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不常见的牙源性癌类似物:颞下颌关节原发性滑膜肉瘤——分子诊断的关键作用。

Unusual mimicker of odontogenic carcinoma: Primary synovial sarcoma of the temporomandibular joint- a critical role for molecular diagnosis.

机构信息

Anatomic Pathology, Head and Neck Disease Alignment Team, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.

Department of Thoracic and Head and Neck Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.

出版信息

Pathol Res Pract. 2022 Apr;232:153824. doi: 10.1016/j.prp.2022.153824. Epub 2022 Feb 25.

Abstract

BACKGROUND

Synovial sarcomas (SS) are malignant tumors originating from pluripotent mesenchymal cells, with predilection for periarticular areas, as deep-seated soft tissue tumors. Treatment of SS of the head and neck (HN) is usually radical local excision and additional radiation or (neo)adjuvant chemotherapy or both. SS are characterized by a specific SS18-SSX1/2/4 fusion gene. SS have several morphological variants: monophasic, biphasic, or poorly differentiated.

METHODS AND RESULTS

We describe a SS of mandibular condyle that showed an overwhelming (>95%) epithelial cell component mimicking odontogenic carcinoma. One year prior to presentation, a woman developed a 2.5 cm destructive bone lesion in the left mandibular condyle. The initial diagnosis of ameloblastoma on biopsy was changed to odontogenic carcinoma on the surgical specimen. Four months later a computed tomography (CT) revealed local recurrence; another month later, magnetic resonance imaging (MRI) depicted a new left temporal lobe brain lesion. The patient started on a carboplatin and paclitaxel therapy, with no clinical or radiologic benefit. Subsequently she was presented for another opinion. The pathology material was re-reviewed. Fluorescence in situ hybridization (FISH) resulted a positive result for SS18 (SYT) rearrangement; next generation sequencing (NGS sarcoma fusion panel) reported an SS18-SSX2 fusion transcript. Based on molecular testing the tumor was reclassified as synovial sarcoma. Her systemic treatment was changed to anthracycline based systemic therapy.

CONCLUSIONS

This case emphasizes the importance of molecular approaches in diagnostic pathology. Accurate diagnosis is imperative to avoid misclassification as carcinoma (metastasis or primary e.g., odontogenic carcinoma), carcinosarcoma or a different sarcoma type with epithelioid or epithelial differentiation and to determine proper treatment.

摘要

背景

滑膜肉瘤(SS)是一种起源于多能间充质细胞的恶性肿瘤,好发于关节周围区域,属于深部软组织肿瘤。头颈部(HN)SS 的治疗通常为根治性局部切除,附加放疗或(新)辅助化疗,或两者兼用。SS 的特征在于存在特异性的 SS18-SSX1/2/4 融合基因。SS 有几种形态学变异型:单相型、双相型或低分化型。

方法和结果

我们描述了一例下颌骨髁突 SS,其上皮细胞成分占压倒性优势(>95%),类似于牙源性癌。在出现症状前 1 年,一名女性在左侧下颌骨髁突处出现了一个 2.5cm 的破坏性骨病变。活检的最初诊断为造釉细胞瘤,手术标本的诊断更改为牙源性癌。4 个月后 CT 显示局部复发;1 个月后 MRI 显示左侧颞叶有新的脑部病变。患者开始接受卡铂和紫杉醇治疗,但无临床或影像学获益。随后她来就诊寻求其他意见。重新审查了病理材料。荧光原位杂交(FISH)结果显示 SS18(SYT)重排阳性;下一代测序(NGS 肉瘤融合面板)报告存在 SS18-SSX2 融合转录本。根据分子检测,肿瘤重新分类为滑膜肉瘤。她的全身治疗改为基于蒽环类的全身治疗。

结论

本例强调了分子方法在诊断病理学中的重要性。准确诊断对于避免误诊为癌(转移或原发性,例如牙源性癌)、癌肉瘤或具有上皮样或上皮分化的不同肉瘤类型至关重要,并且有助于确定适当的治疗方法。

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