Intra-articular osteoid osteoma at the elbow mimicking arthritis: a case report.

IF 0.5 4区 医学 Q4 ORTHOPEDICS
Annals of Joint Pub Date : 2022-04-15 eCollection Date: 2022-01-01 DOI:10.21037/aoj-21-27
Ryuichi Fukuda, Masatake Matsuoka, Daisuke Kawamura, Takeshi Endo, Hiromi Kanno-Okada, Atsushi Urita, Yuichiro Matsui, Tomohiro Onodera, Norimasa Iwasaki
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引用次数: 0

Abstract

Osteoid osteomas are benign, typically intracortical lesions most often affecting the diaphysis of long bones. Nocturnal pain and characteristic symptoms that are relieved by administration of non-steroidal anti-inflammatory drugs (NSAIDs) are present and can help in the diagnosis of osteoid osteoma. We report a case of 18-year-old boy with an osteoid osteoma in the olecranon fossa with an atypical clinical manifestation. The initial manifestation was arthritis-like symptoms such as local heat, motion pain rather than pain at rest, and limited range-of-motion. Notably, NSAIDs were not effective at all for relieving his symptoms. Magnetic resonance imaging showed bone marrow edema around the elbow joint. The symptoms were resistant to conservative treatments, and thus, surgical resection was required. Histopathological examination showed that the lesion consisted of woven bones and osteoid tissues that anastomosed with each other. Combined with a tumor size that was less than 2 cm, clinicopathologically, the tumor was diagnosed as an osteoid osteoma. The pain was immediately relieved after the operation, and range-of-motion recovered at 2 months postoperatively. At 1 year after the surgery, the patient did not exhibit recurrence of the tumor or exacerbation of elbow pain and had a full range of elbow motion. Osteoid osteoma should be considered for the differential diagnosis of arthritis of the elbow in patients who are adolescents and young adults, which is the peak age of onset for osteoid osteoma.

模拟关节炎的肘关节内骨样骨瘤1例
骨样骨瘤是一种典型的皮质内良性病变,最常见于长骨的干骺端。夜间疼痛和特征性症状在服用非甾体抗炎药(NSAID)后可缓解,有助于骨样骨瘤的诊断。我们报告了一例临床表现不典型的 18 岁男孩肩胛窝骨样骨瘤病例。最初表现为关节炎样症状,如局部发热、运动疼痛而非休息时疼痛,以及活动范围受限。值得注意的是,非甾体抗炎药对缓解他的症状完全无效。磁共振成像显示肘关节周围骨髓水肿。这些症状对保守治疗无效,因此需要进行手术切除。组织病理学检查显示,病变由相互吻合的编织骨和骨组织组成。结合肿瘤小于 2 厘米的大小,临床病理诊断该肿瘤为骨样骨瘤。术后疼痛立即缓解,术后 2 个月活动范围恢复。术后 1 年,患者的肿瘤没有复发,肘部疼痛也没有加重,肘部活动范围完全恢复。在鉴别诊断青少年肘关节炎时,应考虑骨样骨瘤,因为青少年是骨样骨瘤的高发年龄。
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来源期刊
Annals of Joint
Annals of Joint ORTHOPEDICS-
CiteScore
1.10
自引率
-25.00%
发文量
17
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