Please use this identifier to cite or link to this item: https://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/3792
Journal Title: Thyroid Hormone Resistance, a Case Report
Endocrine Society of Australia Annual Scientific Meeting 2015. Adelaide, SA Australia.
Authors: Watts, Anna K.
Gome, James, J.
SWH Author: Gome, James, J.
Keywords: Thyroid Hormone Resistance
Human
Case Report
Society
Australia
Patient
Goiter
Thyroid Disease
Family History
Hormone
Thyrotropin Secreting Adenoma
Hyperthyroxinemia
Hypophysis Adenoma
Nuclear Magnetic Resonance Imaging
Thyroid Function Test
Female
Euthyroidism
Hypothyroidism
Computer Assisted Tomography
Brain
Differential Diagnosis
Claustrophobia
Vascular Resistance
Tissues
Thyroidectomy
Hypoparathyroidism
Mutation
Thyrotoxicosis
Autosomal Dominant Inheritance
Father
Lymphocytic Infiltration
Gene
Live Birth
Hyperplasia
Histology
Clinical Feature
Thyroid Gland
Male
Protirelin Test
Thyrotropin
Thyroxine
Thyroid Hormone
Hormone
Protirelin
Liothyronine
Thyroid Hormone Receptor Beta
Issue Date: 2016
Date Accessioned: 2023-04-12T02:10:01Z
Date Available: 2023-04-12T02:10:01Z
Url: https://dx.doi.org/10.1111/cen.13010
Description Affiliation: A.K. Watts, Department of Endocrinology and Diabetes, St Vincent's Hospital, Melbourne J.J. Gome Department of Medicine, South West Healthcare, Warrnambool
Format Startpage: 47
Source Volume: 84
Issue Number: Supplement 1
DOI: https://dx.doi.org/10.1111/cen.13010
Date: 2016
Abstract: Introduction: Thyroid hormone resistance is a rare but important differential to consider in patients with hyperthyroxinaemia. The clinical presentation is that of non-suppressed thyroid stimulating hormone (TSH), elevated thyroid hormone levels and goitre with minimal clinical symptoms of thyrotoxicosis. The differential diagnosis for this hormone profile is TSH secreting pituitary adenoma. Case Report: A 31-year old woman presented with long standing deranged thyroid function tests in the setting of a strong paternal family history of thyroid disease. At the time of initial presentation at age 15, she had a goitre and markedly elevated triiodothyronine (T3) (16.3 pmol/L) and thyroxine (T4) (42.7 pmol/L) levels with a non-suppressed thyroid stimulating hormone (TSH) level (1.79 m/L). A computed tomography (CT) study of her brain, performed in lieu of magnetic resonance imaging (MRI) due to claustrophobia, did not demonstrate a pituitary adenoma. She went on to have a thyrotropin releasing hormone (TRH) test (200 mug IV TRH), which demonstrated an appropriate rise in TSH (12.34 mU/L at 20 min, 10.41 mU/L at 30 min). At the age of 26 she underwent a total thyroidectomy, complicated by transient hypoparathyroidism. Thyroid histology showed diffuse hyperplasia but no lymphocytic infiltration. She has subsequently required thyroxine replacement, with varying doses. She has a significant family history for thyroid disease, affecting multiple primary and secondary relatives on her father's side. Discussion(s): Thyroid hormone resistance is a rare autosomal dominant condition involving a mutation of the thyroid hormone receptor beta gene. It is estimated to occur in 1 in 40,000 live births. These patients have resistance to thyroid hormone in peripheral tissues. Variability of peripheral resistance means patients can have mixed clinical features of both hyper and hypothyroidism. These patients generally require supraphysiological replacement doses of thyroxine to achieve a relatively euthyroid state with TSH suppression.
URI: https://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/3792
Journal Title: Clinical Endocrinology
Type: Conference Paper
Conference Name: Endocrine Society of Australia Annual Scientific Meeting 2015.
Conference Location: Adelaide, SA Australia.
Appears in Collections:SWH Staff Publications

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