Reversible Pituitary Enlargement in the Syndrome of Resistance to Thyroid Hormone

We report pituitary enlargement after radioiodine ablation in a patient with elevated thyroid hormones and features of hyperthyroidism. Serum thyrotropin (TSH) levels were elevated despite normal circulating thyroid hormones, suggesting inappropriate TSH secretion associated either with a TSH secret...

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Veröffentlicht in:Thyroid (New York, N.Y.) N.Y.), 1998-08, Vol.8 (8), p.679-682
Hauptverfasser: Gurnell, M, Rajanayagam, O, Barbar, I, Jones, M K, Chatterjee, V K
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container_issue 8
container_start_page 679
container_title Thyroid (New York, N.Y.)
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creator Gurnell, M
Rajanayagam, O
Barbar, I
Jones, M K
Chatterjee, V K
description We report pituitary enlargement after radioiodine ablation in a patient with elevated thyroid hormones and features of hyperthyroidism. Serum thyrotropin (TSH) levels were elevated despite normal circulating thyroid hormones, suggesting inappropriate TSH secretion associated either with a TSH secreting pituitary adenoma or resistance to thyroid hormone (RTH). Normal serum glycoprotein α-subunit levels and a preserved TSH response to thyrotropin-releasing hormone (TRH) favored RTH and this diagnosis was confirmed by showing the patient to be heterozygous for a missense mutation (R438H) in the thyroid hormone β receptor (TRβ) gene. Thyroxine replacement in supraphysiological doses were required to normalize TSH levels and resulted in regression of the pituitary enlargement, suggesting hyperplasia rather than coincident tumor. This case illustrates the need to avoid thyroid ablation in RTH patients and the importance of supraphysiological thyroxine replacement to prevent pituitary hyperplasia.
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Serum thyrotropin (TSH) levels were elevated despite normal circulating thyroid hormones, suggesting inappropriate TSH secretion associated either with a TSH secreting pituitary adenoma or resistance to thyroid hormone (RTH). Normal serum glycoprotein α-subunit levels and a preserved TSH response to thyrotropin-releasing hormone (TRH) favored RTH and this diagnosis was confirmed by showing the patient to be heterozygous for a missense mutation (R438H) in the thyroid hormone β receptor (TRβ) gene. Thyroxine replacement in supraphysiological doses were required to normalize TSH levels and resulted in regression of the pituitary enlargement, suggesting hyperplasia rather than coincident tumor. 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subjects Female
Humans
Hyperthyroidism - radiotherapy
Hypertrophy - diagnosis
Hypertrophy - etiology
Hypertrophy - physiopathology
Iodine Radioisotopes - therapeutic use
Magnetic Resonance Imaging
Middle Aged
Pituitary Gland - pathology
Pituitary Gland - physiopathology
Point Mutation
Receptors, Thyroid Hormone - genetics
Thyroid Gland - radiation effects
Thyroid Hormone Resistance Syndrome - complications
Thyroid Hormone Resistance Syndrome - drug therapy
Thyroid Hormone Resistance Syndrome - genetics
Thyrotropin - blood
Thyrotropin-Releasing Hormone - blood
Thyroxine - therapeutic use
Tomography, X-Ray Computed
title Reversible Pituitary Enlargement in the Syndrome of Resistance to Thyroid Hormone
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