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银屑病甲-厚皮骨膜病(POPP):一例成功接受 IL-17 阻断治疗的病例报告,并对其特征、发病机制和治疗进行文献复习。

Psoriatic onycho-pachydermo periostitis (POPP): a case report treated successfully with IL-17 blockade and a literature review on characteristics, pathogenesis, and treatment.

机构信息

Department of Rheumatology, 424 General Army Hospital, Ring Road N. Efkarpias, 564 03, Thessaloniki, Greece.

Department of Radiology, 424 General Army Hospital, Thessaloniki, Greece.

出版信息

Clin Rheumatol. 2021 Nov;40(11):4749-4757. doi: 10.1007/s10067-021-05729-0. Epub 2021 Apr 8.

Abstract

Psoriatic onycho-pachydermo periostitis (POPP) is characterized by psoriatic onychodystrophy, connective tissue thickening, and periostitis of the distal phalanges (DPs), producing a drumstick-like deformity. Our aim was to present the first case of POPP treated successfully with an IL-17 inhibitor, perform a literature review of its characteristics and treatment, and explore the possible pathogenesis. We conducted a systematic review of previously presented POPP cases. We present a patient with methotrexate (MTX)-resistant treatment POPP, who had significant resolution of symptoms and inflammatory lesions on post-treatment MRI with secukinumab 150 mg. We also identified 31 cases of POPP (27 males; mean age 44.9 years) in the literature review. There was great toe involvement in 24 cases, and distal interphalangeal (DIP) involvement in 14 cases, with frequent radiographically evident damage. Seventeen of 31 patients received systematic treatment other than biologics, mostly MTX, with no satisfactory results. Anti-TNF agents were used successfully in 5 cases, mostly after disease modifying anti-rheumatic drug (DMARD) failure. Imaging studies in nail psoriasis and DIP psoriatic arthritis have shown an anatomical link among the nail, the DP bone, and the DIP joint entheses, suggesting that POPP may be a subtype of nail disease with excessive involvement of DP tissues (nail, soft tissue, enthesis, and bone). IL-17 inhibition could be an alternative therapeutic option in DMARD-resistant cases of POPP. Conventional treatment achieves modest success, but anti-TNF agents appear to be much more effective. Based on imaging studies, POPP may be a particular subtype of nail disease.

摘要

银屑病甲-厚皮骨膜病(POPP)的特征为银屑病甲营养不良、结缔组织增厚和末节指骨骨膜炎,导致类似鼓槌样的畸形。我们的目的是报告首例成功应用白介素-17(IL-17)抑制剂治疗的 POPP 病例,对其特征和治疗进行文献复习,并探讨可能的发病机制。我们对已发表的 POPP 病例进行了系统回顾。我们报告了 1 例甲氨蝶呤(MTX)耐药的 POPP 患者,在接受司库奇尤单抗 150mg 治疗后,症状和炎症病变在 MRI 上得到显著缓解。我们还在文献复习中确定了 31 例 POPP 病例(27 例男性;平均年龄 44.9 岁)。24 例有大脚趾受累,14 例有远侧指间关节(DIP)受累,常伴有影像学可见的损伤。31 例患者中有 17 例接受了除生物制剂以外的系统治疗,大多数为 MTX,但结果并不理想。5 例成功应用了抗 TNF 药物,大多在疾病修饰抗风湿药物(DMARD)失败后。在指甲银屑病和 DIP 银屑病关节炎的影像学研究中,指甲、末节指骨骨和 DIP 关节附着点之间存在解剖学联系,提示 POPP 可能是一种指甲疾病的亚型,末节指骨组织(指甲、软组织、附着点和骨)过度受累。在 DMARD 耐药的 POPP 病例中,IL-17 抑制可能是一种替代治疗选择。常规治疗取得了一定的疗效,但抗 TNF 药物似乎更有效。基于影像学研究,POPP 可能是一种特殊的指甲疾病亚型。

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