Collapsing FSGS with Concurrent Class 2 and 3 Lupus Nephritis: A Case Report and Review of the Literature

被引:1
|
作者
Vanood, Aimen [1 ]
Owen, Ryan [1 ,2 ]
Maraskine, Marina [1 ,2 ]
Schreiber, Ariyon [1 ]
Pokharel, Rajesh [1 ,2 ]
Cohen, Lisa [1 ,3 ]
机构
[1] Oakland Univ, William Beaumont Sch Med, Rochester, MI 48063 USA
[2] Beaumont Hlth Syst, Dept Internal Med, Royal Oak, MI USA
[3] Beaumont Hlth Syst, Dept Nephrol, Royal Oak, MI USA
来源
关键词
Proteinuria; Focal segmental glomerulosclerosis; Lupus nephritis; Chronic kidney disease; ESRD; THROMBOTIC MICROANGIOPATHY; ERYTHEMATOSUS; GLOMERULOPATHY; VARIANTS; APOL1; ALLELES; DISEASE;
D O I
10.1159/000510840
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Lupus nephritis (LN) and the collapsing variant of focal segmental glomerulosclerosis (cFSGS) are separate histologic diagnoses that are generally thought to have separate etiologies. We describe the presentation of a 20-year-old African American female with advanced renal failure (creatinine 7.16 mg/dL), nephrotic-range proteinuria, and a 30-pound weight loss. Renal biopsy demonstrated class 2 and 3 LN as well as cFSGS. A review of the current literature demonstrates that the dual diagnosis of LN and cFSGS may not be as rare as previously understood. Whether the presence of one of these pathophysiologic processes predisposes a patient to the development of the other, or whether genetic variation increases the risk for development of both conditions, remains unclear. Currently there is no standard therapy to manage these patients, and overall renal prognosis is poor.
引用
收藏
页码:16 / 25
页数:10
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