Sehgal Rahul, Sajjad Syed M, Thapa Jiwan K
Department of Rheumatology, Mayo Clinic, Eau Claire, Wisconsin, USA
Department of Pathology, Marshfield Clinic Health System, Marshfield, Wisconsin, USA.
Clin Med Res. 2017 Dec;15(3-4):100-105. doi: 10.3121/cmr.2017.1371. Epub 2017 Dec 1.
Renal involvement in primary Sjogren's syndrome (pSS) varies in severity and prevalence. Although previously felt to be uncommon, kidneys can be involved in 25% to 30% of pSS patients. Fibrillary glomerulonephritis (FGN) is a rare primary glomerular disease that can occur in association with another autoimmune condition or malignancy. The diagnosis relies on renal biopsy findings of haphazardly arranged fibrils in all glomerular compartments and distinction from other forms of fibrillary glomerulopathies such as renal amyloidosis and immunotactoid glomerulopathy. FGN responds poorly to immunosuppressive therapy and has a poor prognosis. Here, we describe a case of FGN in a patient with asymptomatic pSS. We describe the diagnostic work-up, clinical course, treatment utilized, and 1-year follow-up. There is one other case in the literature of FGN in a patient with pSS. The rarity of this association and distinction of FGN from other forms of renal involvement in pSS is important as it impacts therapy and prognosis. The case highlights electron microscopy findings in FGN and poor prognosis.
原发性干燥综合征(pSS)中的肾脏受累在严重程度和患病率方面存在差异。尽管此前认为并不常见,但肾脏可在25%至30%的pSS患者中受累。纤维性肾小球肾炎(FGN)是一种罕见的原发性肾小球疾病,可与另一种自身免疫性疾病或恶性肿瘤相关联。诊断依赖于肾活检发现所有肾小球区域内有杂乱排列的纤维,并与其他形式的纤维性肾小球病如肾淀粉样变性和免疫触须样肾小球病相鉴别。FGN对免疫抑制治疗反应不佳,预后较差。在此,我们描述一例无症状pSS患者发生FGN的病例。我们描述了诊断检查、临床病程、所采用的治疗方法以及1年随访情况。文献中还有另一例pSS患者发生FGN的病例。这种关联的罕见性以及FGN与pSS中其他形式肾脏受累的区别很重要,因为它会影响治疗和预后。该病例突出了FGN的电子显微镜检查结果及不良预后。