Suppr超能文献

解析舒尔曼综合征:一名儿科患者罕见的嗜酸性筋膜炎病例,其MRI显示筋膜异常

Unraveling Shulman's syndrome: A rare case of eosinophilic fasciitis in a pediatric patient with fascial abnormalities on MRI.

作者信息

Ihssan Hadj Hsain, Sara Ezzaky, Kaoutar Maslouhi, Chailmae Lahlou, Salma Marrakchi, Nazik Allali, Latifa Chat, Siham El Haddah

机构信息

Departement of radiology HER, University Mohammed V Rabat, Rabat, Morocco.

出版信息

Radiol Case Rep. 2025 Jan 10;20(3):1760-1765. doi: 10.1016/j.radcr.2024.10.123. eCollection 2025 Mar.

Abstract

We report the case of a 15-year-old girl who presented with a 2-month history of severe fatigue and rapidly worsening myalgia. Biological tests revealed hypereosinophilia and an inflammatory syndrome. MRI showed increased signal intensity in the superficial and deep aponeurotic layers on T2-weighted images, with moderate fascia enhancement after contrast administration. A muscle biopsy of the arm was performed, revealing an accumulation of eosinophils in the muscle aponeuroses. Eosinophilic fasciitis (EF) is a rare connective tissue disorder characterized by inflammation of the fascia, leading to skin thickening and limb pain. While it predominantly affects adults, pediatric cases are rare, making diagnosis challenging due to its overlap with other fibrotic diseases.

摘要

我们报告了一名15岁女孩的病例,她有2个月的严重疲劳史,且肌痛迅速加重。生物学检查显示嗜酸性粒细胞增多和炎症综合征。磁共振成像(MRI)显示在T2加权图像上,浅、深腱膜层信号强度增加,注射造影剂后筋膜有中度强化。对其手臂进行了肌肉活检,结果显示在肌肉腱膜中有嗜酸性粒细胞聚集。嗜酸性筋膜炎(EF)是一种罕见的结缔组织疾病,其特征是筋膜炎症,导致皮肤增厚和肢体疼痛。虽然它主要影响成年人,但儿科病例很少见,由于其与其他纤维化疾病有重叠,因此诊断具有挑战性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5773/11774640/0acba501bd15/gr1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验