Ihssan Hadj Hsain, Sara Ezzaky, Kaoutar Maslouhi, Chailmae Lahlou, Salma Marrakchi, Nazik Allali, Latifa Chat, Siham El Haddah
Departement of radiology HER, University Mohammed V Rabat, Rabat, Morocco.
Radiol Case Rep. 2025 Jan 10;20(3):1760-1765. doi: 10.1016/j.radcr.2024.10.123. eCollection 2025 Mar.
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.
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。