具有奇异细胞核和野生型P53表达的滤泡腺瘤:一例报告和文献复习。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2023-10-28 eCollection Date: 2023-01-01 DOI:10.1177/20363613231212383
Daniel Nguyen, Nyein Nyein Htun, Beverly Wang
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引用次数: 0

摘要

简介:甲状腺癌症是人类最常见的内分泌肿瘤。毛囊腺瘤/癌是第二常见的亚型。已经确定了多种组织学模式。具有奇异细胞核的滤泡腺瘤是与p53突变相关的模式之一,其临床预后尚不清楚。病例报告:一名74岁女性,偶然发现TSH水平升高和甲状腺标志物正常。超声检查显示双侧甲状腺多个结节,直径达1.9厘米。细针抽吸,细胞学检查显示一个Bethesda 5类结节。甲状腺全切除并颈清扫,病理显示滤泡性腺瘤伴奇异细胞核。根据免疫组织化学的结果,肿瘤细胞表现出野生型p53的染色和低水平的增殖指数Ki-67。结论:我们报道了一例罕见的甲状腺滤泡腺瘤,其细胞核奇异。与之前关于该肿瘤的报道相反,我们的患者使用免疫组织化学显示了p53野生型模式。需要更多的研究来更好地了解这种肿瘤的病因和临床预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Follicular adenoma with bizarre nuclei and wild-type P53 expression: A case report and literature review.

Introduction: Thyroid cancer is the most common endocrine tumor in humans. Follicular adenoma/carcinoma is the second most common subtype. Multiple histological patterns have been identified. Follicular adenoma with bizarre nuclei is one of the patterns associated with p53 mutation and has an unclear clinical prognosis.

Case report: A 74-year-old female presented with incidental findings of elevated TSH levels and normal thyroid markers. Ultrasound was performed and revealed multiple bilateral thyroid nodules measuring up to 1.9 cm. Fine needle aspiration was performed, and cytology showed one Bethesda category 5 nodule. Total thyroidectomy with neck dissection was performed, and the pathology showed follicular adenoma with bizarre nuclei. Based on the results of immunohistochemistry, the neoplastic cells exhibited staining for wild-type p53 and low levels of the proliferation index Ki-67.

Conclusions: We report a rare case of thyroid follicular adenoma with bizarre nuclei. In contrast to previous reports of this tumor, our patient showed a p53 wild-type pattern using immunohistochemistry. More studies are needed to better understand the etiology and clinical prognosis of this tumor.

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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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