A rare tumor at an unusual age: Pediatric bizarre parosteal osteochondromatous proliferation nora's lesion of the phalanx

IF 0.1 Q4 SURGERY Turkish Journal of Plastic Surgery Pub Date : 2022-04-01 DOI:10.4103/tjps.tjps_60_21
M. Çelik, Murat Kara, H. Unverdi, Uğur Koçer
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引用次数: 0

Abstract

Bizarre parosteal osteochondromatous proliferation (BPOP) is a rare lesion that usually arises in short bones of the hand and feet. It is typically seen in the third and fourth decades, seldom seen in the pediatric age group. A 6-year-old girl was presented with swelling over the ring finger of the left hand. The radiograph showed ectopic calcification and periosteal reaction in the ring finger. Computed tomography was performed, and a BPOP diagnosis was made on the preoperative finding. Excision of the lesion with overlying pseudocapsule and decortication was performed with a piezoelectric device. The patient is currently in a routine follow-up without recurrence. There is not enough data for treatment and follow-up BPOP in pediatric patients. The present case would contribute to the literature in the management of this rare presentation.
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一个罕见的肿瘤在一个不寻常的年龄:儿童奇异骨旁软骨瘤增生诺拉的损害的指骨
奇怪的骨旁软骨瘤增生(BPOP)是一种罕见的病变,通常发生在手和脚的短骨。它通常发生在第三和第四十年,很少见于儿科年龄组。一名六岁女孩左手无名指肿胀。x线片示无名指异位钙化及骨膜反应。进行计算机断层扫描,并根据术前发现进行BPOP诊断。用压电装置切除病变和覆盖的假包膜并去皮。患者目前正在进行常规随访,无复发。儿科患者的BPOP治疗和随访数据不足。本病例将有助于文献管理这一罕见的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
8
审稿时长
28 weeks
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