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肘部酷似关节炎的关节内骨样骨瘤:一例报告

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

作者信息

Fukuda Ryuichi, Matsuoka Masatake, Kawamura Daisuke, Endo Takeshi, Kanno-Okada Hiromi, Urita Atsushi, Matsui Yuichiro, Onodera Tomohiro, Iwasaki Norimasa

机构信息

Department of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.

Department of Orthopedic Surgery, Teine Keijinkai Hospital, Sapporo Teine Ku, Hokkaido, Japan.

出版信息

Ann Jt. 2022 Apr 15;7:20. doi: 10.21037/aoj-21-27. eCollection 2022.

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.

摘要

骨样骨瘤是良性的,通常为皮质内病变,最常累及长骨干骺端。存在夜间疼痛以及服用非甾体类抗炎药(NSAIDs)可缓解的特征性症状,这些有助于骨样骨瘤的诊断。我们报告一例18岁男性患者,其鹰嘴窝处患有骨样骨瘤,临床表现不典型。初始表现为类似关节炎的症状,如局部发热、活动时疼痛而非静息痛,以及活动范围受限。值得注意的是,NSAIDs对缓解其症状完全无效。磁共振成像显示肘关节周围骨髓水肿。症状对保守治疗无效,因此需要手术切除。组织病理学检查显示病变由相互吻合的编织骨和类骨组织组成。结合肿瘤大小小于2 cm,临床病理诊断为骨样骨瘤。术后疼痛立即缓解,术后2个月活动范围恢复。术后1年,患者未出现肿瘤复发或肘部疼痛加重,肘关节活动范围正常。对于青少年和青年患者的肘部关节炎进行鉴别诊断时应考虑骨样骨瘤,这是骨样骨瘤的发病高峰年龄。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11d5/10929422/0045c20be35d/aoj-07-20-f1.jpg

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