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| 막증식성 사구체신염으로 발현된 원발성 항인지질 증후군 1예 (A Case of Primary Antiphospholipid Syndrome Presented with Membranoproliferative Glomerulonephritis pattern) |
| 김재훈, 김창수, 오동호, 최병렬, 도준형, 손호상, 안기성, 김용진 (Jae Hoon Kim, Chang Soo Kim, Dong Ho Oh, Byung Ryul Choi, Joon Hyung Doh, Ho Sang Sohn, Ki Sung Ahn and Yong Jin Kim) |
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| Abstract |
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Though the renal abnormality is usually accompanied in the patient with antiphospholipid syndrome, it is not frequent that the symptoms of antiphospholipid syndrome are confined to kidney. We experienced a case of 40-year-old woman suffered from intermittently developed nephrotic range proteinuria combined with generalized edema during last 10 years. She had no past history of thrombosis, spontaneous abortion, or symptoms related to SLE. Laboratory findings revealed that she had nephrotic syndrome. Her antinuclear antibody was negative, but her serum antiphospholipid IgG antibody level was 32 GPL IU. In the renal biopsy specimen, half of the glomeruli showed global sclerosis and remaining glomeruli showed chronic thrombotic microangiopathy and membranoproliferative glomerulonephritis without immune deposit. Combined therapy with steroid and aspirin improve the amount of proteinuria, and she is free from edema without deterioration of renal function during follow up. Though this case lacked the typical symptoms of antiphospholipid syndrome, her glomerulonephritis presented with membranoproliferative pattern may be associated with it. We report this case with a review of literatures. |
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