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乳腺CD34缺陷型肌纤维母细胞瘤的特征描述。

Characterization of CD34-deficient myofibroblastomas of the breast.

作者信息

D'Alfonso Timothy M, Subramaniyam Shivakumar, Ginter Paula S, Mosquera Juan Miguel, Croyle Jaclyn, Liu Yi-Fang, Rubin Mark A, Shin Sandra J

机构信息

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.

Institute for Precision Medicine of Weill Cornell and New York-Presbyterian Hospital, New York, NY, USA.

出版信息

Breast J. 2018 Jan;24(1):55-61. doi: 10.1111/tbj.12835. Epub 2017 May 30.

Abstract

Mammary myofibroblastoma is a benign spindle cell tumor that can show variable morphologic patterns and lines of differentiation. Diffuse and strong immunohistochemical expression of CD34 is a characteristic of myofibroblastoma and greatly aids in confirming a diagnosis. Myofibroblastoma has been shown to belong to a family of CD34-positive tumors with similar morphology that show a deletion of 13q14, which includes RB1 and FOXO1A genes. The purpose of this study was to better understand a subset of myofibroblastomas that is characteristically CD34-deficient by immunohistochemistry. Six myofibroblastomas were studied by immunohistochemistry and fluorescence in situ hybridization (FISH) for RB1. Patients included five women and one man, aged 41-85 years (median, 52.5). Tumor size ranged from 0.4 to 1.5 cm (mean, 0.95). Tumors showed spindle cell morphology in five cases and epithelioid features in one case. Two tumors showed complete lack of CD34 staining. The remaining showed weak focal or weak patchy CD34 staining. Dichotomous staining was seen in one case with CD34-positive spindle cell areas and CD34-negative myxoid areas. All six tumors showed ER expression, five of six showed desmin expression, and four of six showed bcl-2 positivity. Two of six (33.3%) tumors showed deletion of RB1 by FISH, including one that showed loss of Rb immunohistochemical staining. Myofibroblastomas uncommonly show absent/focal expression of CD34, a potential diagnostic pitfall, particularly in small samples. Characteristic staining with other immunohistochemical markers is seen which can aid in confirming the diagnosis. These tumors may harbor deletion of RB1, similar to CD34-positive myofibroblastomas, and this deletion may not correlate with loss of Rb by immunohistochemistry.

摘要

乳腺肌纤维母细胞瘤是一种良性梭形细胞肿瘤,可呈现多种形态学模式和分化谱系。CD34弥漫性和强免疫组化表达是肌纤维母细胞瘤的特征,对确诊有很大帮助。肌纤维母细胞瘤已被证明属于一类形态相似的CD34阳性肿瘤家族,这些肿瘤显示13q14缺失,其中包括RB1和FOXO1A基因。本研究的目的是更好地了解免疫组化特征性CD34缺失的一部分肌纤维母细胞瘤。通过免疫组化和RB1荧光原位杂交(FISH)研究了6例肌纤维母细胞瘤。患者包括5名女性和1名男性,年龄41 - 85岁(中位年龄52.5岁)。肿瘤大小为0.4至1.5 cm(平均0.95 cm)。5例肿瘤表现为梭形细胞形态,1例表现为上皮样特征。2例肿瘤CD34染色完全缺失。其余肿瘤表现为弱局灶性或弱片状CD34染色。1例可见二分染色,有CD34阳性梭形细胞区域和CD34阴性黏液样区域。所有6例肿瘤均显示ER表达,6例中有5例显示结蛋白表达,6例中有4例显示bcl-2阳性。6例中有2例(33.3%)肿瘤通过FISH显示RB1缺失,其中1例显示Rb免疫组化染色缺失。肌纤维母细胞瘤很少表现出CD34缺失/局灶性表达,这是一个潜在的诊断陷阱,尤其是在小样本中。可见其他免疫组化标志物的特征性染色,有助于确诊。这些肿瘤可能存在RB1缺失,类似于CD34阳性肌纤维母细胞瘤,且这种缺失可能与免疫组化检测的Rb缺失不相关。

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