Literature DB >> 19189692

Thyroidectomy in a patient with multinodular dyshormonogenetic goitre--a case of Pendred syndrome confirmed by mutations in the PDS/SLC26A4 gene.

Karolina Banghova1, Ondrej Cinek, Eva Al Taji, Jirina Zapletalova, Radan Vidura, Jan Lebl.   

Abstract

We report a young woman with genetically confirmed Pendred syndrome and discuss the current therapeutic strategies of dyshormonogenetic goitre. A small diffuse thyroid enlargement developed during infancy and although substitution therapy with L-thyroxine was adequate, it progressed and underwent multinodular transformation. Cervical ultrasound at the age of 22 years demonstrated three solid nodules and fine-needle aspiration biopsy showed a finding typical of follicular adenoma. It is known that dyshormonogenetic goitres have a tendency to grow despite appropriate treatment with L-thyroxine. Management of a patient with Pendred syndrome requires careful follow-up and regular imaging of the thyroid. Although the therapeutic approach to dyshormonogenetic goitres is still controversial, in our patient we chose total thyroidectomy as the most advantageous method to prevent the development of malignancies that may arise more frequently from dyshormonogenetic goitres than from goitres of other aetiologies.

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Year:  2008        PMID: 19189692     DOI: 10.1515/jpem.2008.21.12.1179

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  1 in total

1.  Delayed diagnosis of Pendred syndrome.

Authors:  Natalie Smith; Jean-Marie U-King-Im; Janaka Karalliedde
Journal:  BMJ Case Rep       Date:  2016-09-12
  1 in total

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