Molecular Pathogenesis of Euthyroid and Toxic Multinodular Goiter
Молекулярный патогенез эутиреоидного и токсического многоузлового зоба
2004-12-22
SCID: 54.1/wxmyssgd
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euthyroid multinodular goitermutagenesissomatic mutationsthyroid hyperplasiatoxic multinodular goiter
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Abstract (AI)
The purpose of this review is to summarize current knowledge of the etiology of euthyroid and toxic multinodular goiter (MNG) with respect to the epidemiology, clinical characteristics, and molecular pathology. In reconstructing the line of events from early thyroid hyperplasia to MNG we will argue the predominant neoplastic character of nodular structures, the nature of known somatic mutations, and the importance of mutagenesis. Furthermore, we outline direct and indirect consequences of these somatic mutations for thyroid pathophysiology and summarize information concerning a possible genetic background of euthyroid goiter. Finally, we discuss uncertainties and open questions in differential diagnosis and therapy of euthyroid and toxic MNG.
Key Findings
1
Known somatic mutations in thyroid tissue play a significant role in the molecular pathology and pathophysiology of both euthyroid and toxic MNG.
2
Multinodular goiter (MNG) development follows a sequence from early thyroid hyperplasia to nodular structures with predominantly neoplastic character.
3
Mutagenesis is an important factor contributing to the emergence and progression of nodules in MNG.
4
Significant uncertainties remain in differential diagnosis and therapy choices for euthyroid versus toxic MNG.
5
There is evidence for a possible genetic background contributing specifically to euthyroid goiter.
Research Object
Euthyroid and toxic multinodular goiter (MNG)
Research Subject
Molecular pathogenesis including somatic mutations, mutagenesis, neoplastic character of nodules, and consequences for thyroid pathophysiology, epidemiology, clinical features, and implications for differential diagnosis and therapy
Publication Details
Publication Date
2004-12-22
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