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“满堂亮”增殖性肾小球肾炎:亚急性感染性心内膜炎的一种未报道表现。

"Full house" proliferative glomerulonephritis: an unreported presentation of subacute infective endocarditis.

作者信息

Lee L-C, Lam K-K, Lee C-T, Chen J-B, Tsai T-H, Huang S-C

机构信息

Department of Internal Medicine, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Chang Gung University College of Medicine, Kaohsiung - Taiwan.

出版信息

J Nephrol. 2007 Nov-Dec;20(6):745-9.

Abstract

A severely ill 65-year-old man presented with symptoms of shortness of breath, edema and vasculitidic purpura over his lower extremities. He had severe mitral regurgitation which had not been surgically treated. Hematologic examination demonstrated leukocytosis with profound anemia. Other blood tests revealed impaired renal function, hypoalbuminemia, hypocomplementemia and mixed-type cryoglobulinemia. Urinalysis showed proteinuria, hematuria and pyuria, typical of a nephritic sediment. Renal biopsy indicated diffuse proliferative glomerulonephritis and a "full house" deposition in immunofluorescence study (positive for C3, C4, C1q, IgG, IgA and IgM), resembling the pathologic findings in class IV lupus nephritis. Although subacute bacterial endocarditis was initially suspected owing to a history of a predisposing valvular heart disease, probable vegetation shown by cardiac sonography and a clinical picture suggestive of a chronic infection, it was thought unlikely due to the entire afebrile course and initial sterile blood cultures. However, the blood cultures repeated 2 weeks after admission grew 3 sets of viridans streptococci. Following a course of penicillin and gentamicin treatment, his renal function, anemia and abnormal urine sediments improved gradually. Diffuse proliferative glomerulonephritis is well known to occur in infective endocarditis. However, the "full house" immunostaining in immunofluorescence study has never been reported. This case adds a new entity to the differential diagnosis of "full house" immune complex-related glomerulonephritis and exemplifies the need to maintain a high index of suspicion for underlying infectious disorders when facing glomerulonephritic or vasculitic syndrome.

摘要

一名65岁重症男性,出现呼吸急促、下肢水肿及血管炎性紫癜症状。他患有严重二尖瓣反流,未接受手术治疗。血液学检查显示白细胞增多伴严重贫血。其他血液检查显示肾功能受损、低白蛋白血症、补体减少及混合型冷球蛋白血症。尿液分析显示蛋白尿、血尿及脓尿,为典型的肾炎性沉渣。肾活检提示弥漫性增生性肾小球肾炎,免疫荧光检查呈“满堂亮”沉积(C3、C4、C1q、IgG、IgA及IgM均为阳性),类似IV型狼疮性肾炎的病理表现。尽管最初因有易患瓣膜性心脏病史、心脏超声显示可能存在赘生物及提示慢性感染的临床表现而怀疑亚急性细菌性心内膜炎,但鉴于整个病程无发热且初始血培养无菌,故认为可能性不大。然而,入院2周后重复进行的血培养培养出3组草绿色链球菌。经过青霉素和庆大霉素治疗后,他的肾功能、贫血及异常尿沉渣逐渐改善。众所周知,弥漫性增生性肾小球肾炎可发生于感染性心内膜炎。然而,免疫荧光检查中的“满堂亮”免疫染色此前从未有过报道。该病例为“满堂亮”免疫复合物相关肾小球肾炎的鉴别诊断增添了新的病种,并例证了面对肾小球肾炎或血管炎综合征时,对潜在感染性疾病保持高度怀疑的必要性。

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