Three cases with inappropriate TSH syndrome: uygunsuz TSH sendromlu Uc olgu.
In most patients with hyperthyroidism, [T.sub.3] and [T.sub.4] levels are high while thyroid-stimulating hormone (TSH) is too low to detect. Some patients may have inappropriately normal or elevated levels of TSH, which is called inappropriate secretion of TSH or central hyperthyroidism (1). Ones likely laboratory errors are excluded, the differential diagnosis should be between TSH-secreting pituitary adenoma (TSHoma) and thyroid hormone resistance (THR) in inappropriate TSH secretion (2). Although THR is usually an autosomal dominant disorder caused by mutations in the thyroid hormone receptor [beta] gene, 15% of the cases are sporadic (1), (3). Its incidence has been reported to be 1/50.000 (1). Patients with THR exhibit THR in the pituitary and/or peripheral tissues (4). Clinically, THR has two forms. In the first form known as generalized resistance to thyroid hormone (GRTH), pituitary and peripheral tissues show resistance to [T.sub.3] while in the second form known as pituitary resistance to thyroid hormone (PRTH), there is pituitary resistance to [T.sub.3] (5). In patients with PRTH, increased peripheral response to thyroid hormones has also been described (4).
Among conditions causing hyperthyroidism, TSHoma is considered to be extremely rare. This adenoma is present in less than 1% of pituitary adenoma patients. A possible explanation for being so rare is that thyrotropic cells comprise less than 5% of all pituitary cells (6). Its prevalence has been reported to be one in a million (1).
In this study, we discuss the differential diagnosis of 3 cases with inappropriate TSH syndrome.
A 29-year-old female patient presented with thyroid function disorder. In her history, laboratory tests revealed a serum free [T.sub.3] of 5.1 pg/ml (normal: 1.4-4.4 pg/ml), serum free T4 of 2.7 ng/dl (normal: 0.7-1.8 ng/dl) and serum TSH of 2.2 [micro]IU/ml (normal: 0.4-4.6 [micro]IU/ml). She was prescribed propylthiouracil (PTU) 150 mg tid per day. A month later, upon observing that FT4 had increased to 3.9 ng/dl, PTU dose was doubled. This was repeated every month and PTU dose was increased up to 600 mg tid per day. As euthyroidism was not achieved despite a high-dose PTU treatment, she was referred to our endocrinology department. In her physical examination, her thyroid gland was diffuse large. The patient was clinically euthyroid and there was no family history of thyroid disease. PTU treatment was then stopped. After 3 weeks, in the laboratory tests, F[T.sub.3] was 4.6 pg/ml, F[T.sub.4] was 2.7 ng/dl and TSH was 1.8 [micro]lU/ml. Thyroid autoantibodies including antimicrosomal autoantibodies and antithyroglobulin autoantibodies were negative. Ultrasonography revealed that both lobes were large while scintigraphy showed that the activity distribution increased homogeneously. In the TRH test, TSH responses were found as 1.4, 14.8 and 10.5 [micro]IU /ml during the 0th,30th and 60th minutes, respectively. In [T.sub.3] suppression test, 50 [micro]g, 100 [micro]g and 200 [micro]g of [T.sub.3], divided into two equal doses for each day, were administered to the patient respectively for three days. Peripheral markers of thyroid hormone response were analyzed during basal period and on the 3rd, 6th and 9th days; and they were found to be within the normal levels (Table 1). At the end of the test, TRH test was repeated; and TSH responses were found to be 0.08, 0.9 and 0.5 [micro]IU/ml during the 0th, 30th and 60th minutes, respectively, which was a two-fold increase. Magnetic resonance image (MRI) of the pituitary was normal. The thyroid function tests of the patient's first degree relatives -father and three siblings- were found to be normal. GRTH was considered in the patient, however, no treatment was recommended since the patient was clinically euthyroid.
