Exp Clin Endocrinol Diabetes 2006; 114(5): 235-239
DOI: 10.1055/s-2006-924239
Article

J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

Incidence of Radioiodine Induced Graves' Disease in Patients with Multinodular Toxic Goiter

J. Meller1 , U. Siefker1 , A. Hamann1 , M. Hüfner2
  • 1Department of Nuclear Medicine, University of Göttingen, Göttingen, Germany
  • 2Department of Internal Medicine, University of Göttingen, Göttingen, Germany
Further Information

Publication History

Received: September 1, 2005 First decision: October 24, 2005

Accepted: November 28, 2005

Publication Date:
28 June 2006 (online)

Abstract

In this study, we assessed the incidence of Graves' disease (GD) following radioiodine therapy (RIT) in a large cohort of well characterized patients with autonomy in comparison to the clinical course of control patients with thyroidal autonomy not definitively treated with 131I or surgery. 622 consecutive patients were treated with 131I for autonomy (unifocal: n = 321; multifocal: n = 199; disseminated: n = 102) and followed up for at least 6 months post RIT. 108 consecutive patients with autonomy not definitively treated (unifocal: n = 49; multifocal: n = 42; disseminated: n = 11) followed up for at least 6 months served as controls. Initial evaluation and follow-up included determination of FT3, FT4, TSH, autoantibodies against the thyroid peroxidase (anti-TPO) and TSH-receptor antibodies (TRAb) by highly sensitive radio receptor-assay, quantitative thyroid scintigraphy and sonography. After 6 months, GD was newly diagnosed in 1/321 patients with unifocal autonomy, in 1/199 patients with multifocal autonomy and in 0/108 control patients. In patients with disseminated autonomy (group C), GD was diagnosed significantly more often compared to the other groups (5/102 patients; 4,1 %; p < 0.05). In conclusion, RIT may induce Graves' disease in a few cases with toxic multinodular goiter. The incidence in this population is small. Compared with patients suffering from uni- or multifocal autonomy, subjects with disseminated autonomy have a more than tenfold higher risk for the development of GD.

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MD Johannes Meller

Department of Nuclear Medicine
Georg August University

Robert-Koch-Str. 40

37075 Göttingen

Germany

Phone: + 49551398510

Fax: + 49 551 39 85 26

Email: jmeller@med.uni-goettingen.de

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