Endoperspectives, Volume 4, Issue 3
ثبت نشده
چکیده
Thyroid nodules are a common problem found in up to two-thirds of the population on ultrasound examination. Nodules are often encountered incidentally on exams performed for other purposes. The prevalence increases with age and with radiation exposure and is higher amongst women. Approximately 5-15% of nodules are malignant; therefore, deciphering which nodules warrant attention is important. Factors that increase a nodules’ likelihood of being malignant include: history of radiation exposure, male patient, age over 45 years and family history amongst others (Table 1). A thyroid nodule is a discrete lesion seen within the thyroid gland that is distinct from the surrounding thyroid parenchyma. Thyroid nodules can be discovered on palpation or ultrasonographic examination or other imaging modalities (CT, MRI or FDG-PET scan etc). Nonpalpable nodules discovered by imaging modalities done for other purposes are often termed “incidentalomas”. Workup of Thyroid Nodules When the thyroid nodule is discovered, a complete history and physical examination should be performed. A pertinent history should include: history of thyroid disease, history of thyroid cancer or thyroid cancer syndromes (familial polyposis, cowden’s, carney’s, multiple endocrine neoplasias), and hoarseness. On physical exam, one should note the size of the thyroid and the nodules, associated lymphadenopathy, associated fixation of nodules to surrounding structures, signs of thyrotoxicosis and vocal cord paralysis. Laboratory and radionuclide investigation Once thyroid nodules are discovered, a serum TSH should be checked. If the serum TSH is suppressed, then a radionuclide thyroid scan is performed to determine if the nodule of interest is a “hot” nodule. Radionuclide scans include either technetium 99mTc pertechnetate scans or 123I scans. “Hot” nodules are indicative that the nodule is hyperfunctioning and tracer uptake is greater than the surrounding normal thyroid. Given that “hot” nodules rarely harbor malignancy, biopsy of these nodules is not usually warranted. Treatment for thyrotoxicosis should then ensue.
منابع مشابه
Endoperspectives, Volume 3, Issue 2
Hereditary medullary thyroid carcinoma (MTC) presents within the context of 3 genetic syndromes. Multiple endocrine neoplasia type 2A (MEN2A, Sipple’s syndrome) is an autosomal-dominant genetic syndrome that includes MTC, pheochromocytoma, and primary hyperparathyroidism (PHPT). MEN2B is an autosomal-dominant genetic syndrome that includes MTC, pheochromocytoma, multiple mucosal neuromas, and a...
متن کاملEndoperspectives, Volume 5, Issue 3
The World Health Organization defines pheochromocytoma (PHEO) as a tumor arising from the adrenal medulla and paraganglioma (PGL) as a tumor arising from the paraganglia outside the adrenal medulla. PGLs are located in the head, neck, thorax, abdomen, and pelvis, and can be classified as parasympathetic and sympathetic depending on their origin. Parasympathetic PGLs are mainly located in the he...
متن کاملOn the Performance of Cooperative Spectrum Sensing of Cognitive Radio Networks in AWGN and Rayleigh Fading Environments
| PDF (1174 Kbytes) ■ Sub-channel Allocation Based on Multi-level Priority in OFDMA Systems 1876 1889 JongChan Lee, MoonHo Lee Abstract | PDF (562 Kbytes) ■ Robust Backup Path Selection in Overlay Routing with Bloom Filters 1890 1910 http://www.itiis.org/tiis/content_view_articles.jsp?vol=0&userid= 1 -> 3 08.09.2013 13:58 Xiaolei Zhou, Deke Guo, Tao Chen and Xueshan Luo Abstract | PDF (1483 Kby...
متن کاملScienceDirect - Food Microbiology, Volume 24, Issues 7-8, Pages 671-808 (October-December 2007)
Articles in Press Volume 24 (2007) Volume 24, Issues 7-8 pp. 671-808 (October-December 2007) Volume 24, Issue 6 pp. 549-670 (September 2007) Volume 24, Issue 5 pp. 433-548 (August 2007) Volume 24, Issue 4 pp. 313-432 (June 2007) Volume 24, Issue 3 pp. 197-312 (May 2007) Volume 24, Issue 2 pp. 113-196 (April 2007) 3rd International Symposium on Sourdough, 3rd International Symposium on Sourdough...
متن کامل