Table 1. Results of the [T.sub.3] suppression tests Case 1 Case 3 Normal Baseline Day Day Day 9 Baseline Day Day 6 3 6 3 F[T.sub.3] 1.4-4.4 5.3 6.7 8.1 13.8 4.7 5.1 6.9 (pg/ml) F[T.sub.4] 0.7-1.8 2.9 2.3 1.8 1.7 1.5 1.4 1.1 (ng/dl) TSH (MIU/ml) 0.4-4.6 1.2 0.7 0.1 0.06 2.9 2.3 0.9 SHBG 30-100 14 - 14 - 159 194 198 (mmol/l) Cholesterol 125-350 172 147 157 - 106 110 109 (mg/dl) TG (mg/dl) 40-160 198 251 285 - 39 44 48 CPK (U/l) 24-195 33 34 46 51 89 97 90 Body weight - 69 68 69 68 52.5 52 53.5 (kg) Ferritin 13-400 58 70 88 88 35 36 36 (ng/ml) E2 (pg/m) 56 66 96 Day 9 F[T.sub.3] 11.7 (pg/ml) F[T.sub.4] 1.1 (ng/dl) TSH (MIU/ml) 0.2 SHBG - (mmol/l) Cholesterol 111 (mg/dl) TG (mg/dl) 40 CPK (U/l) 82 Body weight 53.3 (kg) Ferritin 49 (ng/ml) E2 (pg/m) 290
A 33-year-old female patient presented to another clinic with complaints of weight loss and menstrual irregularity. Her laboratory tests revealed a serum prolactin of 40.3 ng/mL (4.0-15.2 ng/mL); [T.sub.3] of 6.2 pg/ml, [T.sub.3] of 2.5 ng/ml and TSH of 6.2 [micro]IU/ml. PTU was started. After detecting a pituitary macroadenoma measuring 4 x 5 x 7 cm on pituitary MRI, transsphenoidal subtotal excision of pituitary adenoma was performed. She received postoperative radiotherapy and subsequently developed amenorrhea. Up to two months before contacting us, the patient had continued to take PTU. She presented to our endocrinology department with a complaint of amenorrhea. In her ultrasonography, the right thyroid lobe was measured 22 x 29 x 56 mm, and the left lobe was measured 21 x 24 x 53 mm in size. Laboratory results were as follows: F[T.sub.3]: 7.8 pg/ml, F[T.sub.4]: 3.1 ng/dl, TSH: 2.0 [micro]IU/ml, FSH: 2.6[micro]IU/ml, LH: 0.6 [micro]IU/ml, PRL: 15.8 ng/ml, Cortisol: 3.9[micro]g/dl, GH: 4.4 ng/ml (0.1-7.02), IGF-1:150 ng/ml (140-405), SHBG: 202 mmoI/l (30-100), TSH alpha subunit level: 1.32 mUI/ml(0.05-0.9), alpha subunit/ molar TSH: <1. TSH values measured in TRH stimulation test were: 0 minute: 2.2, 30 minutes: 2.2, 60 minutes: 2.3, 90 minutes: 2.5 and 120 minutes: 2.6. No sufficient response was observed to insulin tolerance test and GnRH test. The patient was diagnosed with TSHoma and panhypopituitarism as her SHGB, alpha subunit level, and alpha subunit/molar TSH ratio were high, there was no response to TRH test, and the patient had undergone surgery for pituitary macroadenoma previously. The patient was given a treatment with 20 mg octreotide LAR/once a month, 5 mg prednisolone/daily and cyclic estrogen-progesterone. The patient is currently euthyroid and on replacement therapy.
