Orthopaedics, St John's Medical College Hospital, Bangalore, Karnataka, India
Orthopaedics, St John's Medical College Hospital, Bangalore, Karnataka, India.
BMJ Case Rep. 2024 Apr 2;17(4):e259712. doi: 10.1136/bcr-2024-259712.
Osteoid osteoma is a benign osteoblastic tumour with a predilection for the lower extremity that rarely affects the forearm. It is commonly seen in adolescents and young adults, and is seldom diagnosed in the paediatric age group. We report a boy in his early childhood who presented with a swelling over the distal forearm, which was incidentally noted by the mother 3 months ago. Plain radiographs showed diffuse sclerosis of the dorsal cortex of the distal radius. CT scan showed a central lucent nidus in the intramedullary region and surrounding sclerosis in the radial metaphysis, confirming the diagnosis of osteoid osteoma. The patient was successfully treated by surgical en bloc resection of the nidus and was asymptomatic at 1-year follow-up. Non-specific symptoms at presentation make it a challenge to diagnose osteoid osteoma in children and it needs to be considered in the differential diagnosis when radiographs show lytic lesions in the bone.
骨样骨瘤是一种良性成骨细胞瘤,好发于下肢,很少累及前臂。它常见于青少年和年轻成年人,很少在儿科年龄组中诊断。我们报告了一个幼儿病例,他的前臂远端出现肿胀,3 个月前母亲偶然发现。X 线平片显示桡骨远端背侧皮质弥漫性硬化。CT 扫描显示髓腔内中央透亮灶和桡骨干骺端周围硬化,确诊为骨样骨瘤。患者通过病灶整块切除术成功治疗,1 年随访时无症状。在儿童中,其表现为非特异性症状,诊断具有挑战性,当 X 线片显示骨内溶骨性病变时,需要考虑到该病的鉴别诊断。