Int J Cardiol. 2010 Apr 15;140(2):e23-6. doi: 10.1016/j.ijcard.2008.11.072. Epub 2009 Jan 7.
A 46-year-old man was first diagnosed as Buerger's disease according to his clinical and radiological features because he had no evidence of parasitic, allergic and connective tissue disease. Soft subcutaneous nodules suspected of lymphadenopathy on the bilateral inguinal regions were recognized after admission. Positron emission tomography scan showed the increased uptake of (18)F-fluoro-2-deoxyglucose in the bilateral inguinal regions. We finally diagnosed him as Kimura's disease based on pathologic findings and laboratory data, and started steroid therapy. The uptake of (18)F-fluoro-2-deoxyglucose disappeared and his leg pain was improved after the treatment. This is the first case report presenting a patient of Kimura's disease with Buerger's disease-like vasculitis who was demonstrated by positron emission tomography.
一位 46 岁男性,因临床和影像学特征首先被诊断为伯格病,因为他没有寄生虫、过敏和结缔组织疾病的证据。入院后,在双侧腹股沟区发现疑似淋巴结病的软皮下结节。正电子发射断层扫描显示双侧腹股沟区(18)F-氟-2-脱氧葡萄糖摄取增加。根据病理发现和实验室数据,我们最终诊断为他为 Kimura 病,并开始类固醇治疗。治疗后,(18)F-氟-2-脱氧葡萄糖摄取消失,腿部疼痛改善。这是首例报告表现为伯格病样血管炎的 Kimura 病患者,正电子发射断层扫描显示。