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首页> 外文期刊>Medicine. >Inflammatory Arthritis in Patients With Myelodysplastic Syndromes: A Multicenter Retrospective Study and Literature Review of 68 Cases
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Inflammatory Arthritis in Patients With Myelodysplastic Syndromes: A Multicenter Retrospective Study and Literature Review of 68 Cases

机译:骨髓增生异常综合症患者的炎性关节炎:多中心回顾性研究和68例文献复习

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Abstract: We describe the characteristics and outcome of inflammatory arthritis in patients with myelodysplastic syndrome (MDS) in a French multicenter retrospective study. Twenty-two patients with MDS (median age, 77.5 yr [interquartile range, 69–81]; 10 women) were included. Inflammatory arthritis presented as polyarthritis in 17 cases (77%) and with symmetric involvement in 15 cases (68%). At diagnosis, the median disease activity score 28 based on C-reactive protein (DAS28-CRP) was 4.5 [2–6.5]. Two patients had anti-citrullinated protein antibodies (ACPAs), and 1 had radiologic erosions. The median time between the diagnoses of arthritis and MDS was 10 months [6–42], with a median articular symptom duration of 3 months [2–8]. The diagnosis of both diseases was concomitant in 6 cases (27%); arthritis preceded MDS in 12 cases (55%), and occurred after MDS in 4 (18%). While the number of swollen and tender joints significantly decreased during follow-up, as did the median DAS28-CRP (from 4.3 [3.8–4.6] at baseline to 2.9 [1.75–3.3]; p 20 mg/L) in 8 patients (42%). Nevertheless, radiographic progression and new ACPA positivity were not observed during a median follow-up of 29 months [9–76]. While most of the patients were treated with steroids (n = 16) for arthritis, additional treatment was administered in only 4 patients (hydroxychloroquine, n = 2; sulfasalazine [Salazopyrin] and etanercept, n = 1, respectively). Eleven patients died during follow-up from acute myeloid leukemia (n = 5); infections (n = 3); or cerebral bleeding, cardiorespiratory failure, or undetermined cause (n = 1, respectively). Inflammatory arthritis associated with MDS can have various presentations and is often seronegative and nonerosive. Steroids alone are the most common treatment in MDS-associated arthritis, but that treatment is insufficient to control arthritis. Steroid-sparing strategies need to be identified.
机译:摘要:我们在一项法国多中心回顾性研究中描述了骨髓增生异常综合征(MDS)患者的炎症性关节炎的特征和结局。包括22名MDS患者(中位年龄为77.5岁[四分位间距为69-81]; 10名妇女)。炎症性关节炎表现为多发性关节炎17例(77%),对称受累15例(68%)。诊断时,基于C反应蛋白(DAS28-CRP)的疾病活动评分中位数28为4.5 [2–6.5]。 2例患者具有抗瓜氨酸化蛋白抗体(ACPA),1例患有放射侵蚀。诊断关节炎和MDS之间的中位时间为10个月[6–42],中位关节症状持续时间为3个月[2–8]。两种疾病的诊断均伴有6例(27%)。关节炎发生在MDS之前12例(55%),发生在MDS之后4例(18%)。在随访期间,尽管肿胀和触痛的关节数量显着减少,但DAS28-CRP的中位数(从基线时的4.3 [3.8-4.6]降至基线的2.9 [1.75-3.3]; p 20 mg / L)也是如此( 42%)。然而,在中位随访29个月期间未观察到影像学进展和新的ACPA阳性[9-76]。尽管大多数患者因类固醇治疗关节炎(n = 16),但仅对4位患者进行了其他治疗(羟氯喹,n = 2;柳氮磺吡啶[salazopyrin]和依那西普,n = 1)。随访期间有11例患者死于急性髓细胞性白血病(n = 5);感染(n = 3);或脑出血,心肺衰竭或原因不明(分别为n = 1)。与MDS相关的炎性关节炎可以有多种表现,并且通常是血清阴性和非侵蚀性的。单独的类固醇是与MDS相关的关节炎的最常见治疗方法,但这种治疗方法不足以控制关节炎。需要确定类固醇保存策略。

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