Diseases of the Thyroid Flashcards

1
Q

Why does Amiodarone use decrease iodine uptake in radioiodine uptake (RAIU) scans?

A

Amiodarone is iodine-rich but also blocks peripheral deiodination of revers T3 and T4, resulting in increased reverse T3 and T4 and a decreased T3. It can cause a patient to be hyperthyroid (due to the iodine) or hypothyroid (due to too much iodine and the peripheral deiodination). Either way, RAIU is low because the thyroid is already saturated with iodine prior to the radioiodine dose.

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2
Q

Compare/contrast the radioiodine uptake scan with the thyroid scan.

A

RAIU uses radioactive iodine to measure the percentage taken up by the thyroid. The thyroid scan uses technetium to create a picture of how the isotopes localize within the thyroid. (RAIU produces a number, thyroid scan produces a picture).

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3
Q

What are the expected lab findings in a patient with acquired tertiary hypothyroidism (hypothalamus-derived)?

A

Low TSH and low or inappropriately normal free T4

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4
Q

Fill in Table 15-5 for how to interpret thyroid function tests.

A
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5
Q

What should one consider if the total T4 level is outside of the normal range?

A

First, ensure that the thyroxine-binding globulin levels are within normal limits. If TBG is outside the normal range, total T4 will be as well, and is not clinically significant.

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6
Q

What is suppurative thyroiditis and where does it most commonly occur?

A

It is a bacterial infection of the thyroid gland and typically affects the left lobe of the thyroid.

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7
Q

What factors are concerning about the presence of a solitary thyroid nodule in a child?

A

A solitary thyroid nodule in the first 20 years of life is much more likely to be malignant than in an older person, and about 26% of thyroid nodules in children are malignant.

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8
Q

What prophylactic procedure is recommended for certain mutations in MEN 2A and 2B?

A

Certain oncogenes in MEN 2A require thyroidectomy by 5 years of age and by 6 months of age with certain oncogenes in MEN 2B.

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9
Q

What happens to growth in a child with acquired hypothyroidism?

A

Growth failure is a hallmark of the disease. In most cases growth practically ceases and patients will have a weight for age that is proportionately greater than height for age.

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10
Q

Which thyroid hormone should be followed in patients with primary hypothyroidism?

A

TSH

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11
Q

If a patient with a thyroid nodule undergoes a complete thyroidectomy, what is a reliable tumor marker that should be followed to monitor for recurrence?

A

Thyroglobulin level

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12
Q

What should be the first step if an infant has a positive newborn screen for congenital hypothyroidism?

A

Send a serum TSH and free T4 to confirm the diagnosis or to diagnose congenital TBG deficiency.

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13
Q

What is the recommended treatment for myxedema coma?

A

Thyroid hormone supplementation, stress-dose glucocorticoids (until adrenal insufficiency is ruled out), and supportive care.

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14
Q

What correlates with the risk of neonatal Graves’ in a baby born to a mother with Graves disease?

A

The maternal level of TSI (TSH receptor-stimulating antibody) determines the infant’s risk for developing neonatal Graves disease as well as its’ severity. Maternal thyroid function tests have no predictive value for the infant.

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15
Q

What characterizes APS (autoimmune polyglandular syndrome) Type 2?

A

Autoimmune thyroiditis accompanied by diabetes mellitus and adrenal cortical insufficiency. It usually presents in young adults.

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16
Q

What is the most likely cause of elevated TSH in a patient on levothyroxine?

A

This value would be indicative of noncompliance until proven otherwise.

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17
Q

What symptoms should patients be instructed to go to the ED for if they are undergoing medical management for Graves disease? Why?

A

If patients develop sore throat and mouth ulcers while taking either methimazole or PTU for treatment of Graves disease they should present to the ED for evaluation of possible agranulocytosis, which requires immediate attention.

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18
Q

What disease should be considered if a patient is found to have circulating antithyroglobulin and antithyroperoxidase antibodies?

A

Most patients with Hashimoto have these antibodies circulating. However, they can also be found in people with Grave’s or in normal individuals.

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19
Q

Which endocrine disease is characterized by autoimmune thyroiditis accompanied by diabetes mellitus and adrenal cortical insufficiency?

A

APS (autoimmune polyglandular syndrome)Type 2 (AKA Schmidt syndrome)

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20
Q

What should be used to treat infants and children with congenital hypothyroidism (drug, dose, and formulation)?

A

Levothyroxine; 10-15 µg/kg/day for infants, 4 µg/kg/day for older children (100 µg/m²/day at all ages); do not give liquid formulations, as there aren’t stable liquid formulations consistently available in the U.S. market.

