Autonomously functioning thyroid nodule associated with thyrotoxic periodic paralysis.

Abstract:

:Thyrotoxic periodic paralysis (TPP) is mainly associated with Graves' disease but rarely with autonomously functioning thyroid nodule (AFTN). We herein report a case of AFTN associated with TPP in which the latter resolved after (131) I therapy for the former. We analyzed the genes encoding thyrotropin receptor (TSHR), the alpha-subunit of the stimulatory G protein (Gsalpha), calcium channel CACNA1S and potassium channel KCNE3, and found that the patient does not carry the known mutations in these genes. Whereas the pathogenesis of TPP and AFTN remains to be understood, the present case suggests that ion channel defects responsible for familial hypokalemic periodic paralysis may not be associated with TPP, and that mutations in TSHR and Gs alpha genes may be less frequent in AFTN patients in the Japanese population.

journal_name

Endocr J

journal_title

Endocrine journal

authors

Ozaki H,Mori K,Nakagawa Y,Hoshikawa S,Ito S,Yoshida K

doi

10.1507/endocrj.k07e-017

subject

Has Abstract

pub_date

2008-03-01 00:00:00

pages

113-9

issue

1

eissn

0918-8959

issn

1348-4540

pii

JST.JSTAGE/endocrj/K07E-017

journal_volume

55

pub_type

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