Sconza Cristiano, Coletta Francesco, Magarelli Nicola, D'Agostino Maria Cristina, Egan Colin Gerard, Di Matteo Berardo, Respizzi Stefano, Mazziotti Gherardo
Department of Rehabilitation, IRCCS Humanitas Research Hospital, Milan, Italy.
Department of Biomedical Sciences, Humanitas University, Milan, Italy.
SAGE Open Med Case Rep. 2022 Feb 15;10:2050313X211067617. doi: 10.1177/2050313X211067617. eCollection 2022.
Bone marrow edema syndrome is a severely disabling painful condition without a defined treatment and related to pathogenetic mechanisms not yet clearly recognized. We report the case of a 59-year-old post-menopausal woman, affected by bone marrow edema associated with early osteonecrosis of the femoral head with secondary appearance of a rare migrant bone edema of the hip acetabulum. Clinical evaluation and magnetic resonance imaging were used to monitor the outcome of the patient. Pre-treatment clinical evaluation revealed pain upon stepping with the left limb, reduced range of motion of spine and hip, and hip pain during passive rotation. Magnetic resonance imaging showed diffuse signal alteration of the head and neck of the left femur in relation to bone edema, associated with an unclear small cephalic area of the femoral head suggestive of initial osteonecrosis. A further computed tomography scan was performed that did not reveal any alterations in bone profile, interruption of the cortex, or trabecular bone collapse. We immediately started a multimodal conservative treatment administering neridronate (100 mg, intravenously) combined with calcium and vitamin D supplementation and biophysical therapies (magnetotherapy and extracorporeal shockwave therapy). We also instructed the patient not to bear the load on the affected lower limb during standing and walking, using crutches. After 2 months, a notable regression of pain with improvement in mobility was observed. Magnetic resonance imaging revealed complete regression of edema at the head and neck of the femur; however, the new appearance of acetabular bone edema of the ipsilateral acetabular roof was detected. After 4 months, a third magnetic resonance imaging showed the disappearance of the femoral head and acetabular roof defects as well as the complete clinical recovery of the patient. An early diagnosis and intervention are essential to conservatively treat cases of bone marrow edema syndrome.
骨髓水肿综合征是一种严重致残的疼痛性疾病,尚无明确的治疗方法,其发病机制也尚未完全明确。我们报告了一例59岁的绝经后女性病例,该患者患有与股骨头早期骨坏死相关的骨髓水肿,并继发出现罕见的髋臼迁移性骨水肿。通过临床评估和磁共振成像来监测患者的病情转归。治疗前的临床评估显示,患者左下肢行走时疼痛,脊柱和髋关节活动范围减小,被动旋转时髋关节疼痛。磁共振成像显示,左股骨头部和颈部因骨水肿出现弥漫性信号改变,同时股骨头有一个不明确的小区域提示早期骨坏死。进一步的计算机断层扫描未发现骨轮廓改变、皮质中断或小梁骨塌陷。我们立即开始了多模式保守治疗,静脉注射奈立膦酸(100mg),同时补充钙和维生素D,并进行生物物理治疗(磁疗和体外冲击波治疗)。我们还指导患者站立和行走时不要让患侧下肢负重,使用拐杖辅助。2个月后,观察到疼痛明显减轻,活动能力有所改善。磁共振成像显示股骨头部和颈部的水肿完全消退;然而,同侧髋臼顶出现了新的髋臼骨水肿。4个月后,第三次磁共振成像显示股骨头和髋臼顶的缺损消失,患者临床完全康复。早期诊断和干预对于保守治疗骨髓水肿综合征病例至关重要。