混合性结缔组织病的肾脏表现

IF 0.1 Q4 MEDICINE, GENERAL & INTERNAL Journal of the Scientific Society Pub Date : 2024-03-14 DOI:10.4103/jss.jss_74_20
Shalini Ashok, Meenakshi Kalyan, Vamsavardhan Reddy, S. Sumangala
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摘要

一名年轻女性因面部浮肿、双下肢浮肿 3 个月、腹部胀痛、用力时呼吸困难 1 个月就诊,有高血压和甲状腺功能减退病史,并接受正规治疗。一般体格检查时,患者面色苍白、双侧点状水肿、心动过速,血压为 190/100 mmHg。腹部检查发现腹胀。呼吸和心血管系统正常。眼底镜检查发现 1 级乳头水肿,其他神经系统检查无异常。检查结果显示,患者患有正常红细胞性贫血,血清肌酐为 1.6 毫克/分升,低白蛋白血症;尿液 R/E 显示大量蛋白尿;抗 U1 核糖核蛋白颗粒抗体呈阳性。二维超声心动图显示轻度同心左心室肥厚和轻度心包积液。腹部超声波检查显示双侧肾实质病变和中度腹水。肾活检显示弥漫性增生性肾小球肾炎和狼疮性肾炎 IV 级。在混合性结缔组织病中,以肾脏表现为首发症状非常罕见
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Renal Manifestation of Mixed Connective Tissue Disease
A young female presented with facial puffiness and swelling in both lower limbs for 3 months, distension of the abdomen, and breathlessness on exertion for 1 month with a history of hypertension and hypothyroid on regular treatment. On general physical examination, there were pallor, bilateral pitting edema, tachycardia, and blood pressure of 190/100 mmHg. Abdominal examination revealed shifting dullness. Respiratory and cardiovascular systems were normal. Fundoscopy revealed Grade 1 papilledema, and the rest of the neurological examination was unremarkable. Investigations showed normocytic normochromic anemia, serum creatinine of 1.6 mg/dl, and hypoalbuminemia; urine R/E showed significant proteinuria; and anti-U1 ribonucleoprotein particle antibodies were positive. Two-dimensional echocardiography showed mild concentric left ventricular hypertrophy and mild pericardial effusion. Ultrasonography abdomen showed bilateral renal parenchymal disease and moderate ascites. Renal biopsy revealed diffuse proliferative glomerulonephritis and lupus nephritis Class IV. Renal manifestation is very rare in mixed connective tissue disease as an initial presentation
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来源期刊
Journal of the Scientific Society
Journal of the Scientific Society MEDICINE, GENERAL & INTERNAL-
自引率
33.30%
发文量
19
审稿时长
36 weeks
期刊最新文献
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