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21
Q

How does Graves’ present in childhood?

A

Muscle weakness, anxiety, palpitations, increased appetite, weight changes (mostly weight loss, but some have weight gain), behavior problems, declining school performance, and decreased exercise tolerance. Patients frequently have cardiac signs/symptoms (cardiomegaly, widened pulse pressure, tachycardia, HTN, and gallop rhythms). 50% of patients have a thyroid bruit on exam. Tremor, excessive perspiration, and rapid tendon reflex relaxation times are also possible. Some may have goiter. In menarcheal girls, anovulatory cycles are common and they can develop oligomenorrhea or secondary amenorrhea.

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22
Q

What are the common presenting symptoms for neonatal Graves disease?

A

Irritability, flushing, tachycardia, HTN, thyroid enlargement, and exophthalmos. Cardiac arrhythmias can occur with severe disease.

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23
Q

What symptoms are typically associated with myxedema coma?

A

Diminished mental status, hypothermia, hypotension, bradycardia, hypoglycemia, and hyponatremia.

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24
Q

Describe the clinical and laboratory presentation of neonates with congenital hypothyroidism at birth.

A

Most infants are asymptomatic at birth because of transplacental passage of maternal thyroxine (T4). However, vertical transmission of T4 provides only 33% of normal levels so neonatal screening will still reveal a high TSH and a low T4.

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25
Q

Which of T3 or T4 is the active thyroid hormone and which is the prohormone?

A

T3 is the active hormone and T4 is the prohormone.

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26
Q

What is the typical course for patients diagnosed with medullary and undifferentiated carcinomas?

A

These carcinomas have high mortality rates and require radical surgery with radiation or chemotherapy.

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27
Q

What procedure should be performed in patients with autoimmune thyroiditis who have persistent thyroid nodules despite appropriate therapy?

A

Fine needle aspiration should be performed to biopsy the prominent nodule since thyroid cancer can develop in these patients.

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28
Q

Which thyroid hormone should be followed in patients with secondary or tertiary hypothyroidism?

A

Free T4

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29
Q

What are the expected lab findings in a patient with acquired primary hypothyroidism?

A

High TSH and low free T4

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30
Q

Know the drugs and conditions that affect Thyroid function.

A
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31
Q

What are some severe (but rare) side effects of medical management for Graves disease?

A

Agranulocytosis, lupus-like syndrome, ANCA-positive vasculitis (with PTU), drug-induced fever, hepatitis, nephritis, and splenomegaly.

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32
Q

What is “thyroid storm” and how can it be prevented?

A

It’s a life-threatening hypermetabolic state which presents as tachycardia, HTN, agitation, vomiting, and diarrhea caused by a massive leakage of thyroid hormone into the circulation as a result of hyperthyroid states such as Graves disease. It can be prevented by administering β-blockers until the hyperthyroid state is controlled, and before any planned surgical interference with the thyroid in hyperthyroid individuals.

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33
Q

What laboratory tests should be performed if Graves disease is suspected?

A

TSH, free T4, free T3 should be the initial tests. Once hyperthyroidism is confirmed, TSI (TSH receptor-stimulating antibody) should be measured to confirm Graves’ as the etiology. Antithyroperoxidase and antithyroglobulin antibody levels should also be sent.

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34
Q

What are two possible complications from thyroidectomy for Graves disease?

A

Post-operative hypoparathyroidism and recurrent laryngeal nerve damage.

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35
Q

What are the expected lab findings in a patient with acquired secondary hypothyroidism (pituitary-derived)?

A

Low TSH and low or inappropriately normal free T4

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36
Q

What are the two drug options for medical management of Graves disease in children, and what is their mechanism of action?

A

Propylthiouracil (PTU) and methimazole, which both block synthesis of thyroid hormones.

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37
Q

Draw the Hypothalamic-Pituitary-Thyroid axis.

A
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38
Q

What is the typical length of treatment and efficacy of medical management for Graves disease in children?

A

Medical management typically requires 2-5 years of daily therapy and frequent physician visits. About 60-70% of patients have complete remission with medical management alone.

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39
Q

What is euthyroid sick syndrome?

A

AKA low T3 syndrome. It occurs in critically ill patients and shows low total and free T3, normal or low total T4; low, normal, or high free T4, and a normal TSH. It should resolve with treatment of the primary underlying illness.

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40
Q

What is the treatment for Graves disease?

A

β-blockers should be used to control the toxic effects of circulating thyroid hormones until the thyroid can be “turned off”. Increased production of thyroid hormones should be stopped in one of three ways: ablation of the thyroid with radioactive iodine, surgical thyroidectomy, and blocking thyroid hormone biosynthesis with drugs.