A 20-year-old female patient presented to the endocrinology outpatient clinic with the complaints of alopecia, weight loss (>1kg) and palpitation for the last one month. Her laboratory tests were as follows: F[T.sub.3]: 3.9 pg/ml, F[T.sub.4]: 1.5 ng/dl, TSH: 4.6 [micro]IU/ml. Her thyroid ultrasonography was normal in the presence of negative thyroid autoantibodies including antimicrosomal autoantibodies and antithyroglobulin autoantibodies. Pituitary MRI revealed a normal pituitary. TSH response to TRH was measured as: 0 minute: 2.8, 30 minutes: 9.8, 60 minutes: 10.6 [micro]IU/ml. The results of [T.sub.3] suppression test are shown in Table 1. TSH responses to TRH after [T.sub.3] suppression test were as follows: 0 minute: 0.9, 30 minutes: 2.9, 60 minutes: 2.6, 90 minutes: 1.8, 120 minutes: 1.2 [micro]IU/ml and SHBG: 185 mmoI/l. After the examinations carried out, the patient was diagnosed with PRTH. The patient was then prescribed [beta]-blocker and started to be followed up.
TSH is suppressed by thyroid hormones through negative feedback in the hypothalamic-pituitary-thyroid axis. In case of elevated serum levels of free thyroid hormones with non-suppressed TSH, one should suspect inappropriate TSH secretion. (1), (7). Once increased thyroxine-binding protein (TBG), presence of antibodies connected to T3 and [T.sub.4], amiodarone treatment, familial dysalbuminaemic hyperthyroxinaemia (FDH), high-dose or intermittent L-thyroxine treatment which are among other causes of inappropriate TSH release are ruled out, THR and TSHoma should be investigated (1), (2). In our three cases, F[T.sub.3] and F[T.sub.4] levels were high and TSH levels were not suppressed. After likely laboratory errors were excluded, differential diagnosis was made between TSHoma and THR.
THR is a rare genetic disorder. While both pituitary and peripheral tissues show resistance to [T.sub.3] in GRTH, pituitary shows resistance to [T.sub.3] in PRTH. In PRTH, hyperthyroidism features including heart (tachycardia) and brain (nervousness, insomnia, attention deficit, hyperactivity) symptoms may be present, nevertheless, the other organ systems may not be involved (8). In our cases, the patient with GRTH was clinically euthyroid while the patient with PRTH had hyperthyroidism symptoms such as palpitation, weight loss and alopecia. Although both of the forms are clinically different, they are genetically the same (5), (7), (9). Despite the fact that THR is usually an autosomal dominant disorder, 10-15% of cases can be sporadic (1), (10). Even though mutation analyses of TR[beta] gene provide early diagnosis of THR and, thus, prevent family members from being scanned unnecessarily, gene mutation analysis could not be performed in our patients and their families, however, thyroid function tests of the first degree relatives of the cases were normal and/or there was no history of thyroid gland disease.
TSHomas are rare pituitary tumors that cause hyperthyroidism by secreting TSH (5). Most of them are macroadenoma in the pituitary (6), (7), (11), as found in our case. Differential diagnosis should be made between TSHoma and THR, which are two significant causes of TSH syndrome. Differential diagnosis is important as the treatment of the central hyperthyroidism differ from each other. Patients with GRTH are frequently asymptomatic and are incidentally detected. Symptoms in some patients with GRTH can display clinical characteristics varying between hypothyroidism and hyperthyroidism (1), (9). However, our patient with GRTH (case 1) was clinically asymptomatic; she presented with a complaint of goiter and her diagnosis was made by examination.
In PRTH, hyperthyroidism symptoms are at the forefront as peripheral tissues respond to elevated thyroid hormone (1), (5). In TSHomas, hyperthyroidism and goiter are present; symptoms of cephalalgia, visual field defect and hypopituitarism can also be observed (1), (7). Our patient with TSHoma (case 2) had symptoms of hyperthyroidism in addition to the complaints of panhypopituitarism.
Peripheral markers of thyroid hormone like SHGB and angiotensin converting enzyme (ACE) are often elevated in TSHomas, however, they are usually normal in cases with THR (1). TSH [alpha]-subunit and [alpha]-subunit/ TSH molar ratio should be checked in such patients. While [alpha]-subunit level is high in 66% of those with TSHoma, [alpha]-subunit/TSH molar ratio is high in 80% of them. As [alpha]-subunit is also secreted along with LH and FSH, [alpha]-subunit/TSH molar ratio is a more specific test (1), (5), (7). In our case with TSHoma (case 2), [alpha]-subunit level ratio and [alpha]-subunit/TSH molar ratio were also high.
