Coexistence of Rheumatoid Arthritis, Systemic Lupus Erythematosus, Sjogren Syndrome, Antiphospholipid Syndrome, and Ankylosing Spondylitis.

Case Reports in Rheumatology Pub Date : 2021-08-10 eCollection Date: 2021-01-01 DOI:10.1155/2021/8491717
Moshiur Rahman Khasru, Md Abu Bakar Siddiq, Kazi Mohammad Sayeeduzzaman, Tangila Marzen, Abul Khair Mohammad Salek
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引用次数: 2

Abstract

A 37-year-old Bangladeshi woman presented with low back and several joints pain and swelling for months together; there was significant morning stiffness for more than two hours. Repeated abortions, dry eye, hair fall, photosensitivity, and oral ulcer were the additional complaints. Clinical examination unveiled asymmetrical peripheral and both sacroiliac joint tenderness, positive modified Schober's test, and limited chest expansion. Schirmer's test was positive. The history of rheumatoid arthritis (RA) and ankylosing spondylitis (AS) among 1st-degree relatives was also significant. Biochemical analysis revealed pancytopenia, raised erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP), and mild microscopic proteinuria. The patient was seropositive for rheumatoid factor (RF), antibodies against cyclic citrullinated peptides (anti-CCP), antinuclear antibody (ANA), anti-Sm antibody, anti-Sjögren's-syndrome-related antigen A and B (anti-SSA/SSB), antiphospholipid (aPL-IgG/IgM), and HLA B27; however, serum complement (C3 and C4) levels were normal. Basal cortisol level measured elevated. Besides, X-ray and MRI of lumbosacral spines demonstrated sacroiliitis. There was radiological cardiomegaly, echocardiography unveiled atrial regurgitation, and ascending aorta aneurysm. Based on the abovementioned information, RA, AS, and systemic lupus erythematosus (SLE) have been diagnosed. Moreover, the patient developed Sjogren's syndrome (SS), antiphospholipid lipid syndrome (APS), Cushing syndrome, ascending aorta aneurysm, and atrial regurgitation. Her disease activity score for RA (DAS28), DAS for AS (ASDAS), SLE disease activity index (SLEDAI), and Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) scores were 3.46, 2.36, 23, and 5, respectively. The patient received hydroxychloroquine (200 mg daily), pulsed cyclophosphamide, prednisolone (20 mg in the morning), and naproxen 500 mg (twice daily). To our best knowledge, this is the first report documenting RA, AS, and SLE with secondary SS and APS.

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类风湿关节炎、系统性红斑狼疮、干燥综合征、抗磷脂综合征和强直性脊柱炎的共存。
一名37岁的孟加拉国妇女,连续数月出现腰背部和多个关节疼痛和肿胀;有明显的早晨僵硬超过两个小时。反复流产、干眼、脱发、光敏性和口腔溃疡是附加的主诉。临床检查发现不对称外周及双骶髂关节压痛,修正肖伯氏试验阳性,胸部扩张受限。席默的检测结果呈阳性。一级亲属中类风湿关节炎(RA)和强直性脊柱炎(AS)病史也具有显著性。生化分析显示全血细胞减少,红细胞沉降率(ESR)和c反应蛋白(CRP)升高,显微镜下轻度蛋白尿。患者血清类风湿因子(RF)、抗环瓜氨酸肽抗体(抗ccp)、抗核抗体(ANA)、抗sm抗体、anti-Sjögren综合征相关抗原A和B(抗ssa /SSB)、抗磷脂(aPL-IgG/IgM)、HLA B27阳性;血清补体(C3和C4)水平正常。基础皮质醇水平升高。腰骶棘x线及MRI表现为骶髂炎。胸片示心脏肿大,超声心动图示心房返流,升主动脉动脉瘤。基于上述信息,RA, AS和系统性红斑狼疮(SLE)已被诊断。此外,患者还出现干燥综合征(SS)、抗磷脂脂质综合征(APS)、库欣综合征、升主动脉动脉瘤和心房反流。她的RA疾病活动性评分(DAS28)、AS疾病活动性评分(ASDAS)、SLE疾病活动性指数(SLEDAI)和系统性狼疮国际合作诊所/美国风湿病学会(SLICC/ACR)评分分别为3.46、2.36、23和5。患者接受羟氯喹(每日200 mg)、脉冲环磷酰胺、强的松龙(早晨20 mg)、萘普生500 mg(每日2次)。据我们所知,这是第一份记录RA、AS和SLE伴继发性SS和APS的报告。
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