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拇趾骨样骨瘤

Osteoid osteoma of the great toe.

作者信息

Hattori Hiroyuki, Takase Katsumi, Morohashi Akira

机构信息

Department of Orthopedic Surgery, Tokyo Medical University, Tokyo, Japan.

出版信息

Orthopedics. 2011 Aug 8;34(8):e432-5. doi: 10.3928/01477447-20110627-33.

Abstract

Osteoid osteoma is a relatively common osteoblastic lesion of benign skeletal neoplasms and occurs most commonly in the cortex of long bones, especially the femur and the tibia. Radiological characteristics are a nidus that appears as a small, relatively radiolucent zone within an area of extensive reactive sclerosis. Clinically, the lesion presents with increasing pain, is worse at night, and is relived by nonsteroidal anti-inflammatory drugs (NSAIDs). Osteoid osteomas involving the phalanges of the toes are uncommon, and its accurate preoperative diagnosis is difficult due to the unique clinical and radiological features. The features in the phalanx of the toe are soft tissue swelling and a nidus frequently located in the cancellous without osteosclerosis. This article presents a case of a 22-year-old man with osteoid osteoma in his distal phalanx of the hallux. A needle biopsy of his great toe revealed a small number of bacteria, so he was initially treated for osteomyelitis but with unsatisfactory results. The particular characteristics of clinical and imaging findings supported a diagnosis of osteoid osteoma in the distal phalanx of the hallux. After surgical removal of the tumor, his symptoms resolved. The pathological examination confirmed the suspected diagnosis. In a patient with chronic foot pain that changes to become nocturnal and disappears with NSAID administration, it is important to include osteoid osteoma as a differential diagnosis. A detailed assessment of both clinical and radiological features can lead to the correct diagnosis, which must be confirmed with histopathological examination to ensure adequate excision.

摘要

骨样骨瘤是一种相对常见的良性骨肿瘤性成骨病变,最常发生于长骨皮质,尤其是股骨和胫骨。放射学特征为瘤巢,表现为广泛反应性硬化区内的一个小的、相对透光的区域。临床上,该病变表现为疼痛逐渐加重,夜间更甚,非甾体类抗炎药(NSAIDs)可缓解。累及足趾趾骨的骨样骨瘤并不常见,由于其独特的临床和放射学特征,术前准确诊断较为困难。趾骨的特征为软组织肿胀,瘤巢常位于松质骨内且无骨质硬化。本文报道一例22岁男性,其拇趾远节趾骨患有骨样骨瘤。对其大脚趾进行穿刺活检发现少量细菌,因此最初按骨髓炎进行治疗,但效果不佳。临床和影像学表现的特殊特征支持拇趾远节趾骨骨样骨瘤的诊断。手术切除肿瘤后,其症状消失。病理检查证实了疑似诊断。对于慢性足部疼痛且转变为夜间疼痛并在服用NSAIDs后消失的患者,将骨样骨瘤纳入鉴别诊断很重要。对临床和放射学特征进行详细评估可得出正确诊断,必须通过组织病理学检查加以证实以确保充分切除。

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