Bicipital synovial cyst in poly-articular juvenile idiopathic arthritis

K. Bouayed, Fenna El Founti, A. Sakhi, R. Taoussi, Z. Qechchar, N. Mikou
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引用次数: 1

Abstract

Background: Large synovial cysts are rare in juvenile idiopathic arthritis ( JIA). They are usually located in popliteal area. Bicipital cyst is uncommon and has been described in systemic onset of JIA during an inflammatory attack. We describe the presentation and clinical course of bicipital synovial cyst occurring in patient with polyarticular subtype of JIA. In our knowledge, it’s the first case reported. Case presentation: Our patient had an active disease with high level of biological inflammation. After ruling out the infectious origin of the cyst, the diagnosis was confirmed by ultrasonography revealing a liquid nature of the formation and magnetic resonance imaging showing the continuity between the shoulder’s joint effusion and the cyst. A complete resolution was obtained 4 weeks after control inflammation using high dose of anti inflammatory drugs (prednisone 1mg/kg/d, indomethacin 3 mg/kg/d). Conclusion: Bicipital cyst is an unusual condition of JIA, extremely rare in polyarticular form. His etiology remains poorly understood. Our Patient had a high level of biological inflammation as in systemic subtype. The diagnosis is confirmed by ultrasonography. Magnetic resonance imaging may be helpful in case of doubt. The treatment is no specific and based on the control of the disease activity. Even though bicipital cyst is rare manifestation of JIA, it should be considered as a complication of active disease related to inflammatory phenomena. *Correspondence to: Bouayed Kenza, Department of Pediatric Rheumatology, A. Harouchi University Children’s Hospital, Ibn Rochd, Mo-hamed El Fidouzi Street ex Jenner, Kergomard Street, Bay View Residence, A3, Ain Diab, Casablanca, Morocco, 20 052, Tel: +212 661 31 07 74; E-mail: bouayedkenza@ hotmail.com
多关节幼年特发性关节炎的二头滑膜囊肿
背景:大滑膜囊肿在幼年特发性关节炎(JIA)中是罕见的。它们通常位于腘窝区。肱二头囊肿是罕见的,并已被描述为全身性发作的JIA在炎症发作。我们描述了发生在JIA多关节亚型患者的头滑膜囊肿的表现和临床过程。据我们所知,这是首例报告病例。病例介绍:我们的病人有一个活动性疾病与高水平的生物炎症。在排除了囊肿的感染性来源后,超声检查证实了诊断,显示囊肿的液体性质,磁共振成像显示肩关节积液和囊肿之间的连续性。大剂量抗炎药物(强的松1mg/kg/d,吲哚美辛3mg /kg/d)控制炎症4周后完全消退。结论:肱二头囊肿是一种少见的JIA,在多关节形式下极为罕见。他的病因尚不清楚。我们的病人有高水平的全身性炎症。超声检查证实了诊断。如果有疑问,磁共振成像可能会有所帮助。治疗无特异性,以控制疾病活动为基础。虽然二头囊肿是JIA的罕见表现,但应考虑为与炎症现象相关的活动性疾病的并发症。*通信:Bouayed Kenza,儿科风湿病科,A. Harouchi大学儿童医院,Ibn Rochd, Mo-hamed El Fidouzi Street ex Jenner, Kergomard Street, Bay View Residence, A3, Ain Diab,摩洛哥卡萨布兰卡,20052,电话:+212 661 31 07 74;电子邮件:bouayedkenz@hotmail.com
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