted imaging (WI) and T2WI demonstrated millimetric hypointense foci and linear signal void areas in all lesions. Consistent with the hypervascular features of the tumour, intense contrast enhancement was observed during the early stages of dynamic contrast enhanced (DCE) MRI. Linear signal void areas showed contrast enhancement, but some of the hypointense millimetric foci remained without contrast enhancement.
Although the radiological findings and preoperative diagnosis of SCO have been reported to be non-specific and impossible, respectively, in the literature, the characteristics of MRI and different patterns of contrast enhancement can help in recognising this rare entity. This article represents a single institution case series of SCOs and also includes the first description of a correlation of the histopathological findings with radiological findings and new clues in the differential diagnosis of SCOs. We described these new radiological clues as "Hasiloglu's Signs".
介绍来自单一中心的三例新的梭形细胞嗜酸细胞瘤(SCO)病例,并根据所呈现病例获得的信息确定SCO诊断中的新影像学线索。
回顾性分析三例经组织病理学确诊为SCO的成年患者。记录每位患者的病历、影像学表现、手术记录和组织病理学结果。评估磁共振成像(MRI)表现,包括肿瘤定位、肿瘤大小、信号强度、T1加权和T2加权图像上的成像特征以及对比增强特征。该研究方案已获机构审查委员会批准。每位患者均签署了知情同意书。
T1加权成像(WI)和T2WI在所有病变中均显示出毫米级低信号灶和线性信号缺失区。与肿瘤的高血供特征一致,在动态对比增强(DCE)MRI早期观察到明显的对比增强。线性信号缺失区显示对比增强,但一些毫米级低信号灶仍无对比增强。
尽管文献报道SCO的影像学表现和术前诊断分别是非特异性的且不可能的,但MRI特征和不同的对比增强模式有助于识别这种罕见实体。本文展示了一个单一机构的SCO病例系列,还首次描述了组织病理学结果与影像学结果的相关性以及SCO鉴别诊断中的新线索。我们将这些新的影像学线索描述为“哈西洛格鲁征”。