筛状-摩尔样甲状腺癌:一种罕见的肿瘤。

Q4 Medicine
Ceskoslovenska patologie Pub Date : 2022-01-01
Udmila Michnová, Eva Traboulsi, Barbora Peková, Aleš Ryška
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引用次数: 0

摘要

我们报告了一例51岁的患者,他接受了甲状腺全切除术,切除了右侧甲状腺叶,以治疗最大结节的生长进展,并进行了细针穿刺活检(FNAB),细胞学上怀疑是恶性肿瘤。结节是一种灰白色的固体状肿瘤,在组织学上具有异常的形态和免疫特征,称为筛状甲状腺结节癌(CMTC)。通常,肿瘤表现惰性,预后良好。CMTC可为家族性或散发性,主要为单发或多灶性病变,常与常染色体显性性腺瘤性息肉病综合征(FAP)相关,因此报告中有必要指出这一点。排除家族性腺瘤性息肉病综合征,APC基因突变为体细胞性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cribriform - morular thyroid carcinoma: a rare entity.

We present a case report of a 51-year-old patient who underwent totalization of thyroidectomy - resection of the right thyroid lobe for growth progression of the largest nodule from which a fine needle aspiration biopsy (FNAB) was performed and was cytologically suspected of malignancy. Nodule was a graywhite colored tumor with a solid structure, histologically with an unusual morphology and immunoprofile, called cribriform morular thyroid carcinoma (CMTC). Usually, the tumor behaves indolently with a good prognosis. CMTC can be familial or sporadic, predominantly as a solitary or a multifocal lesion, often associated with autosomal dominant adenomatous polyposis syndrome (FAP), so it is necessary to point this out in the report. The syndrome of familial adenomatous polyposis was ruled out, the APC gene mutation was somatic.

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来源期刊
Ceskoslovenska patologie
Ceskoslovenska patologie Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
17
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