Department of Nephrology, Japanese Red Cross Society Kyoto Daiichi Hospital, 15-749 Honmachi Higashiyamaku Kyoto-Shi, Kyoto, 606-0981, Japan.
CEN Case Rep. 2023 May;12(2):200-204. doi: 10.1007/s13730-022-00752-9. Epub 2022 Nov 11.
This is a case report of a 69-year-old Japanese man who has been undergoing treatment for primary Sjögren's syndrome (pSS) since he was 62 years. A renal biopsy, which revealed diffuse and severe mononuclear cell infiltration in the tubulointerstitium, was performed because of progressive renal dysfunction. Immunostaining demonstrated most of the infiltrating cells to be IgA, kappa, CD38, and CD138 positive. Immunofixation blood test revealed IgA kappa-type M protein; however, bone marrow abnormalities or lymph node enlargements on examination or imaging, respectively, were not observed. Tubulointerstitial nephritis caused by monotypic plasmacytic infiltration in pSS, accompanied with a monoclonal gammopathy of undetermined significance (MGUS), was diagnosed. A treatment of prednisolone 40 mg/day was initiated, promptly improving the patient's serum creatinine levels from 3.0 to 1.5 mg/dl. The infiltrating cells in pSS-associated tubulointerstitial nephritis are generally polytypic plasmacytes and lymphocytes, but in the present case, monotypic plasmacytes were predominant. This case is remarkable and rare and can be considered a complication of pSS or MGUS. Since it may become a new disease entity, it is important to accumulate similar cases.
这是一例 69 岁日本男性病例报告,他自 62 岁起一直接受原发性干燥综合征(pSS)的治疗。由于进行性肾功能障碍,进行了肾活检,结果显示弥漫性和严重的单核细胞浸润在肾小管间质中。免疫组化染色显示大多数浸润细胞为 IgA、kappa、CD38 和 CD138 阳性。免疫固定血检显示 IgA kappa 型 M 蛋白;然而,分别在检查或影像学上均未观察到骨髓异常或淋巴结肿大。诊断为 pSS 引起的单克隆浆细胞浸润伴意义未明的单克隆丙种球蛋白血症(MGUS)的肾小管间质性肾炎。开始给予泼尼松龙 40mg/天治疗,迅速将患者的血清肌酐水平从 3.0 提高到 1.5mg/dl。pSS 相关肾小管间质性肾炎中的浸润细胞通常为多克隆浆细胞和淋巴细胞,但在本病例中,单克隆浆细胞占优势。该病例罕见且显著,可被视为 pSS 或 MGUS 的并发症。由于它可能成为一种新的疾病实体,因此积累类似病例很重要。