Unusual Presentation of Spinal Osteoid Osteoma: A Case Report.

Mehmet Erkilinc
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Abstract

Introduction: Osteoid osteoma (OO) is a benign osteogenic tumor that most commonly affects long bones, accounting for 2-3% of primary bone tumors. Spinal involvement is relatively rare, representing 6-20% of cases, with the lumbar spine being the most frequently affected region. Typical spinal OO presents with painful scoliosis and nocturnal pain relieved by non-steroidal anti-inflammatory drugs (NSAIDs). However, atypical presentations may occur when lesions are located adjacent to neural structures, leading to radicular symptoms and poor NSAID response. This case report describes an unusual presentation of OO in the L4 superior articular process, manifesting with back and leg pain, minimal NSAID responsiveness, and nerve root irritation.

Case report: A 17-year-old male presented with a 6-month history of back and leg pain, fluctuating between 3/10 and 7/10 in severity, with associated numbness in the L3 dermatome. Examination revealed painful paraspinal palpation and a positive straight leg raise on the right side, without motor weakness or reflex abnormalities. Magnetic resonance imaging demonstrated non-specific inflammatory changes, whereas computed tomography (CT) confirmed a 9 × 9 mm nidus in the right superior articular process of L4. Given the lesion's proximity to neural structures, radiofrequency ablation was deemed unsafe, and surgical excision was performed. The patient underwent open resection of the nidus with preservation of the inferior facet joint. Immediate post-operative resolution of leg pain was noted, and at 3-month follow-up, the patient reported complete resolution of both back and leg pain, with no recurrence of symptoms.

Conclusion: This case highlights an atypical presentation of spinal OO, characterized by radicular symptoms and poor NSAID response due to nerve root inflammation. It underscores the importance of considering OO in the differential diagnosis of adolescent back and leg pain, even in the absence of classic features. CT imaging remains essential for definitive diagnosis, and surgical excision provides safe and effective treatment when minimally invasive options are contraindicated by lesion proximity to neural structures.

脊柱骨样骨瘤的异常表现:1例报告。
骨样骨瘤(Osteoid osteoma, OO)是一种最常见于长骨的良性成骨肿瘤,占原发性骨肿瘤的2-3%。脊柱受累相对罕见,占病例的6-20%,腰椎是最常见的受累区域。典型的脊柱OO表现为疼痛的脊柱侧凸和夜间疼痛,非甾体抗炎药(NSAIDs)缓解。然而,当病变位于神经结构附近时,可能会出现不典型的表现,导致神经根性症状和较差的非甾体抗炎药反应。本病例报告描述了一个不寻常的腰4上关节突OO的表现,表现为背部和腿部疼痛,轻微的非甾体抗炎药反应和神经根刺激。病例报告:一名17岁男性,有6个月的背部和腿部疼痛史,严重程度在3/10到7/10之间波动,并伴有L3皮节麻木。检查显示脊椎旁触诊疼痛,右侧直腿抬高,无运动无力或反射异常。磁共振成像显示非特异性炎症改变,而计算机断层扫描(CT)证实L4右侧上关节突有9 × 9 mm病灶。鉴于病变靠近神经结构,射频消融被认为是不安全的,并进行手术切除。患者行病灶开放切除术,保留下关节突关节。术后腿部疼痛立即得到缓解,在3个月的随访中,患者报告背部和腿部疼痛完全缓解,无症状复发。结论:该病例突出了脊柱OO的非典型表现,其特征是神经根症状和神经根炎症引起的非甾体抗炎药反应差。它强调了在青少年背部和腿部疼痛的鉴别诊断中考虑OO的重要性,即使在没有经典特征的情况下。CT成像仍然是明确诊断的必要条件,当病变靠近神经结构禁忌微创选择时,手术切除提供了安全有效的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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