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一部分胸段SMARCA4缺陷型未分化肿瘤表达GATA3。

A Subset of Thoracic SMARCA4-Deficient Undifferentiated Tumors Express GATA3.

作者信息

Coconubo Daniel Martinez, Wangsiricharoen Sintawat, Pettus Jason R, Linos Konstantinos, Pinto Andre, Wang Wei-Lien, Kerr Darcy A, Cloutier Jeffrey M

机构信息

Department of Pathology and Laboratory Medicine, Dartmouth-Hitchcock Medical Center, One Medical Center Drive, Lebanon, NH, USA.

Geisel School of Medicine at Dartmouth, Hanover, NH, USA.

出版信息

Int J Surg Pathol. 2024 Jun;32(4):684-691. doi: 10.1177/10668969231188904. Epub 2023 Jul 17.

Abstract

Thoracic SMARCA4-deficient undifferentiated tumor (SMARCA4-UT) is a rare and highly aggressive malignant neoplasm characterized by high-grade undifferentiated morphologic features and recurrent inactivating mutations of . These tumors consistently exhibit loss of SMARCA4 (BRG1) while displaying variable expression of other nonspecific markers. Recently, we encountered a SMARCA4-UT demonstrating immunoreactivity for GATA3, and we sought to characterize this phenomenon in a larger series. A total of nine SMARCA4-UTs were examined from 3 large academic institutions. The clinicopathologic and molecular characteristics were studied and GATA3 immunohistochemistry was performed. The cohort included 5 male and 4 female patients, with a median age of 54 years and a median smoking history of 37 pack-years. At initial diagnosis, mediastinal lymph node involvement was observed in 5 patients (56%) while distant metastases were present in 7 patients (78%). The median survival was 6 months. Histologically, the tumors were characterized by sheets of undifferentiated epithelioid and/or rhabdoid cells, accompanied by frequent mitotic figures and necrosis. Immunohistochemically, all tumors displayed a complete loss of BRG1 expression. Notably, 4 of 9 tumors (44%) were positive for GATA3 expression, including one tumor that exhibited strong and diffuse immunoreactivity. GATA3 expression in SMARCA4-UT may pose diagnostic challenges, requiring differentiation from other GATA3-positive tumors. This distinction is crucial for accurate prognostication and treatment decisions.

摘要

胸段SMARCA4缺陷型未分化肿瘤(SMARCA4-UT)是一种罕见且高度侵袭性的恶性肿瘤,其特征为高级别未分化形态学特征以及[相关基因]的复发性失活突变。这些肿瘤始终表现出SMARCA4(BRG1)缺失,同时其他非特异性标志物表达各异。最近,我们遇到一例对GATA3呈免疫反应性的SMARCA4-UT,我们试图在更大系列中对这一现象进行特征描述。从3家大型学术机构共检测了9例SMARCA4-UT。研究了其临床病理和分子特征,并进行了GATA3免疫组化检测。该队列包括5例男性和4例女性患者,中位年龄54岁,中位吸烟史37包年。初诊时,5例患者(56%)观察到纵隔淋巴结受累,7例患者(78%)存在远处转移。中位生存期为6个月。组织学上,肿瘤的特征是成片的未分化上皮样和/或横纹肌样细胞,伴有频繁的有丝分裂象和坏死。免疫组化方面,所有肿瘤均显示BRG1表达完全缺失。值得注意的是,9例肿瘤中有4例(44%)GATA3表达呈阳性,其中1例肿瘤表现出强而弥漫的免疫反应性。SMARCA4-UT中GATA3表达可能带来诊断挑战,需要与其他GATA3阳性肿瘤相鉴别。这种鉴别对于准确的预后评估和治疗决策至关重要。

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