Sousa Rui, Resende Ana Flávia, Pinto Luís Barbosa, Lages Marta, Negrão Luísa, Simões Nuno
Viseu Dão-Lafões Local Health Unit - Av. Rei Dom Duarte, 3504-509 Viseu.
J Orthop Case Rep. 2025 Feb;15(2):136-140. doi: 10.13107/jocr.2025.v15.i02.5258.
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.
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.
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.
股神经病变是一种罕见病症,通常由股神经受压引起。虽然它在抗凝治疗的患者中常因腰大肌血肿而出现,但无明显外伤或凝血障碍的自发性髂肌血肿极为罕见。本病例报告详细介绍了一名青少年患者自发性髂肌血肿的发生及处理情况。此类病例鲜有报道,因此这份记录对于增进临床认识和管理策略至关重要。
一名16岁白种男性,无重大病史,出现大腿肌肉萎缩、左下肢力量减弱以及一个月内负重能力逐渐丧失的症状。患者自述无外伤史。临床检查发现股神经分布区域感觉减退,股四头肌力量明显减弱。包括磁共振成像在内的影像学检查发现左髂肌深部有一梭形肿块,与包膜下血肿相符。患者接受了休息和止痛药物的保守治疗,随后进行了物理康复。随访评估显示肌肉营养状况和负重能力逐渐改善,1年后股神经传导完全恢复。
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,即使在无外伤或抗凝治疗的情况下。该报告突出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,特别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中保持警惕以预防长期并发症的必要性。通过详细描述这种不寻常的表现,该报告旨在增进对类似病例的理解和治疗策略。