是不是关节炎?厚皮性:幼年特发性关节炎的伟大模仿者。

IF 1.4 4区 医学 Q3 RHEUMATOLOGY
ARP Rheumatology Pub Date : 2023-01-01
Ana Bento da Silva, Maria Helena Lourenço, Maria João Gonçalves, Jaime Cunha Branco, Manuela Costa, Ana Filipa Mourão
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引用次数: 0

摘要

在儿童人群中,关节炎是许多风湿性炎症性疾病以及其他皮肤、感染性或肿瘤性疾病的标志。它可能具有相当的破坏性,因此及时识别和治疗这些疾病是至关重要的。然而,关节炎有时会被误认为是其他皮肤或遗传疾病,导致误诊和过度治疗。厚皮畸形是一种罕见的良性手指纤维瘤病,通常表现为双手近端指间关节肿胀,类似关节炎。作者报告了一个12岁的男孩,有一年的双手近端指间关节无痛肿胀史,由于怀疑青少年特发性关节炎而被转介到儿科风湿病科。诊断检查无显著差异,患者在18个月的随访期间无症状。假定诊断为厚皮畸形,鉴于疾病的良性性质和无症状,没有进行治疗。因此,可以安全地将患者从儿科风湿病诊所出院。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Arthritis or maybe not? Pachydermodactyly: the great mimicker of juvenile idiopathic arthritis.

Arthritis in the paediatric population is the hallmark of many rheumatic inflammatory diseases, as well as other cutaneous, infectious, or neoplastic conditions. It can be quite devastating, whereby prompt recognition and treatment of these disorders are essential. However, arthritis can sometimes be mistaken for other cutaneous or genetic conditions leading to misdiagnosis and overtreatment. Pachydermodactyly is a rare and benign form of digital fibromatosis, usually manifested by swelling of the proximal interphalangeal joints of both hands, mimicking arthritis. The authors report a case of a 12-year-old boy with a one-year history of painless swelling of the proximal interphalangeal joints of both hands that was referred to the Paediatric Rheumatology department due to the suspicion of juvenile idiopathic arthritis. The diagnostic work-up was unremarkable, and the patient remained asymptomatic over an 18-month follow-up period. A diagnosis of pachydermodactyly was assumed and no treatment was introduced, given the benign nature of the disorder and absence of symptoms. Therefore, it was possible to safely discharge the patient from the Paediatric Rheumatology clinic.

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