Case Report: Scleroderma Renal Crisis Presenting as Thrombotic Microangiopathy

被引:0
作者
Ugur, Mehmet Can [1 ]
Ekinci, Ferhat [1 ]
Karadeniz, Tugba [2 ]
Gram, Elif [1 ]
Colak, Hulya [3 ]
Ceylan, Cengiz [4 ]
Akar, Harun [1 ]
机构
[1] Izmir Tepecik Educ & Res Hosp, Dept Internal Med, Izmir, Turkey
[2] Izmir Tepecik Educ & Res Hosp, Dept Pathol, Izmir, Turkey
[3] Izmir Tepecik Educ & Res Hosp, Dept Nephrol, Izmir, Turkey
[4] Izmir Tepecik Educ & Res Hosp, Dept Hematol, Izmir, Turkey
来源
TURKISH NEPHROLOGY DIALYSIS AND TRANSPLANTATION JOURNAL | 2016年 / 25卷
关键词
Scleroderma; Renal crisis; Thrombotic microangiopathy; Hemodialysis;
D O I
10.5262/tndt.2016.12
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
Scleroderma is a systemic autoimmune disease of unknown origin characterized by excessive deposition of collagen and other connective tissue macromolecules in multiple organs. It can cause thrombotic microangiopathy. Scleroderma renal crisis is a major complication of this disorder. We aimed to present a case that presented with thrombotic microangiopathy findings and was diagnosed as scleroderma renal crisis. A 56-year-old female patient presented with hypertension and thrombotic microangiopathy signs. After examination and renal biopsy, scleroderma renal crisis with thrombotic microangiopathy was diagnosed. A routine hemodialysis program and an angiotensin converting enzyme inhibitor was started Scleroderma renal crisis should be kept in mind in patients presenting with malignant hypertension and thrombotic microangiopathy.
引用
收藏
页码:71 / 74
页数:4
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