Rui Sousa, Ana Flávia Resende, Luís Barbosa Pinto, Marta Lages, Luísa Negrão, Nuno Simões
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引用次数: 0

摘要

简介股神经病是一种罕见的疾病,通常是由于股神经受压所致。虽然它通常与腰肌血肿引起的抗凝患者有关,但没有任何明显外伤或凝血障碍的自发性髂骨肌血肿却极为罕见。本病例报告详细介绍了一名青少年患者自发性髂骨肌血肿的发生和处理。此类病例鲜有报道,因此本病例的记录对于加深临床理解和管理策略至关重要:病例报告:一名 16 岁的高加索裔男性患者,无明显病史,一个月来出现大腿肌肉萎缩、左下肢力量减弱,并逐渐丧失负重能力。患者无外伤史。临床检查显示,患者股神经区域感觉减退,股四头肌肌力明显下降。包括磁共振成像在内的影像学检查发现,左侧髂肌深处有一个纺锤形肿块,与包裹性血肿一致。患者接受了休息和止痛的保守治疗,随后进行了物理康复。随访评估显示,患者的肌肉萎缩和负重能力逐渐改善,股神经传导在一年后完全恢复:本病例强调了在股神经病变的鉴别诊断中考虑自发性髂肌血肿的重要性,即使没有外伤或抗凝治疗。该报告强调了进行全面临床评估和影像学检查以确保准确诊断的必要性。它为骨科文献增添了有价值的信息,尤其是在处理股神经病变的罕见表现方面,强调了在监测和随访方面保持警惕以预防长期并发症的必要性。通过详细介绍这种不寻常的表现形式,该报告旨在加深人们对类似病例的理解并改进治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Femoral Neuropathy Secondary to Compression by Spontaneous Iliac Hematoma.

Introduction: Femoral neuropathy is a rare condition typically resulting from compression of the femoral nerve. While it is commonly associated with anticoagulated patients due to psoas hematomas, spontaneous iliacus muscle hematomas without any evident trauma or coagulation disorders are exceedingly uncommon. This case report details the occurrence and management of a spontaneous iliacus muscle hematoma in an adolescent patient. Such cases have been scarcely reported, making this documentation critical for enhancing clinical understanding and management strategies.

Case report: A 16-year-old male of Caucasian ethnicity, with no significant medical history, presented with thigh muscle atrophy, decreased strength in the left lower limb, and progressive loss of weight-bearing capacity over a month. The patient reported no history of trauma. Clinical examination revealed hypoesthesia in the femoral nerve territory and significantly reduced quadriceps muscle strength. Imaging studies, including magnetic resonance imaging, identified a fusiform mass deep to the left iliac muscle, consistent with an encapsulated hematoma. The patient was treated conservatively with rest and analgesics, followed by physical rehabilitation. Follow-up assessments showed progressive improvement in muscle trophism and weight-bearing capacity, with complete recovery of femoral nerve conduction at 1 year.

Conclusion: This case underscores the importance of considering spontaneous iliacus muscle hematomas in the differential diagnosis of femoral neuropathy, even in the absence of trauma or anticoagulation therapy. The report highlights the necessity for thorough clinical evaluation and imaging to ensure accurate diagnosis. It adds valuable information to the orthopedic literature, particularly in managing rare presentations of femoral neuropathy, emphasizing the need for vigilance in monitoring and follow-up to prevent long-term complications. By detailing this unusual presentation, the report aims to enhance the understanding and treatment strategies for similar cases.

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