青少年皮肌炎中钙质沉着的影像学评价:一篇叙述性综述。

IF 2.3 3区 医学 Q1 PEDIATRICS
Belina Y Yi, Jessica Perfetto, Evin Rothschild, Kelly Rouster-Stevens, Amanda Robinson, Kathryn Cook, Delaney D Ding, Andrea Eagle Child, Ovgu Kul Cinar, Barbara Limbach, Charalampia Papadopoulou, Lesley Ann Saketkoo, Adam Schiffenbauer, Heinrike Schmeling, Antonia Valenzuela, Susan Shenoi, Dawn M Wahezi
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引用次数: 0

摘要

钙质沉着症是青少年和成人特发性炎性肌病的一种严重表现,可导致疼痛、活动范围受限、毁容和感染。它在青少年特发性炎性肌病中更常见,特别是在青少年皮肌炎(JDM)中。钙质沉着症可在皮肤表面可见,但也可出现在肌肉和内脏器官中,因此在没有影像学检查的情况下很难进行彻底评估。在这篇叙述性综述中,我们讨论了用于评估jdm相关钙质沉着症的不同成像方式,包括x射线、计算机断层扫描(CT)、磁共振成像(MRI)和超声(US)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Imaging assessment of calcinosis in juvenile dermatomyositis: a narrative review.

Imaging assessment of calcinosis in juvenile dermatomyositis: a narrative review.

Imaging assessment of calcinosis in juvenile dermatomyositis: a narrative review.

Imaging assessment of calcinosis in juvenile dermatomyositis: a narrative review.

Calcinosis is a severe manifestation of juvenile and adult idiopathic inflammatory myopathies, which can lead to pain, limited range of motion, disfigurement, and infection. It is more common in juvenile idiopathic inflammatory myopathies, especially in juvenile dermatomyositis (JDM). Calcinosis can be visible on cutaneous surfaces, although can also present in muscles and internal organs, making a thorough assessment difficult without imaging modalities. In this narrative review, we discuss different imaging modalities used in evaluating JDM-associated calcinosis including X-ray, computed tomography (CT), magnetic resonance imaging (MRI), and ultrasound (US).

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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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