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41
Q

What is the mortality rate for neonatal Graves disease?

A

Death rates approach 25% due to high-output cardiac failure.

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42
Q

What clinical states result in a low total T4 measurement due to a decrease in thyroid binding globulin (TBG)?

A

Androgens, glucocorticoids, nephrotic syndrome, and inherited TBG deficiency.

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43
Q

Hashimoto thyroiditis occurs with increased frequency in patients with which (4) disorders?

A

Type 1 DM, Trisome 21, Turner syndrome, and Klinefelter syndrome.

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44
Q

How might an infant with congenital hypothyroidism present in the first month of life if it isn’t identified on newborn screen?

A

Before universal screening, infants would present with feeding problems, sluggishness, lack of interest, choking spells with nursing, somnolence, respiratory difficulties due to myxedema, and constipation.

45
Q

What orthopedic disorder is more common in children with hypothyroidism?

A

Slipped capital femoral epiphysis (SCFE)

46
Q

How does the presentation of suppurative thyroiditis compare with that of subacute thyroiditis?

A

Both present with fever, thyroid gland pain, and local tenderness. In suppurative thyroiditis there can be abscess formation but TFTs are normal, patients tend to be more ill-appearing, and the duration of illness is only 2-4 weeks, in contrast to 2-9 months with subacute thyroiditis.

47
Q

Which of the two options for medical management of Graves disease in children is the first-line drug, and why?

A

Methimazole is the first-line option for pediatric patients because PTU has an increased risk for hepatotoxicity and death and should therefore not be used in pediatric patients unless they cannot tolerate methimazole.

48
Q

What is the inheritance pattern in congenital thyroxine-binding globulin deficiency?

A

X-linked, so it is much more commonly seen in males.

49
Q

What condition presents with hyperthyroidism, diffuse goiter, and elevated TSH, without pituitary enlargement?

A

Selective pituitary T3 resistance

50
Q

Define Hashitoxicosis and identify the age group most commonly affected.

A

Tachycardia, nervousness, and other signs of thyroid excess with elevations in free T4 and TSH depression early in the course of the illness. This only occurs in 5-10% of patients with autoimmune thyroiditis and most commonly occurs in adolescents.

51
Q

What clinical states result in a high total T4 measurement due to a high thyroid binding globulin (TBG)?

A

Increased Estrogen from supplements, OCPs, or pregnancy; Tamoxifen, clofibrate, narcotics, hepatitis, and biliary cirrhosis.

52
Q

What is Kocher-Debre-Semelaigne syndrome?

A

Infants with congenital hypothyroidism and pseudohypertrophy.

53
Q

What fontanelle finding is helpful in diagnosing congenital hypothyroidism?

A

An enlarged posterior fontanelle should be concerning for congenital hypothyroidism, as only 3% of normal infants have an opening wider than 0.5 cm.

54
Q

What is the cause of Graves disease?

A

The body produces TSH receptor-stimulating antibodies which activate TSH receptors in the thyroid gland, causing diffuse thyroid hyperplasia and increased production of thyroid hormones.

55
Q

How often should children with Type 1 DM be screened for autoimmune thyroid disease?

A

Annually. Hashimoto occurs in about 10-15% of patients with Type 1 DM and usually presents about 5 years after the diabetes diagnosis.

56
Q

How does a radioiodine uptake scan (RAIU) scan work?

A

You give a dose of radioactive iodine and after 24 hours you place a radiation detector over the thyroid to determine the percentage of the dose taken up by the thyroid.

57
Q

What is the best time frame to screen infants for congenital hypothyroidism?

A

The ideal time for screening for congenital hypothyroidism is at about day 3. The idea is the to get the sample after the TSH surge has subsided and the T4 has risen in response.

58
Q

What are some risk factors/symptoms of thyroid cancer in children?

A

Hx of radiation to the neck/head; solitary thyroid nodule >1 cm with fixed, hard, and/or irregular borders; solitary nodule with calcifications; family hx of multiple endocrine neoplasia (MEN); rapidly growing nodule that is firm or hard; satellite lymph nodes; hoarseness or dysphagia; evidence of distant metastasis.

59
Q

Which of the three options for definitive treatment of hyperthyroidism is easiest, least costly, and most efficacious?

A

Radioactive iodine ablation of the thyroid gland.

60
Q

What bone finding in the femur helps with the diagnosis of congenital hypothyroidism?

A

The distal femoral epiphysis, which is normally present at birth, is absent in infants with congenital hypothyroidism.

61
Q

Of the solitary thyroid nodules that are shown to be cancerous, which type of cancer is most common?

