- Author:
Eui Chang KIM
1
;
Hyun Suk LEE
;
Yong Seok LIM
;
Jun Ho LEE
;
So Yeon OH
;
Hyun Soon LEE
;
Min Young KIM
Author Information
- Publication Type:Case Report
- Keywords: Lupus nephritis; Glomerulonephritis; Lymphoma; Non-Hodgkin
- MeSH: Biopsy; Creatinine; Drug Therapy; Edema; Glomerulonephritis*; Humans; Immune Complex Diseases; Lupus Erythematosus, Systemic; Lupus Nephritis; Lymphoid Tissue; Lymphoma; Lymphoma, B-Cell, Marginal Zone*; Middle Aged
- From:Korean Journal of Medicine 2016;90(1):50-54
- CountryRepublic of Korea
- Language:Korean
- Abstract: Lupus-like glomerulonephritis is an immune complex disease with features of lupus nephritis in the absence of systemic lupus erythematosus (SLE). We report a 49-year-old man diagnosed with lupus-like glomerulonephritis associated with extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT). He was admitted to the hospital for edema. At admission, the serum creatinine was 2.2 mg/dL and the urine protein level was 3.9 mg/day. A renal biopsy showed features of lupus nephritis with no clinical or serological evidence of SLE. Extranodal marginal zone B-cell lymphoma of MALT was discovered concurrently. After successful chemotherapy, the lupus-like glomerulonephritis and lymphoma entered complete remission.