[T.sub.3] suppression test is important in the differential diagnosis between TSHoma and THR. [T.sub.3] is administered with increasing the dose every three days (50 [micro]g, 100 [micro]g, 200 [micro]g divided into two doses to be administered at 12 hour intervals). At the onset of the test and with each dose increment, peripheral markers such as serum cholesterol, triglyceride, creatine phosphokinase (CPK), ferritin, SHBG, prolactin, TSH, heart rate, urinary magnesium, and body weight are checked and TRH stimulation test is performed. While there is no significant change in parameters except heart rate and urine magnesium in cases with GRTH, these markers change in TSHoma as there is no peripheral resistance (9). An increase in the levels of SHGB, ferritin and E2 and, a slight decrease in CPK was detected in our patient with PRTH (case 3), whereas no change was observed in peripheral markers except for the slight increase in ferritin in our patient with GRTH (case 1). Because peripheral markers may be variable, other diagnostic procedures such as TRH test and pituitary MRI should be used in establishing an accurate diagnosis. After administration of a high-dose [T.sub.3], TSH levels are not suppressed in TSHoma whereas they are suppressed in THR (9). In our patients with THR (cases 1 and 3), suppression was observed in TSH and T4 levels subsequent to [T.sub.3] This test was not performed in our TSHoma patient (case 2), since the diagnosis had been made without a need for [T.sub.3] suppression test. None of these tests is of clear-cut diagnostic value, therefore, the use of both [T.sub.3] suppression and TRH tests are recommended, because the combination of their results increases the specifity and sensitivity of the diagnosis (8).
After TRH administration, the increase in TSH level is more than double in cases with THR, whereas it increases less than double in cases with TSHoma (1). In our patients with THR (case 1 and 3), TRH tests revealed that TSH level increased more than double. However, in our patient with TSHoma (case 2), the increase in TSH level was less than double (Table 2).
Table 2 Results of TRH stimulation tests Baseline 30 min 60 min 90 min 120 min Case 1-TSH 1.4 14.8 14.5 12.5 10.6 ([micro]IU/ml) Case 2-TSH 2.2 2.2 2.3 2.5 2.6 ([micro]IU/ml) Case 3-TSH 2.8 9.8 10.6 10.4 10.1 ([micro]IU/ml)
In TSHoma, presence of an adenoma in the pituitary gland can be detected by MRI or octreotide scintigraphy. However, since small non-functioning pituitary adenomas can be incidentally observed in 15% of normal persons, pituitary adenomas can also be incidentally observed through imaging methods in patients with THR (1).
Anti-thyroid drugs (PTU or methimazole, 200-300 mg and 20-30 mg per day, respectively) or somatostatin analogues, such as octreotide (100 mg s.c., b.i.d. or t.i.d.), along with propranolol (80-120 mg per day orally) medication may be given to the patient to restore euthyroidism before surgery (8). Tumor resection by transsphenoidal surgery alone or together with radiotherapy is the most important treatment of choice for TSHoma. Tumors are usually huge when discovered. Therefore, complete surgical resection of macroadenoma is difficult (1), (6). In the medical treatment of TSHoma, long-acting somatostatin analogues are used to control hyperthyroidism and to downsize the tumor (6), (11). Octreotid LAR 20 mg treatment led to clinical recovery in our patient with TSHoma.
In many cases with GRTH, endogenous thyroid hormones provide sufficient compensation for resistant tissues by multiplying. In these cases, there is partial resistance to thyroid hormone and as the patients are clinically euthyroid, there is no need for treatment (7), (9). Hyperthyroidism treatments such as thionamides, iodine-131 ablation treatments and thyroid surgery should be avoided in asymptomatic patients (1). Although our patient with GRTH (case 1) was asymptomatic, antithyroid drug treatment had unnecessarily been recommended just based on laboratory results. After the patient was diagnosed, follow-up was started without any treatment.
