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作 者:何龙芝 葛玉成 赵振强 刘宇坤 齐思宇 宁晨[1] 王文营[1] He Longzhi;Ge Yucheng;Zhao Zhenqiang;Liu Yukun;Qi Siyu;Ning Chen;Wang Wenying(Department of Urology,Beijing Friendship Hospital,Capital Medical University,Beijing 100050,China)
机构地区:[1]首都医科大学附属北京友谊医院泌尿外科,北京100050
出 处:《中华泌尿外科杂志》2024年第5期395-396,共2页Chinese Journal of Urology
摘 要:IgC4相关性疾病(IgC4-RD)累及输尿管表现为输尿管肿物罕见,本文报道1例女性患者,因体检发现左肾盂输尿管连接处肿物1周就诊。超声及MRI检查示左肾盂输尿管连接处有一长径约3cm的肿物,伴左肾积水,血清IgG4浓度升高。行B超引导下肿物穿刺活检,病理提示淋巴浆细胞浸润,IgG4/IgG>0.5,考虑为IgG4-RD。患者接受糖皮质激素治疗1个月后复查CT见肿物明显缩小,IgG4浓度下降至正常。IgG4-related disease(IgG4-RD)involving the ureter manifested as a ureteral tumor is rare.This paper reports a case of a female patient who was found with a mass at the left ureteropelvic junction for one week during physical examination.Urinary ultrasound and MRI showed a 3 cm mass at the left ureteropelvic junction with hydronephrosis,and the serum level of IgG4 was elevated.B-ultrasonic guided biopsy of the mass was performed.Histopathological findings showed lymphoplasmic infiltration and the ratio of IgG4/IgG positive cells>0.5.We finally diagnosed IgG4-RD and started using glucocorticoid for her treatment.One month later,CT-scan revealed that the tumor became smaller and the serum IgG4 decreased to the normal range.
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