Department of Urology, People's Hospital of Hainan Province, Haikou, China.
The University of North Carolina at Chapel Hill, USA.
J Xray Sci Technol. 2018;26(1):141-146. doi: 10.3233/XST-17345.
Rosai-Dorfman disease (RDD) is a rare histiocytic disorder of unclear etiology, which commonly presented with the enlargement of lymph nodes of the neck and the head. Here, we report an unusual case of 77-year-old male patient presenting with left kidney lesion with several small enlarged lymph nodes around the abdominal aorta. The diagnosis of left kidney cancer was suspected and the patient underwent left laparoscopic exploration and lymph node biopsy. Only saponification of the renal surrounding fat and enlargement of the left renal pedicle and 5 abdominal aortic lymph nodes were found; no kidney cancer was found. Surrenalectomy and lymphadenectomy dissection were then performed and the left kidney was retained. Intraoperative frozen and postoperative pathology indicates Rosai-Dorfman disease. RDD with kidney involvement is uncommon, and its x-ray imaging appearances are atypical, and often resemble kidney cancer leading to kidney loss. A systematic literature review was also performed to investigate the x-ray imaging and treatment features of this disease.
罗-道二氏病(RDD)是一种病因不明的罕见组织细胞增生症,常表现为颈部和头部淋巴结肿大。我们在此报告一例 77 岁男性患者,其左肾病变伴腹主动脉周围数个小淋巴结肿大。诊断为左肾癌,患者行左腹腔镜探查及淋巴结活检术。仅发现肾周围脂肪皂化和左肾蒂及 5 个腹主动脉淋巴结肿大,未见肾癌。随后行肾上腺切除术和淋巴结清扫术,保留左肾。术中冰冻和术后病理提示罗-道二氏病。肾脏受累的 RDD 并不常见,其 X 线影像学表现不典型,常类似于肾癌导致肾脏丢失。还进行了系统的文献复习,以研究该病的 X 线影像学和治疗特征。