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距骨骨样骨瘤——一种罕见的酷似踝关节关节炎的病例:病例报告

Osteoid Osteoma of Talus - A Rare Occurrence Mimicking Ankle Arthritis: A Case Report.

作者信息

Pai Satvik N, Kumar Mohan M, Vanchi Pravin K, Ravi Raghav

机构信息

Department of Orthopaedic Surgery, Sri Ramachandra Medical College and Research Institute, Chennai, Tamil Nadu, India.

出版信息

J Orthop Case Rep. 2022 Feb;12(2):53-56. doi: 10.13107/jocr.2022.v12.i02.2664.

Abstract

INTRODUCTION

Osteoid osteoma is a benign, bone forming tumor which accounts for nearly 10% of all benign bone tumors. The foot is very rarely involved, with only around 2% of osteoid osteomas being reported to occur in bones of the foot. Osteoid osteoma of the talus could present as symptoms mimicking monoarticular arthritis of the ankle. We present a case of osteoid osteoma occurring in the neck of talus, presenting such a diagnostic dilemma.

CASE REPORT

A 13-year-old male child had complaints of pain and swelling in his right ankle since 1 year. The pain was predominantly aggravated at night and partially relieved by non-steroidal anti-inflammatory drugs. On examination, we found a diffuse, ill-defined, and soft swelling over the anteromedial aspect of the right ankle, which was anterior and inferior to the medial malleolus. The movements at the ankle joint were restricted and painful. Lateral radiograph of ankle revealed a solitary, osteolytic, and circular lesion involving the neck of the talus. Computed tomography (CT) scan showed a well-defined, lucent, and intramedullary lesion with a sclerotic rim in the neck of talus. The child was diagnosed to have osteoid osteoma of the neck of talus. We performed percutaneous CT-guided radiofrequency ablation (RFA) of the lesion. The child had complete relief of pain after the procedure. The child was followed up for 3 years and had no complaints of pain.

CONCLUSION

Osteoid osteoma very rarely occurs in the talus. It can present as monoarticular arthritis involving the ankle joint and requires a high degree of suspicion to be identified. A CT scan remains the most accurate investigation to confirm the diagnosis. We found percutaneous CT-guided RFA to have yielded good outcome without recurrence.

摘要

引言

骨样骨瘤是一种良性成骨肿瘤,占所有良性骨肿瘤的近10%。足部很少受累,据报道仅约2%的骨样骨瘤发生在足部骨骼。距骨骨样骨瘤可能表现出类似踝关节单关节炎的症状。我们报告一例发生在距骨颈部的骨样骨瘤,呈现出这样的诊断困境。

病例报告

一名13岁男性儿童自1年前开始出现右踝疼痛和肿胀。疼痛主要在夜间加重,非甾体类抗炎药可部分缓解。检查时,我们发现右踝前内侧弥漫性、边界不清且质地柔软的肿胀,位于内踝前方和下方。踝关节活动受限且疼痛。踝关节外侧X线片显示距骨颈部有一个孤立的溶骨性圆形病变。计算机断层扫描(CT)显示距骨颈部有一个边界清晰、透亮的髓内病变,伴有硬化边缘。该患儿被诊断为距骨颈部骨样骨瘤。我们对该病变进行了CT引导下经皮射频消融(RFA)。术后患儿疼痛完全缓解。对患儿进行了3年随访,无疼痛主诉。

结论

骨样骨瘤极少发生在距骨。它可表现为累及踝关节的单关节炎,需要高度怀疑才能确诊。CT扫描仍然是确诊的最准确检查方法。我们发现CT引导下经皮RFA取得了良好效果且无复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de7f/9499141/f252acb2179f/JOCR-12-53-g001.jpg

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