Li Xue-Ming, Yang Hong, Reng Jing, Zhou Peng, Cheng Zhu-Zhong, Li Zhen, Xu Guo-Hui
Department of Radiology, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China Department of Pathology, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China Department of Urology, Sichuan Cancer Hospital and Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan China.
Medicine (Baltimore). 2017 Nov;96(45):e8551. doi: 10.1097/MD.0000000000008551.
Angiosarcoma is an extremely rare malignant tumor of endothelial origin. The majority of studies reporting angiosarcoma have been concerned with the clinical and pathological aspects, with limited reporting of their imaging findings. To our knowledge, angiosarcoma of the adrenal gland is very rare. Herein we firstly report a primary adrenal angiosarcoma depicted on magnetic resonance imaging (MRI).
A 59-year-old man was referred to our hospital for 1 year left-flank pain that exacerbated in recent 4 months.
A regular mass with clear boundary was revealed on MRI in the region of left adrenal gland. Its signal intensity was inhomogeneous. It mainly showed isointensity with patchy slight hyperintensity on T1-weighted images and marked hyperintensity with patchy hypointensity on T2-weighted images. On contrast-enhanced images, it demonstrated significantly heterogeneous enhancement, and the peripheral solid component showed delayed enhancement. Bulky blood vessels and hemorrhage were identified in the tumor.
The mass was surgically excised under a left laparoscopic adrenalectomy.
Left adrenal angiosarcoma was confirmed by pathological and immunohistochemical examinations. No evidence of recurrence was found 6 months after operation.
In conclusion, primary adrenal angiosarcoma has some MRI features corresponding to its pathological nature. It should be included in the differential diagnosis when a mass was detected in the adrenal gland.
血管肉瘤是一种极其罕见的起源于内皮细胞的恶性肿瘤。大多数报道血管肉瘤的研究都关注其临床和病理方面,对其影像学表现的报道有限。据我们所知,肾上腺血管肉瘤非常罕见。在此我们首次报告一例经磁共振成像(MRI)显示的原发性肾上腺血管肉瘤。
一名59岁男性因左侧腰痛1年,近4个月加重而转诊至我院。
MRI显示左侧肾上腺区域有一个边界清晰的规则肿块。其信号强度不均匀。在T1加权图像上主要表现为等信号伴斑片状轻度高信号,在T2加权图像上表现为明显高信号伴斑片状低信号。在增强图像上,它显示出明显的不均匀强化,外周实性成分呈延迟强化。肿瘤内可见粗大血管和出血。
通过左侧腹腔镜肾上腺切除术将肿块手术切除。
病理及免疫组化检查证实为左侧肾上腺血管肉瘤。术后6个月未发现复发迹象。
总之,原发性肾上腺血管肉瘤具有一些与其病理性质相对应的MRI特征。当肾上腺发现肿块时,应将其纳入鉴别诊断。