|Year : 2016 | Volume
| Issue : 2 | Page : 460-462
Not all elevated hormones are toxic: A case of thyroid hormone resistance
Rajeev Philip1, Mohan Krishnakumar Padikal2, Altaf Alinausad3, Charamelsankaran Keshavan3
1 Department of Endocrinology, PIMS, Thiruvalla, Kerala, India
2 Department of Family Medicine, PIMS, Thiruvalla, Kerala, India
3 Department of Medicine, PIMS, Thiruvalla, Kerala, India
|Date of Web Publication||18-Oct-2016|
Department of Endocrinology, PIMS, Thiruvalla, Kerala
Source of Support: None, Conflict of Interest: None
Resistance to thyroid hormone syndrome (RTH) is a rare disorder and is usually inherited as dominantly negative autosomal trait. RTH is caused by mutations in the thyroid hormone receptor beta. Patients with RTH usually do not have signs and symptoms of thyrotoxicosis, but the thyroid function test shows an elevated T3 and T4, which get misinterpreted as hyperthyroidism, resulting in unnecessary treatment.
Keywords: Neurophysiologic abnormalities, resistance to thyroid hormone syndrome, thyroid hormone receptor beta
|How to cite this article:|
Philip R, Padikal MK, Alinausad A, Keshavan C. Not all elevated hormones are toxic: A case of thyroid hormone resistance. J Family Med Prim Care 2016;5:460-2
|How to cite this URL:|
Philip R, Padikal MK, Alinausad A, Keshavan C. Not all elevated hormones are toxic: A case of thyroid hormone resistance. J Family Med Prim Care [serial online] 2016 [cited 2021 May 14];5:460-2. Available from: https://www.jfmpc.com/text.asp?2016/5/2/460/192339
| Introduction|| |
Thyroid hormone resistance (RTH) is a rare genetic disorder characterized by reduced target tissue responsiveness to thyroid hormones. Since Refetoff et al. described this syndrome in 1967; over 1000 cases have been identified. Thyroid hormone resistance can have highly variable clinical manifestations, making it difficult to diagnose, and it may go unrecognized for a long time, or can get misdiagnosed and treated as hyperthyroidism.
We are presenting the case of a 26-year-old female with goiter and RTH and was managed previously as a case of hyperthyroidism.
| Case Report|| |
A 26-year-old female was referred to the medicine OPD for follow-up of her thyroid status. She was previously diagnosed to have hyperthyroidism from an outside hospital and was on carbimazole for the last 5 years.
On review of her complaints, she recollected that she was always the shortest in her class in the school years. There was also a history of subnormal intelligence, poor scholastic performance, hearing loss, and attention deficit hyperactivity disorder (ADHD). There was a history of short stature in the family in the maternal side, and they were being treated for hyperthyroidism. She developed goiter 10 years back, but she did not have any clinical symptoms of hyperthyroidism (palpitations, tremors, and moist skin) nor had any ocular signs or symptoms. During the evaluation for goiter, her thyroid hormone levels showed increased T4, T3, free T4 and free T3, with a normal thyroid stimulating hormone (TSH), for which she was started on antithyroid drugs.
On clinical examination, she was conscious and alert, short statured (height 142 cm, weight 47 kg). She had tachycardia with a pulse rate of 102/min. She was normotensive and afebrile at presentation. Examination of the thyroid gland showed diffuse enlargement of the thyroid, World Health Organization Grade 2 without palpable nodules [Figure 1]. There was no bruit on auscultation, and the eye examination was normal. The systemic examination was within normal limits.
Laboratory investigations showed elevated T3 and T4 with T3 - 3.15 (0.95–2.5 nmol/L), free T3 - 5.12 (2.3–4.2 pg/mL), T4: 233 (60–120 nmol/L), and free T4 - 3.1 (0.8–1.8 ng/L). The TSH was inappropriately normal - 4.39 (0.2–5 µIU/L).
Ultrasonography thyroid was done which showed multiple hyperechoic well-defined subcentimetric nodules with peripheral halo and no internal vascularity in both lobes of the thyroid-features suggestive of multinodular goiter.
The possibilities of thyroid hormone resistance and TSH-secreting adenoma were considered, and a magnetic resonance imaging (MRI) pituitary was done to look for a pituitary mass, which turned out to be normal. A sex hormone binding globulin levels were done to look for peripheral action of thyroid hormone, which was normal - 48.3 ng/L (normal - 11.7–137.2 ng/L), indicating the resistance of thyroid hormone action at the level of liver.
A pure tone audiometry done showed a moderate hearing loss with mixed component at mid frequency [Figure 2].
Thyroxin suppression testing was done which showed poor suppression of TSH (3.29 µIU/L), confirming the diagnosis of thyroid hormone resistance.
| Discussion|| |
RTH is found in about 1/40,000–50,000 live births. Familial occurrence of RTH has been documented in approximately 75% of cases and inheritance is usually autosomal dominant, but de novo mutation can occur in approximately 17% of cases. Both males and females are equally affected.
RTH is classified into two phenotypes: Generalized resistance to thyroid hormone (GRTH) and partial resistance to thyroid hormone (PRTH). Patients with GRTH are typically euthyroid or hypothyroid, whereas patients with PRTH are usually hypermetabolic. No differences in the absolute levels of TSH or free thyroid hormone are observed in GRTH patients as opposed to PRTH patients. A molecular mechanism to explain these two clinical phenotypes has proven elusive, and many authors have concluded that they are part of a spectrum of the same disorder.
Sinus tachycardia is very common in patients with RTH, some studies reporting frequency as high as 80%. The liver and pituitary express predominantly thyroid hormone receptor beta 1 (TRβ) and TRβ2 respectively, whereas myocardium expresses TRα1. Therefore, mutations in the TRβ gene in RTH are associated with pituitary and liver resistance, as exemplified by normal serum sex-hormone-binding globulin and nonsuppressed TSH levels seen in patients while the tachycardia seen in many RTH cases may represent retention of cardiac sensitivity to elevated thyroid hormones acting via a normal TRα., Most cases of RTH are caused by mutations in the THRB gene.
Neurophysiological abnormalities such as ADHD in childhood or language development problems manifested by poor reading skills, dyslexia, and problems with articulation have been documented in a large number of patients with RTH.
The diagnosis of thyroid hormone resistance is suspected when a patient with no features of hyperthyroidism is detected to have elevated free T3 and free T4 with normal or slightly elevated TSH. A normal MRI Pituitary, a normal SHBG levels, and nonsuppressible TSH after thyroxine or liothyronine will help to confirm the diagnosis. This diagnosis helps in avoiding unnecessary treatment as most of the patients get treated as hyperthyroidism, as it happened in our case.
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Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]