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"Colloid-Rich" follicular neoplasm/suspicious for follicular neoplasm thyroid fine-needle aspiration specimens: Cytologic, histologic, and molecular basis for considering an alternate view.

富于胶质的滤泡性肿瘤/疑为滤泡性肿瘤的甲状腺细针穿刺活检标本:有关其细胞学、组织学和分子机制的新观点。

Ohori NP,Wolfe J,Hodak SP,Lebeau SO,Yip L,Carty SE,Duvvuri U,Schoedel KE,Nikiforova MN,Nikiforov YE

Abstract

Typically, thyroid follicular neoplasm/suspicious for follicular neoplasm (FN/SFN) cases show moderate to marked cellularity and scant or absent colloid. Recently, cases have been noted with microfollicular cellularity in the background of moderate to abundant amount of colloid. The purpose of this study was to compare these "colloid-rich" FN/SFN cases to the typical FN/SFN cases.
Thyroid cytology specimens with the features of FN/SFN were searched in cytopathology files from September 2008 to June 2012. Cases with absent or minimal colloid were designated "typical colloid-poor" FN/SFN and cases with moderate to abundant colloid were designated "colloid-rich" FN/SFN. From these cases, those with surgical pathology resection follow-up were identified. Cytologic, surgical pathology resection, and molecular features (BRAF, RAS, RET/PTC, and PAX8-PPARγ) were investigated for the typical colloid-poor FN/SFN cases and were compared with those of the colloid-rich FN/SFN cases.
Of 431 FN/SFN cases with surgical pathology resection follow-up, 360 (83.5%) cases showed features of typical colloid-poor FN/SFN and 71 (16.5%) cases showed features of colloid-rich FN/SFN. Papillary carcinoma was the most common malignant outcome for the 2 groups. Although the proportion of malignant outcome was similar for the 2 groups, the "colloid-rich" FN/SFN cases showed a greater proportion of nodular hyperplasia among the cases with benign outcome. In addition, the "colloid-rich" FN/SFN cases demonstrated a greater proportion of cases with a mutation.
Approximately one-sixth of cases of FN/SFN show "colloid-rich" features. Comparison to the typical colloid-poor FN/SFN demonstrated similar risk for malignancy but contrasting resection outcome and molecular characteristics. Cancer (Cancer Cytopathol) 2013;121:718-728. © 2013 American Cancer Society.

摘要

 背景:通常,滤泡性肿瘤/疑为滤泡性肿瘤的病例,细胞中-显着密集,而胶质稀少或缺乏。最近,有病例提到了伴有中-丰富的胶质的微滤泡结构。本研究旨在比较富于胶质的滤泡性肿瘤/疑为滤泡性肿瘤与经典型滤泡性肿瘤/疑为滤泡性肿瘤的区别。
方法:收集2008年9月到2012年6月的具有滤泡性肿瘤/疑为滤泡性肿瘤特征的甲状腺细胞学标本。胶质稀少或缺乏的病例被归为“经典的胶质缺乏型”滤泡性肿瘤/疑为滤泡性肿瘤,而具有中-丰富胶质的病例则被归为“胶质丰富型”滤泡性肿瘤/疑为滤泡性肿瘤。从这些病例中,找出那些后面进行了外科手术切除术的病例。我们研究了经典型胶质稀少或缺乏的滤泡性肿瘤/疑为滤泡性肿瘤病例的细胞学、外科切除标本及分子学特征(BRAF,RAS,RET/PTC,PAX8-PPARγ),并与“胶质丰富型”滤泡性肿瘤/疑为滤泡性肿瘤进行比较。
在431例进行了外科手术切除标本病理检查的滤泡性肿瘤/疑为滤泡性肿瘤病例中,360例(8.5%)显示出经典的胶质缺乏型”滤泡性肿瘤/疑为滤泡性肿瘤的特征,71例(16.5%)显示出富于胶质型滤泡性肿瘤/疑为滤泡性肿瘤的特征。这两组病例最常见的恶性结果是发展成为乳头状癌,尽管两组恶变的比例是一样的,但富于胶质的滤泡性肿瘤/疑为滤泡性肿瘤在那些具有良性结局的病例中表现为结节状增生的比例更大。此外,富于胶质的滤泡性肿瘤/疑为滤泡性肿瘤发生突变的比例更大。
大约有1/6的滤泡性肿瘤/疑为滤泡性肿瘤显示出胶质丰富的特征,与经典的胶质缺乏型滤泡性肿瘤/疑为滤泡性肿瘤相比,恶变的风险相同,但切除的结果和分子学特征却有明显差异。

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