A

Well-differentiated follicular carcinoma

62
Q

What is another name for Hashimoto disease?

A

Chronic autoimmune thyroiditis or chronic lymphocytic thyroiditis

63
Q

How does radioactive iodine ablation of the thyroid gland treat Graves disease?

A

It completely destroys the thyroid gland’s ability to produce thyroid hormones, which renders the patient permanently hypothyroid.

64
Q

What characterizes APS (autoimmune polyglandular syndrome) Type 1?

A

Candidiasis, hypoparathyroidism, and adrenal failure. Usually diagnosed in children 3-5 years of age and early adolescents.

65
Q

What is the recommended follow up and management for a patient with euthyroid Hashimoto disease?

A

If a patient is euthyroid but has thyroid antibodies, perform thyroid function testing every 6 months to potentially diagnose and treat a patient who has become hypothyroid.

66
Q

What test should be performed before proceeding with surgical removal of a thyroglossal duct cyst?

A

These patients should have a thyroid scan prior to surgery. If the cyst contains all of their thyroid tissue, removing it would render them hypothyroid. Families would then need to consider whether they’d prefer daily thyroid replacement therapy or periodic antibiotics with infections.

67
Q

What is selective pituitary T3 resistance?

A

Patients have hyperthyroidism with diffuse goiter and elevated TSH but no associated enlargement of the pituitary gland. This is due to a mutation which causes the pituitary gland to be resistant to the feedback of T3 on TSH.

68
Q

What condition should be suspected in a child with hyperthyroidism and an elevated/normal TSH? What other symptoms are commonly seen in this condition?

A

TSH-secreting pituitary tumor should be suspected (Thyrotropin-dependent hyperthyroidism). Patients commonly present with visual changes such as blindness or optic atrophy due to the tumor’s local manifestations. MRI should be ordered to confirm diagnosis.

69
Q

What is the most common cause of thyrotoxicosis in children and adolescents?

A

Graves disease

70
Q

What is the best method for diagnosing suppurative thyroiditis?

A

Fine needle aspiration and culture

71
Q

What is the most common cause of congenital hypothyroidism?

A

Thyroid dysgenesis (including dysgenesis, agenesis, and ectopic thyroid) is the most frequent cause of congenital hypothyroidism.

72
Q

What is the typical course for patients diagnosed with well-differentiated follicular cell carcinoma?

A

The course is usually indolent. Mortality rates are low, but nearly 1 in 3 have local or distant recurrances.

73
Q

What are common physical exam findings in infants with symptomatic congenital hypothyroidism?

A

Infants have short extremities with widened fontanelles, abdominal distention with umbilical hernia, hypotonia, delayed dentition, macroglossia due to myxedema, and jaundice due to hyperbilirubinemia.

74
Q

What are some possible abnormalities in patients with congenital hypothyroidism that can occur despite appropriate therapy?

A

About 20% of patients have neurosensory hearing defecits, and there is an increased risk for other congenital malformations such as kidney defects and cardiovascular anomalies.

75
Q

How does subacute thyroiditis present?

A

Fever with pain and tenderness of the thyroid gland. Initially there are signs and symptoms of hyperthyroidism, followed by a more prolonged period of hypothyroidism.

76
Q

What is the therapy for subacute thyroiditis?

A

Symptoms can usually be controlled with analgesics, or rarely with severe disease, prednisone. Generally the illness lasts 2-9 months with no residual defect in thyroid function.

77
Q

What is the most common cause of acquired hypothyroidism in the U.S.?

A

Autoimmune thyroiditis

78
Q

What usually precipitates subacute thyroiditis?

A

Upper respiratory infections.

79
Q

What hormone does medullary carcinoma of the thyroid produce? What cells produce it?

A

Calcitonin, which is produced by the parafollicular cells of the thyroid gland (AKA C-cells).

80
Q

What mutations are responsible for MEN 2A and 2B?

A

MEN 2A and 2B are caused by activating mutations of the RET oncogene.

81
Q

What are the two treatment goals for management of Graves disease?

A

Blunting the toxic effects of circulating T3/T4 and stopping further increased production of T3/T4.

82
Q

How do you treat a patient with euthyroid sick syndrome?

A

Treat the primary underlying illness, as this is a non-thyroidal illness and does not require thyroid replacement therapy.

83
Q

Which endocrine disease is characterized by candidiasis, hypoparathyroidism, and adrenal failure?

A

APS (autoimmune polyglandular syndrome)Type 1 (AKA autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy or Whitaker syndrome)

84
Q

What is the most common cause of goiter in children >6 years of age in the U.S.?

