首页> 美国卫生研究院文献>Head and Neck Pathology >Bizarre Parosteal Osteochondromatous Proliferation (Nora’s Lesion) of the Mandible. A Rare Bony Lesion
【2h】

Bizarre Parosteal Osteochondromatous Proliferation (Nora’s Lesion) of the Mandible. A Rare Bony Lesion

机译:下颌骨怪异的骨旁骨软骨瘤增生(诺拉病变)。罕见的骨病

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Bizarre parosteal osteochondromatous proliferation (BPOP) also eponymically called “Nora’s lesion”, is a rare benign reactive bone lesion first reported in 1983. BPOP occurs classically on the bones of the hands and feet and long bones. This lesion can easily be confused, both clinically and microscopically, with other benign and malignant lesions of bone, including osteochondroma, parosteal osteosarcoma, myositis ossificans and reactive periostitis. BPOP has been reported to have a high rate of recurrence. Only 3 cases of BPOP of the head and neck have been reported in the literature, of which one involved the maxilla. We present a rare case of BPOP involving the mandible in a 10 year old African American male. Microscopically, a fibro-cartilaginous cap giving rise to a proliferation of variably mineralized osteophytic finger-like projections of bone was seen. Multiple trabeculae of “blue bone” were noted as well as numerous atypical appearing chondrocytes. The lesion recurred within 4 months following the initial excision but has not recurred to date after the second local excision. To the best of our knowledge, this is the first report of BPOP arising in the mandible. In addition, we discuss the clinical and microscopic features, differential diagnosis, and prognosis of this rare entity. We present a case of BPOP of the mandible and believe this is the first report of such a case in the mandible.
机译:怪异的骨旁骨软骨瘤增生(BPOP),又名“诺拉氏病变”,是一种罕见的良性反应性骨病变,于1983年首次报道。BPOP通常发生在手,脚和长骨的骨骼上。在临床上和显微镜下,该病变很容易与其他骨的良性和恶性病变混淆,包括骨软骨瘤,骨旁骨肉瘤,骨化性肌炎和反应性骨膜炎。据报道,BPOP具有较高的复发率。文献中仅报道了3例头颈部BPOP病例,其中1例涉及上颌骨。我们介绍了罕见的BPOP病例,涉及一名10岁的非洲裔美国男性的下颌骨。在显微镜下,可以看到一个纤维状的软骨帽,使骨骼的矿化的骨赘手指状突起变矿化。注意到“蓝骨”的多个小梁以及许多非典型出现的软骨细胞。病变在初次切除后的4个月内复发,但直到第二次局部切除后才复发。据我们所知,这是下颌骨中BPOP的首次报道。此外,我们讨论了这种罕见实体的临床和微观特征,鉴别诊断和预后。我们介绍了下颌骨的BPOP病例,并认为这是该病例在下颌骨中的首次报道。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号