Pathology Service, WRN219, Massachusetts General Hospital, Boston, MA 02114; Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
Pathology Service, WRN219, Massachusetts General Hospital, Boston, MA 02114; Department of Pathology, Harvard Medical School, Boston, MA 02115, USA; Department of Otolaryngology, Massachusetts Eye and Ear, Boston, MA 02114, USA.
Hum Pathol. 2018 Dec;82:32-38. doi: 10.1016/j.humpath.2018.06.033. Epub 2018 Jul 3.
The non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) and encapsulated follicular variant of papillary thyroid carcinoma (EFVPTC) are distinguished from classical papillary thyroid carcinoma with predominantly follicular architecture (CPTCPFA) by distinct histomorphologic and molecular features. CPTCPFA frequently harbor the oncogenic variant BRAFV600E while NIFTP and EFVPTC are largely RAS driven. CPTCPFA have rare papillae and intranuclear pseudoinclusions that may distinguish them from NIFTP or EFVPTC. We evaluated for BRAFV600E mutation using mutation-specific BRAF (VE1) antibody immunohistochemistry (BRAFVE) as part of an immunomorphologic tumor panel, often including HBME1, for follicular-patterned lesions with nuclear atypia. An archival search identified cases of NIFTP, CPTCPFA, or EFVPTC between 2015-2017, and demographic data, tumor characteristics, molecular data, and metastases were documented. Our search yielded 275 tumors across categories, and 208 were tested with BRAFVE. Sixty-one NIFTP and 31 sub-centimeter NIFTP were tested, and none (0/92) were positive for BRAFVE. Nineteen CPTCPFA and 14 sub-centimeter CPTCPFA were tested with 18 of 33 (54.5%) BRAFVE positive. Sixty-one EFVPTC and 21 sub-centimeter EFVPTC were tested, with 12 of 81 (14.8%) positive. Mean follow-up time was 1.5 years. Six (4.6%) patients with concurrent classical papillary thyroid carcinoma had local lymph node metastases at time of NIFTP diagnosis, as did 15 of 111 (13.5%) EFVPTC. Six of 34 (14.7%) CPTCPFA had local nodal metastases with five being considered the primary lesion. One EFVPTC (0.9%), BRAFVE negative, metastasized to femur. The findings indicate that BRAFVE used in conjunction with routine sampling of follicular-patterned tumors is a useful diagnostic adjuvant.
具有滤泡样核特征的非侵袭性滤泡甲状腺肿瘤(NIFTP)和包膜滤泡型甲状腺乳头状癌(EFVPTC)与主要呈滤泡结构的经典甲状腺乳头状癌(CPTCPFA)通过明显的组织形态学和分子特征区分开来。CPTCPFA 常含有致癌变体 BRAFV600E,而 NIFTP 和 EFVPTC 主要由 RAS 驱动。CPTCPFA 有罕见的乳头和核内假包涵体,这可能使它们与 NIFTP 或 EFVPTC 区分开来。我们使用突变特异性 BRAF (VE1) 抗体免疫组化(BRAFVE)评估 BRAFV600E 突变,作为免疫形态肿瘤组的一部分,通常包括 HBME1,用于具有核异型性的滤泡模式病变。存档搜索确定了 2015-2017 年之间的 NIFTP、CPTCPFA 或 EFVPTC 病例,并记录了人口统计学数据、肿瘤特征、分子数据和转移情况。我们的搜索产生了 275 个分类肿瘤,其中 208 个进行了 BRAFVE 检测。61 个 NIFTP 和 31 个亚厘米 NIFTP 进行了检测,92 个均为阴性(0/92)。19 个 CPTCPFA 和 14 个亚厘米 CPTCPFA 进行了检测,其中 33 个中的 18 个(54.5%)为阳性。61 个 EFVPTC 和 21 个亚厘米 EFVPTC 进行了检测,81 个中的 12 个(14.8%)为阳性。平均随访时间为 1.5 年。6 名(4.6%)同时患有经典甲状腺乳头状癌的患者在 NIFTP 诊断时发生局部淋巴结转移,111 名 EFVPTC 患者中有 15 名(13.5%)发生转移。34 名中的 6 名(14.7%)CPTCPFA 发生局部淋巴结转移,其中 5 名被认为是原发性病变。1 名 EFVPTC(0.9%),BRAFVE 阴性,转移至股骨。这些发现表明,与常规滤泡模式肿瘤取样相结合,使用 BRAFVE 是一种有用的诊断辅助手段。