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隐匿性和侵袭性:从结肠发生的具有横纹肌样特征的 /INI1 缺陷未分化癌:病例报告及全面文献复习。

Elusive and Aggressive: Unraveling /INI1-Deficient Undifferentiated Carcinoma With Rhabdoid Features Arising From the Colon: A Case Report and Comprehensive Literature Review.

机构信息

Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, USA.

出版信息

Int J Surg Pathol. 2024 Dec;32(8):1582-1587. doi: 10.1177/10668969241232699. Epub 2024 Feb 20.

Abstract

Undifferentiated carcinomas are highly aggressive tumors with a dismal prognosis. A subset of these tumors has been associated with inactivation or mutations of the Switch/Sucrose Nonfermenting (SWI/SNF) remodeling complex. Our understanding of the relationship between the clinicopathological features and molecular profiling of SWI/SNF-deficient undifferentiated carcinoma is still evolving due to its rarity. We herein present a rare tumor of undifferentiated carcinoma with INI1 deficiency arising from the colon. The histology revealed a tumor composed of sheets of discohesive, high-grade epithelioid cells with rhabdoid morphology along with anaplastic giant cells. Additionally, there was a significant infiltration of inflammatory cells in the background. Immunohistochemical (IHC) analysis supported the diagnosis of carcinoma with loss of INI1 expression, the tumor was mismatch repair protein proficient. Molecular analysis demonstrated an oncogenic (p.G12D), whereas it was wild-type , and wild-type . The diagnosis of SWI/SNF-deficient undifferentiated carcinoma can be challenging. Correlation with clinical findings, in conjunction with IHC work-up and molecular analysis, is of utmost importance to arrive at the appropriate diagnosis and exclude potential mimics.

摘要

未分化癌是一种侵袭性高、预后极差的肿瘤。这些肿瘤中有一部分与 Switch/Sucrose Nonfermenting(SWI/SNF)重塑复合物的失活或突变有关。由于其罕见性,我们对 SWI/SNF 缺陷型未分化癌的临床病理特征与分子谱之间的关系的认识仍在不断发展。本文报道了一例罕见的结肠起源的 INI1 缺陷型未分化癌。组织学显示肿瘤由片状离散的高级上皮样细胞组成,具有横纹肌样形态,同时伴有间变巨细胞。此外,背景中还有大量炎症细胞浸润。免疫组织化学(IHC)分析支持该肿瘤为具有 INI1 表达缺失的癌,该肿瘤错配修复蛋白功能正常。分子分析显示存在致癌性突变(p.G12D),而 和 则为野生型。SWI/SNF 缺陷型未分化癌的诊断具有挑战性。与临床发现相关联,结合 IHC 检查和分子分析,对于得出正确的诊断并排除潜在的类似物非常重要。

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