| Literature DB >> 26622613 |
Xing Yu1, Yong Wang1, Ping Wang1, Cai-Hong Ji2, Chun-DI Miao2, Shu Zheng3.
Abstract
Primary thyroid paraganglioma (TP) is an uncommon tumor, and in rare cases, this disease tends to mimic medullary thyroid carcinoma (MTC). The present study reports a rare case of primary TP mimicking thyroid carcinoma, accompanied by hyperthyroidism. A 30-year-old female presented with an anterior cervical mass. Pre-operative radiological studies and operative frozen section analysis indicated an atypical MTC. Primary TP was finally diagnosed by pathology and immunohistochemical staining. Laboratory examinations (thyroid hormones tests) and Tc99m emission computed tomography revealed hyperthyroidism. Gene analysis of TP-associated gene mutations was negative. Surgical resection was performed as a curative approach and there is currently no metastasis after 36 months of follow-up. Surgeons must be aware of this disease in order to ensure a correct diagnosis and to prevent them from performing unnecessary procedures. The current study presents a case of primary TP mimicking MTC, discusses the radiographic results and histological characteristics, and provides a review of the associated literature.Entities:
Keywords: histological characteristics; hyperthyroidism status; medullary thyroid carcinoma; radiographic results; thyroid paraganglioma
Year: 2015 PMID: 26622613 PMCID: PMC4509088 DOI: 10.3892/ol.2015.3292
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967