University of Calgary and Calgary Laboratory Services, Calgary, AB, Canada.
School of Medicine, Henry Ford Health System and Wayne State University, Detroit, MI, USA.
Histopathology. 2019 Aug;75(2):174-184. doi: 10.1111/his.13865. Epub 2019 Mar 21.
To describe a group of distinct low-grade oncocytic renal tumours that demonstrate CD117 negative/cytokeratin (CK) 7-positive immunoprofile.
We identified 28 such tumours from four large renal tumour archives. We performed immunohistochemistry for: CK7, CD117, PAX8, CD10, AMACR, e-cadherin, CK20, CA9, AE1/AE3, vimentin, BerEP4, MOC31, CK5/6, p63, HMB45, melan A, CD15 and FH. In 14 cases we performed array CGH, with a successful result in nine cases. Median patient age was 66 years (range 49-78 years) with a male-to-female ratio of 1:1.8. Median tumour size was 3 cm (range 1.1-13.5 cm). All were single tumours, solid and tan-brown, without a syndromic association. On microscopy, all cases showed solid and compact nested growth. There were frequent areas of oedematous stroma with loosely arranged cells. The tumour cells had oncocytic cytoplasm with uniformly round to oval nuclei, but without significant irregularities, and showed only focal perinuclear halos. Negative CD117 and positive CK7 reactivity were present in all cases (in two cases there was focal and very weak CD117 reactivity). Uniform reactivity was found for PAX8, AE1/AE3, e-cadherin, BerEP4 and MOC31. Negative stains included CA9, CK20, vimentin, CK5/6, p63, HMB45, Melan A and CD15. CD10 and AMACR were either negative or focally positive; FH was retained. On array CGH, there were frequent deletions at 19p13.3 (seven of nine), 1p36.33 (five of nine) and 19q13.11 (four of nine); disomic status was found in two of nine cases. On follow-up (mean 31.8 months, range 1-118), all patients were alive with no disease progression.
Low-grade oncocytic tumours that are CD117-negative/CK7-positive demonstrate consistent and readily recognisable morphology, immunoprofile and indolent behaviour.
描述一组具有独特形态学特征的低级别嗜酸细胞瘤,其免疫表型为 CD117 阴性/细胞角蛋白(CK)7 阳性。
我们从四个大型肾肿瘤档案中鉴定出 28 例此类肿瘤。我们进行了免疫组织化学检测:CK7、CD117、PAX8、CD10、AMACR、E-钙黏蛋白、CK20、CA9、AE1/AE3、波形蛋白、BerEP4、MOC31、CK5/6、p63、HMB45、黑色素 A、CD15 和 FH。在 14 例中进行了 array CGH 检测,其中 9 例获得了成功结果。中位患者年龄为 66 岁(范围 49-78 岁),男女比例为 1:1.8。中位肿瘤大小为 3cm(范围 1.1-13.5cm)。所有肿瘤均为单发、实性、棕褐色,无综合征相关性。镜下,所有病例均表现为实性、致密的巢状生长。常有水肿性基质区伴排列松散的细胞。肿瘤细胞具有嗜酸细胞细胞质,圆形至椭圆形核均匀一致,但无明显不规则性,仅见灶性核周晕。所有病例均表现为 CD117 阴性和 CK7 阳性(在 2 例中,CD117 存在局灶性和非常弱的反应性)。PAX8、AE1/AE3、E-钙黏蛋白、BerEP4 和 MOC31 表达均匀。CA9、CK20、波形蛋白、CK5/6、p63、HMB45、黑色素 A 和 CD15 染色阴性。CD10 和 AMACR 或阴性或局灶性阳性;FH 保留。array CGH 显示 19p13.3(9 例中的 7 例)、1p36.33(9 例中的 5 例)和 19q13.11(9 例中的 4 例)频繁缺失;2 例 9 例中存在二倍体状态。随访(平均 31.8 个月,范围 1-118),所有患者均存活,无疾病进展。
CD117 阴性/CK7 阳性的低级别嗜酸细胞瘤具有一致且易于识别的形态学、免疫表型和惰性行为。