A

Hashimoto thyroiditis (AKA chronic autoimmune thyroiditis)

85
Q

What are the typical lab findings in infants with neonatal Graves disease?

A

Elevated total and free T4, T3, and TSI with low TSH.

86
Q

Create a decision tree for the recommended evaluation of a pediatric thyroid nodule. ***

A

***, see page 15-25

87
Q

Which pathogens are most commonly responsible for suppurative thyroiditis?

A

S. aureus, S. pyogenes, and S. pneumoniae

88
Q

What is neonatal Graves disease and what maternal factors should make one consider the diagnosis?

A

Neonatal Graves disease is neonatal hyperthyroidism due to transplacental transmission of maternal TSI (TSH receptor-stimulating antibody). Any maternal history of Graves disease (even after definitive treatment) should make one consider neonatal Graves disease because the TSI may never go away.

89
Q

What is the most common side effect from PTU and methimazole? What is the most serious side effect?

A

Skin rash is the most common side effect from use of these drugs. Granulocytopenia is the most serious side effect.

90
Q

In which patients is radioactive iodine ablation of the thyroid gland the recommended treatment modality?

A

In patients >10 years of age who have had poor response to antithyroid drugs. (Some specialists are using it as the preferred initial therapy)

91
Q

What are the two most important thyroid function tests?

A

TSH (most sensitive indirect test of thyroid function) and Free T4 (which is the metabolically active thyroid hormone).

92
Q

In what situations would radioiodine uptake scanning be helpful? In what situations would it be useless?

A

Radioiodine uptake scanning can be helpful in differentiating between nonpituitary thyrotoxic states (i.e. low TSH w/ high free T4). It is not useful in diagnosing causes of hypothyroidism.

93
Q

List several (7) causes of acquired hypothyroidism.

A

Autoimmune thyroiditis, drugs, natural goitrogens, thyroid dysgenesis, acquired hypothalamic or pituitary problems, iodine deficiency, and thyroglossal duct excision.

94
Q

Radioiodine uptake (RAIU) is low in which disorders?

A

It is low in self-limited thyroiditis-induced thyrotoxic states (painless chronic thyroiditis, postpartum thyroiditis, subacute thyroiditis, and the hyperthyroid phase of Hashimoto’s), thyroiditis factitia, and with amiodarone use.

95
Q

What is subacute thyroiditis?

A

It is a self-limited inflammation of the thyroid, typically following a URI.

96
Q

How are most infants with congenital hypothyroidism identified?

A

Most are now identified on the newborn screen.

97
Q

In what clinical situation would you use a thyroid scan as part of the diagnostic workup?

A

The thyroid scan is only used for nodular disease in order to determine whether a nodule is hot (functioning) vs cold (nonfunctioning).

98
Q

What is a commonly tested x-ray finding for infants with congenital hypothyroidism?

A

X-ray of the skull would reveal large sutures.

99
Q

Why is the timely diagnosis of congenital hypothyroidism so important?

A

Developmental delay and permanent loss of IQ occurs before clinical symptoms are evident, and affected infants <3 years of age lose IQ points for every week they are not treated.

100
Q

What lab studies should be performed if myxedema coma is suspected?

A

TSH, free T4, and cortisol levels to rule out coexisting adrenal insufficiency.

101
Q

What imaging study should be performed if you are concerned for secondary or tertiary hypothyroidism?

A

Brain MRI to rule out any hypothalamic-pituitary axis pathology as the etiology for the hypothyroidism.

102
Q

What diagnosis should one consider if a patient presents with a centrally located neck mass that moves with swallowing?

A

Thyroglossal duct cyst.

103
Q

Name the things thyroxine tablets will bind to and should not be co-administered with.

A

Soy protein formula, calcium supplements, and iron.

104
Q

Radioiodine uptake (RAIU) is high in which disorders?

A

Graves disease and hot nodules (e.g. multinodular goiter, toxic solitary nodule, hCG-secreting tumor).

105
Q

What is myxedema coma?

A

It is a rare medical emergency characterized by severe hypothyroidism leading to the slowing of multiple organ systems.

106
Q

What is the most definitive test that can be performed to determine the cause of a patient’s thyroid nodule?

A

Fine needle aspiration

107
Q

What would be the typical clinical and laboratory findings in infants with congenital TBG deficiency?

A

Free T4 and TSH should be normal, with a low total T4. They are clinically euthyroid and do not require any intervention.

108
Q

What is the normal physiology of thyroid hormones in a neonate after birth?

A

There is a surge ot TSH that peaks by 12 hours of age. This is followed by a rise in T3 and T4 levels, which peak during the first day of life and then slowly fall.