Parallel improvement of chorea and antiphospholipid autoimmunity during combination therapy with hydroxychloroquine, belimumab and glucocorticoids in systemic lupus erythematosus [0.03%]
羟氯喹、贝利尤单抗和糖皮质激素联合治疗系统性红斑狼疮改善舞蹈症和抗磷脂-auto免疫的并行研究
Ryoko Asano,Hiroki Maesaka,Satoshi Yamaguchi et al.
Ryoko Asano et al.
Chorea is a movement disorder observed in 1-2% of systemic lupus erythematosus (SLE) cases. Treatment options include anticonvulsants, dopamine antagonists, antiplatelets, anticoagulants, and immunosuppressants such as cyclophosphamide; how...
Reversal of chronic arterial stenosis with biologic therapy including tocilizumab in Takayasu arteritis [0.03%]
生物制剂治疗包括托珠单抗逆转Takayasu动脉炎慢性动脉狭窄
Chisako Kitayama,Tsuyoshi Shirai,Tokio Katakura et al.
Chisako Kitayama et al.
Biologic agents have demonstrated efficacy in the treatment of refractory Takayasu arteritis (TAK). Although vascular stenosis is a common manifestation in the chronic phase of TAK, evidence on the effects of biologic therapy on established...
Delayed Diagnosis of Psoriatic Arthritis Presenting with Infection-like Finger Inflammation: A Case Report [0.03%]
延迟诊断的银屑病关节炎以类似感染的指炎为首发表现：病例报告
Sho Takahashi,Yasuhiro Kiyota,Takuji Iwamoto et al.
Sho Takahashi et al.
Psoriatic arthritis is a chronic inflammatory disease associated with psoriasis, and its diagnosis can be challenging owing to nonspecific symptoms, absence of reliable biomarkers, and occasional delay in skin manifestations. Herein, we rep...
Navigating Clinical Overlap: A Case of Polyarteritis Nodosa in the Setting of Antiphospholipid Syndrome [0.03%]
重叠综合征的诊断和治疗：抗磷脂综合症合并多动脉炎结节征病例报告及文献回顾
Anushri Nimbvikar,Ryan Tudino,Carmen Fahlen et al.
Anushri Nimbvikar et al.
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis of medium-sized arteries, often challenging to differentiate from other autoimmune and thrombotic disorders due to overlapping clinical features. This case-based literature rev...
Is it a secondary cause of vasculitis or a mimic? A case of retinal vasculopathy with cerebral leukoencephalopathy [0.03%]
视神经血管炎伴发脑白质病是一种视网膜血管炎还是类似疾病？报告一例RPCVL临床诊断案例
Sidar Çöpür,Yunus Emre Senturk,Yunus Baran Kok et al.
Sidar Çöpür et al.
Central nervous system involvement in vasculitis disorders, either primary or secondary, is a heterogeneous and challenging area in rheumatology clinical in terms of both diagnostics and therapeutics. Retinal vasculopathy with cerebral leuk...
Thrombotic microangiopathy in a patient with anti-signal recognition particle antibody-positive immune-mediated necrotizing myopathy: a case report [0.03%]
抗信号识别颗粒抗体阳性自身免疫性坏死性肌炎合并血栓性微血管病一例报告
Takao Kodera,Kenichi Akiyama,Motoki Kubota et al.
Takao Kodera et al.
Thrombotic microangiopathy (TMA) is a rare but life-threatening complication in idiopathic inflammatory myopathies. Although TMA has been increasingly recognized in anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive de...
Pancytopenia and splenomegaly as uncommon manifestations in a patient with immunoglobulin G4-related disease [0.03%]
免疫球蛋白G4相关疾病患者的少见表现——全血细胞减少和脾大
Kojiro Ikeda,Shunichiro Hanai,Soichiro Kubota et al.
Kojiro Ikeda et al.
Hematological manifestations of immunoglobulin (Ig)G4-related disease (IgG4-RD) are atypical, and few studies have addressed cytopenia in this condition. We present here a case of IgG4-RD with marked pancytopenia and splenomegaly in the abs...
Aortic graft invasion into duodenum as an atypical pathergy phenomenon in vascular Behçet's disease [0.03%]
血管性贝赫切特病中主动脉移植物侵犯十二指肠作为不典型的病理现象
Erdem Bektas,Gultekin Saday,Umut Celik et al.
Erdem Bektas et al.
Behçet's disease (BD) is a multisystemic inflammatory disorder that can affect vessels of all sizes, often leading to significant vascular morbidity. We present the case of a 37-year-old man with BD who developed a rare and severe postoper...
Bilateral orbital masses caused by IgG4-expressing MALT lymphoma in the right side and IgG4-related ophthalmic disease in the left side: A case report [0.03%]
右侧IgG4相关黏膜相关淋巴组织(MALT)淋巴瘤和左侧IgG4相关眼病所致的双侧 orbital 肿块：一例报告
Yasuto Araki,Yuko Mishima,Taketo Yamada et al.
Yasuto Araki et al.
A 60-year-old Japanese man developed a protruding right eye. He underwent a magnetic resonance imaging (MRI) scan, which revealed a right orbital mass. The serum immunoglobulin G4 (IgG4) level was elevated and IgG4+ plasma cells were observ...
Katherine E Moore,Gabriella Venter,John P Slavotinek et al.
Katherine E Moore et al.
Aortitis is a rare but critical manifestation of systemic inflammatory disease, most commonly associated with large-vessel vasculitides such as Takayasu arteritis and giant cell arteritis. When accompanied by multiorgan inflammation and fib...