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罕见下颌转移性富巨细胞骨肉瘤病例:更新及鉴别诊断要点。

A rare case of a metastatic giant cell-rich osteosarcoma of the mandible: Update and differential diagnostic considerations.

机构信息

Department of Dentistry, School of Dentistry, Universidade Federal de Sergipe, Aracaju, SE, Brazil.

Postgraduate Program in Oral Pathology, School of Dentistry, Universidade Federal do Rio Grande do Norte, Natal, RN, Brazil.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol. 2021 May;131(5):e163-e169. doi: 10.1016/j.oooo.2020.10.009. Epub 2020 Oct 17.

DOI:10.1016/j.oooo.2020.10.009
PMID:33187945
Abstract

A metastatic giant cell-rich osteosarcoma (GCRO) to the jaws is an exceedingly rare neoplasm. To date, fewer than 10 cases have been reported in the English language literature. In this article, we describe an additional case of a metastatic GCRO that presented the diagnostic challenge of a painless mass in the posterior mandible of a 19-year-old girl who exhibited rapid and aggressive local growth. The lesion was confirmed radiologically as an ill-defined expansive osteolytic mass showing cortical perforation. Microscopically, the presence of osteoclast-like giant cells permeated with atypical oval and rounded mesenchymal cells in a fibrovascular stroma, cellular atypia, and scarce osteoid formation were observed. Immunohistochemistry revealed the Ki-67 proliferative index in 50% of positive cells, positivity for vimentin and CD68, as well as scarce positivity for CDK4. The patient's medical history involved a GCRO in the proximal ulna. This report highlights the aggressive behavior of GCRO and its high capacity for metastasis to different parts of the body. Clinicians, pathologists, and surgeons should be aware of the giant cell-rich variant of osteosarcoma of the jaws, an imminent "wolf in a sheep's skin", because its indolent but unrelenting growth and dissemination, with radiographic and histologic characteristics that may represent a diagnostic pitfall regarding aggressive central giant cell lesions of the jaws.

摘要

发生于颌骨的转移性巨细胞丰富型骨肉瘤(GCRO)是一种极为罕见的肿瘤。迄今为止,在英语文献中报道的病例少于 10 例。本文描述了另外一例转移性 GCRO 病例,该病例具有以下诊断挑战:19 岁女孩的下颌后无痛性肿块,表现为快速且侵袭性的局部生长。该病变在影像学上被确认为界限不清的扩张性溶骨性肿块,伴有皮质穿孔。显微镜下,可见破骨样巨细胞存在,伴有不典型的椭圆形和圆形间叶细胞弥漫于纤维血管基质中,存在细胞异型性和稀少的骨样组织形成。免疫组织化学显示 Ki-67 增殖指数为 50%的阳性细胞,波形蛋白和 CD68 阳性,以及 CDK4 弱阳性。患者的病史涉及近端尺骨的 GCRO。本报告强调了 GCRO 的侵袭性行为及其向身体不同部位转移的高能力。临床医生、病理学家和外科医生应该意识到颌骨富含巨细胞的骨肉瘤变体,这是一种迫在眉睫的“披着羊皮的狼”,因为它具有惰性但持续不断的生长和扩散,其影像学和组织学特征可能代表颌骨侵袭性中央巨细胞瘤病变的诊断陷阱。

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