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Polymerase chain reaction-based microsatellite analysis of fine-needle aspirations from Hürthle cell neoplasms.

作者信息

Takiyama Y, Saji M, Clark D P, Phillips G S, Segev D L, Smallridge R C, Westra W H, Udelsman R, Zeiger M A

机构信息

Department of Surgery, Johns Hopkins Medical Institutions, Baltimore, Maryland 21287-8611, USA.

出版信息

Thyroid. 1997 Dec;7(6):853-7. doi: 10.1089/thy.1997.7.853.

Abstract

Fine-needle aspiration (FNA) of the thyroid is the sine qua non in the preoperative evaluation of thyroid nodules. Despite this, cytological examination of FNA cannot differentiate malignant from benign Hürthle cell neoplasms. We have previously shown that Hürthle cell carcinomas harbor more genetic alterations on chromosomal arms 1q and 2p than Hürthle cell adenomas, and that all Hürthle cell neoplasms have a significantly higher frequency of alterations on chromosomal arm 1p compared with normal thyroid. To determine if these genetic alterations could be detected in FNA samples, we examined DNA from FNAs that were available from eight Hürthle cell neoplasms. Polymerase chain reaction (PCR) amplification of DNA demonstrated either direct correlation with alterations seen in the tumor samples or in some instances, additional chromosomal alterations. We conclude that PCR-based microsatellite DNA analysis of preoperative FNA samples from Hürthle cell neoplasms can potentially distinguish Hürthle cell carcinomas from adenomas and that with further validation and perfection, this technique may allow more optimal surgical management of patients with these lesions.

摘要

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