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泌尿生殖道和妇科肿瘤中的GLI1基因改变

GLI1 Gene Alterations in Neoplasms of the Genitourinary and Gynecologic Tract.

作者信息

Argani Pedram, Boyraz Baris, Oliva Esther, Matoso Andres, Gross John, Fridman Eddie, Zhang Lei, Dickson Brendan C, Antonescu Cristina R

机构信息

Departments of Pathology.

Oncology.

出版信息

Am J Surg Pathol. 2022 May 1;46(5):677-687. doi: 10.1097/PAS.0000000000001844.

Abstract

We report 4 neoplasms of the kidney (2 cases) and uterus (2 cases) harboring rearrangements or amplifications of the GLI1 gene, which because of their unusual clinical presentation, morphology, and immunoprofile mimicked other neoplasms, causing significant diagnostic challenge. The neoplasms occurred in 4 female patients ages 33 to 88 years. Histologically they all demonstrated nodular growth, solid architecture, bland epithelioid to ovoid-spindle cells with pale cytoplasm set in a variably myxoid or hyalinized stroma. One uterine tumor also demonstrated a focal round cell pattern, while another demonstrated focal pleomorphism. Unlike most previously reported neoplasms with these genetic abnormalities, the neoplasms in the current series were negative for S100 protein and minimally reactive for actin. All labeled for CD10 and cyclin D1, while 2 labeled for estrogen receptor and BCOR and 1 labeled for desmin, raising consideration of endometrial stromal sarcoma, myxoid leiomyosarcoma, metastatic breast carcinoma, and glomus tumor. One renal neoplasm demonstrated a GLI1-FOXO4 gene fusion and the other harbored a GLI1 gene rearrangement (unknown partner). The 2 uterine neoplasms exhibited GLI1 gene amplifications. GLI1-altered neoplasms (particularly those with GLI1 amplification) show variable morphology and lack a consistent immunophenotype, and thus may trigger diagnostic challenges which can be resolved by molecular testing.

摘要

我们报告了4例分别发生于肾脏(2例)和子宫(2例)的肿瘤,这些肿瘤存在GLI1基因重排或扩增。由于其不寻常的临床表现、形态学和免疫表型,它们酷似其他肿瘤,给诊断带来了巨大挑战。这些肿瘤发生于4名年龄在33至88岁的女性患者。组织学上,它们均表现为结节状生长、实性结构,由温和的上皮样至卵圆形梭形细胞组成,胞质淡染,位于不同程度黏液样或玻璃样变的间质中。1例子宫肿瘤还表现为局灶性圆形细胞模式,另1例表现为局灶性多形性。与大多数先前报道的具有这些基因异常的肿瘤不同,本系列中的肿瘤S100蛋白阴性,肌动蛋白反应性最低。所有肿瘤均表达CD10和细胞周期蛋白D1,2例表达雌激素受体和BCOR,1例表达结蛋白,这使得考虑诊断为子宫内膜间质肉瘤、黏液样平滑肌肉瘤、转移性乳腺癌和血管球瘤。1例肾肿瘤显示GLI1-FOXO4基因融合,另1例存在GLI1基因重排(未知配对基因)。2例子宫肿瘤表现为GLI1基因扩增。GLI1改变的肿瘤(尤其是那些具有GLI1扩增的肿瘤)形态多样,缺乏一致的免疫表型,因此可能引发诊断挑战,而通过分子检测可以解决这些挑战。

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