Since patients with PRTH exhibit hyperthyroid features at tissue levels, they generally require treatment to reduce the elevated thyroid hormone levels (7). In adults, treatment is basically symptomatic. Patients who are clinically hyperthyroid could benefit from [beta]-blocker and thionamides. Antithyroid drug use leads to goiter growth. The logical approach in PRTH is using agents that suppress TSH secretion. Glucocorticoides, dopaminergic drugs, somatostatin analogues, and thyroid hormone analogues can be used for this purpose. However, none of these drugs have been an ideal treatment choice due to their side effects (1), (9). 3,5,3'-Triiodothyroacetic acid (TRIAC), which is a physiological metabolite of [T.sub.3], has been found to improve endogenous thyroid hormone level, TSH, TRH or TSH response and hyperthyroidism symptoms. However, the effects of TRIAC vary and its effect on heart rate is often minimal. Additionally, some studies have failed to show that they have beneficial effects (7), (12).
We present these different three cases of inappropriate TSH syndrome to emphasize its rareness and the importance of using tests for the differential diagnosis of inappropriate TSH syndrome.
(1.) Khandwala H, Lee C. Inappropriate secretion of thyroid-stimulating hormone. CMAJ 2006;175:351-3. (2.) Florkowski CM, Brownlie BE, Croxson MS, et al. Thyroid hormone resistance: the role of mutational analysis. Intern Med J 2006;36:738-41. (3.) Nagaya T, Eberhardt NL, Jameson JL. Thyroid hormone resistance syndrome: Correlation of dominant negative activity and location of mutations. J Clin Endocrinol Metab 1993;77:982-90. (4.) Yen PM. Molecular basis of resistance to thyroid hormone. Trends Endocrinol Metab 2003;14:327-33. (5.) Ando S, Sarlis NJ, Oldfield EH, Yen PM. Somatic mutation of TR defect in negative regulation of TSH in a TSH-secreting pituitary tumor. J Clin Endocrinol Metab 2001;86:5572-6. (6.) Koriyama N, Nakazaki M, Hashiguchi H, et al. Thyrotropin-producing pituitary adenoma associated with Graves' disease. Eur J Endocrinol 2004;151:587-94. (7.) Kong AP, Lam CW, Chan AO, Yiu SF, Tiu SC. Resistance to thyroid hormone in a Chinese Family with R429Q mutation in the thyroid hormone receptor beta gene. Hong Kong Med J 2005;11:125-9. (8.) Beck-Peccoz P, Persani L, Mannavola D, Campi I. Pituitary tumours: TSHsecreting adenomas. Best Pract Res Clin Endocrinol Metab 2009;23:597-606. (9.) Refetoff S, Weiss RE, Usala SJ. The syndrome of resistance to thyroid hormone. Endocr Rev 1993;14:348-9. (10.) Takeda K, Sakurai A, De Groot LJ, Refetoff S. Recessive inheritance of thyroid hormone resistance caused by complete deletion of the protein-coding region of the thyroid hormone receptor-[beta] gene. J Clin Endocrinol Metab 1992;74:49-55. (11.) Daousi C, Foy PM, MacFarlane IA. Ablative thyroid treatment for thyrotoxicosis due to thyrotropin-producing pituitary tumours. J Neurol Neurosurg Psychiatry 2007;78:93-5. (12.) Takeda T, Suzuki S, Liu RT, Degroot LJ. Triiodothyroacetic acid has unique potential for therapy of resistance to thyroid hormone. J Clin Endocrinol Metab 1995;80:2033-4.
Hatice Sebila Dokmetas, Fatih Kilicli, Fettah Acibucu
Cumhuriyet University Medical Faculty, Department of Endocrinology and Metabolism, Sivas, Turkey
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|Title Annotation:||Case Report Olgu Sunumu|
|Author:||Dokmetas, Hatice Sebila; Kilicli, Fatih; Acibucu, Fettah|
|Publication:||Turkish Journal of Endocrinology and Metabolism|
|Date:||Dec 1, 2012|
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