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下颌骨奇异型骨旁骨软骨瘤样增生(诺拉病变),一种罕见的骨病变。

Bizarre parosteal osteochondromatous proliferation (Nora's Lesion) of the mandible. a rare bony lesion.

作者信息

Dashti H M, Reith J D, Schlott B J, Lewis E L, Cohen D M, Bhattacharyya I

机构信息

Department of Oral & Maxillofacial Diagnostic Sciences, University of Florida College of Dentistry, 1600 Archer Road, P.O. Box: 100414, Gainesville, FL 32610, USA.

出版信息

Head Neck Pathol. 2012 Jun;6(2):264-9. doi: 10.1007/s12105-011-0311-x. Epub 2011 Nov 18.

Abstract

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.

摘要

怪异的骨旁骨软骨瘤样增生(BPOP),也被称为“诺拉病变”,是一种罕见的良性反应性骨病变,于1983年首次报道。BPOP典型地发生在手、足和长骨的骨骼上。这种病变在临床和显微镜下都很容易与其他骨的良性和恶性病变相混淆,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的复发率很高。文献中仅报道了3例头颈部BPOP,其中1例累及上颌骨。我们报告1例罕见的BPOP累及一名10岁非裔美国男性的下颌骨。显微镜下可见一个纤维软骨帽,其产生了不同程度矿化的骨赘指状突起的增生。观察到多个“蓝色骨”小梁以及许多形态不典型的软骨细胞。病变在初次切除后4个月内复发,但在第二次局部切除后至今未复发。据我们所知,这是下颌骨发生BPOP的首例报告。此外,我们讨论了这种罕见实体的临床和显微镜特征、鉴别诊断及预后。我们报告了1例下颌骨BPOP病例,并认为这是下颌骨此类病例的首例报告。

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