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ALK是子宫炎症性肌纤维母细胞肿瘤特异性诊断标志物

时间:2019-09-27 17:01:01  阅读:9244+ 作者:91360智慧病理网

原标题:ALK是子宫炎症性肌纤维母细胞肿瘤特异性确诊标志物

  • 来历:The American Journal of Surgical Pathology中文版

--本文经《美国外科病理学杂志》授权发布,其他媒体转载或引证须经《美国外科病理学杂志》赞同,不然追查法律责任。

摘要:炎症性肌纤维母细胞肿瘤(inflammatory myofibroblastictumor, IMT)是一种具有中度恶性潜能的肌纤维母细胞/纤维母细胞肿瘤,一般特征性地表现为ALK与多种伴侣基因发作基因交融,导致激酶抑制剂靶向的ALK信号通路激活。IMT可发作在女人生殖道,子宫(宫体和宫颈)是最常见的部位。近期研讨标明,发作于女人生殖道的IMT尚未被充分认识,主张至少要进行ALK免疫组织化学染色。本研讨的意图是评价ALK免疫组织化学染色对从子宫间叶和混合性上皮/间叶肿瘤中识别出IMT的特异性。咱们对14例经分子检测证明的子宫IMT和260例其他类型子宫单纯性间叶和混合性上皮/间叶肿瘤进行ALK免疫组织化学染色。肿瘤细胞呈细胞质和/或细胞膜上色的病例均被认为是ALK阳性。一切14例IMT经RNA测序均被证明具有ALK基因交融,且14例病例的ALK染色均出现核旁加剧的颗粒状细胞质上色形式。一切其他单纯性间叶肿瘤和混合性上皮/间叶肿瘤的ALK均为阴性(彻底缺少上色)。咱们的结果标明,ALK是具有ALK交融的子宫间叶肿瘤的一种高度特异的免疫组化符号物。在子宫间叶肿瘤(尤其是呈黏液样间质改动的平滑肌肿瘤)的确诊中,假如观察到ALK阳性,高度考虑确诊为IMT。

关键词:ALK, 子宫肉瘤,炎症性肌纤维母细胞肿瘤,基因交融

Am J Surg Pathol 2018;42:1353-1359)

美国外科病理学杂志中文版2019年第2期全文No.1

(杨 丽 翻译 张 静 审校)

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©2018 Wolters Kluwer Health

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