下颌骨远端切除性骨肉瘤,特别强调免疫组化和分子特征:病例报告及文献综述

Q3 Dentistry Oral Surgery Pub Date : 2023-11-20 DOI:10.1111/ors.12860
Eram Khan, Saloni Verma, N. Sivakumar, Pooja Sharma, Shaleen Chandra, Shalini Gupta
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引用次数: 0

摘要

扩张性骨肉瘤(TOS)是一种不常见的病变,约占所有骨肉瘤的 0.4%-12%,好发于年轻人。它最常见于长骨干骺端,表现为疼痛的溶骨性肿块,组织病理学特征为恶性成骨细胞内衬的扩张、充血的血管间隙和类骨形成。它与动脉瘤性骨囊肿和骨巨细胞瘤等良性病变的临床、放射学和病理学特征具有可交换性。报告一例 17 岁女性患者的颌骨毛细血管扩张性骨肉瘤病例,特别强调分子诊断和治疗模块。免疫组化结果显示,肿瘤细胞的 SATB2 呈强阳性,CDK4、MDM2、panCK、CD31、desmin、NKX2.2 和 TLE1 呈阴性。CDK4和MDM2基因的荧光原位杂交也呈阴性。考虑到其在颌骨中的罕见性以及与其他良性病变的临床病理重叠性,该实体的诊断对治疗计划和预后意义至关重要。此外,迄今为止,仅有五例颅面部 TOS 病例被报道。在此,我们报告了第六例此类病例,并详细说明了其免疫组化和分子方面的情况。
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Telengiectatic osteosarcoma of mandible with special emphasis on immunohistochemical and molecular characteristics: A case report with review of literature
Telangiectatic osteosarcoma (TOS) is an uncommon pathology accounting for about 0.4%–12% of all osteosarcomas with predilection for younger adults. It is most frequently seen in the metaphysis of long bones, appearing as painful osteolytic mass that histopathologically characterized by dilated, blood‐filled vascular spaces lined by malignant osteoblasts along with osteoid formation. It has exchangeable clinical, radiological and pathological features with benign lesions like aneurysmal bone cyst and giant cell tumour of bone as well. Thus, delineating this malignancy from its benign counterparts is a crucial part in the therapeutic management.To report a case of telengiectatic osteosarcoma of jaw in a 17 year old female patient with special highlights on molecular diagnostics and therapeutic modules.A panel of immunohistochemical markers comprising of SATB2, CDK4, MDM2, panCK, CD31, desmin, NKX2.2 and TLE1 were employed in combination with fluorescent in‐situ hybridization to detect the prevalence of rearrangement in CDK4 and MDM2 genes.On immunohistochemistry, the neoplastic cells were strongly positive for SATB2 and negative for CDK4, MDM2, panCK, CD31, desmin, NKX2.2 and TLE1. Fluorescent in‐situ hybridization of CDK4 and MDM2 genes was also negative.Considering its rarity in jaws combined with clinicopathological overlap with other benign pathologies, diagnosis of this entity is crucial in treatment planning and prognostic significance. Moreover, only five cases of TOS have been reported so far in the craniofacial region. Here, we have reported the sixth case of its kind with detailed clarification pertaining to its immunohistochemical and molecular aspects.
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来源期刊
Oral Surgery
Oral Surgery Medicine-Surgery
CiteScore
0.90
自引率
0.00%
发文量
80
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