首次描述原发性 SMARCA4 缺失的唾液腺癌

David Oestreicher , Irina Kostyuchek , Philipp Ströbel , Dirk Beutner , Tobias Dombrowski
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引用次数: 0

摘要

在肺部、胸部、食道和卵巢等多个器官中发现了 SMARCA4 缺失的肿瘤。在某些情况下,SMARCA4 缺失肿瘤与特定的组织学亚型有关,如卵巢小细胞癌、高钙血症型(SCCOHT)。这些肿瘤通常是高级别和侵袭性肿瘤,具有早期转移和预后不良的倾向。SMARCA4(又称 BRG1)是一种染色质重塑蛋白,在基因表达调控中发挥着重要作用。SMARCA4缺失会导致细胞周期调节因子和DNA损伤应答基因的表达改变,从而导致基因组不稳定和肿瘤发生。我们描述了第一例唾液腺 SMARCA4 缺失型癌的临床病例,该病例是在快速生长的腮腺病变中发现的。最初,肿瘤有同侧颈淋巴结转移,但无任何远处转移。肿瘤手术进行了腮腺全切除术和左侧颈部清扫术,之后进行了辅助放疗。放疗结束后不久,CT扫描再次分期显示多处转移。随后开始使用 PDL1 抑制剂进行免疫治疗,并对骨转移灶进行了额外的姑息性放疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First description of a primary SMARCA4-deficient carcinoma of the salivary glands

SMARCA4-deficient neoplasms have been identified in several organs, including the lung, thorax, esophagus and ovary. In some cases, SMARCA4-deficient neoplasms are associated with specific histologic subtypes, such as small cell carcinoma of the ovary, hypercalcemic type (SCCOHT). These tumors are often high-grade and aggressive, with a propensity for early metastasis and poor prognosis. SMARCA4 (also known as BRG1) is a chromatin-remodeling protein that plays an important role in gene expression regulation. SMARCA4 loss results in altered expression of cell cycle regulators and DNA damage response genes, leading to genomic instability and oncogenesis. We describe the first clinical case of a SMARCA4-deficient carcinoma of the salivary glands, found in a rapidly growing parotid lesion. Initially, the tumor had ipsilateral cervical lymph node metastases without any distant metastases. After tumor surgery with total parotidectomy and neck dissection on the left side, adjuvant radiotherapy was performed. Shortly after completion of radiotherapy, re-staging by a CT scan showed metastases at multiple sites. Immunotherapy with a PDL1 inhibitor and additional palliative radiotherapy for the bony metastases was then initiated.

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