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豌豆骨骨样骨瘤。它会出现在儿童身上吗?

Osteoid osteoma of the pisiform. Can it exist in a child?

作者信息

Papachristos Ioannis V, Pasparakis Dimitrios

机构信息

Second Orthopaedic Department of Children's Hospital of Athens 'Aglaia Kyriakou', Athens, Greece.

出版信息

J Pediatr Orthop B. 2014 Mar;23(2):172-5. doi: 10.1097/BPB.0000000000000012.

Abstract

Carpal osteoid osteomas are extremely rare, and only six cases in the pisiform have ever been described, but all concerned exclusively adults. We have treated a unique case of osteoid osteoma in the pisiform of a 13-year-old girl. We excised en bloc the nidus, which resulted in total excision of the pisiform. At follow-up after 15 years there was no recurrence and the patient remains asymptomatic with equal functionality of both hands. Henceforth, we must include osteoid osteoma in the differential diagnosis of pisiform lesions in children. En bloc resection prevents its recurrence and even the complete pisiform excision renders excellent results.

摘要

腕骨骨样骨瘤极为罕见,仅有6例关于豌豆骨骨样骨瘤的病例报道,且均为成人。我们治疗了1例13岁女孩豌豆骨骨样骨瘤的独特病例。我们完整切除了瘤巢,导致豌豆骨被完全切除。15年随访时无复发,患者双手功能相同且无症状。今后,我们必须将骨样骨瘤纳入儿童豌豆骨病变的鉴别诊断中。完整切除可防止其复发,甚至完全切除豌豆骨也能取得极佳效果。

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