Endo Flashcards
A 45-year-old female had myalgias, a sore throat, and a fever 2 weeks ago. She now has anterior neck tenderness and swelling, with pain radiating up to her ears. Your examination reveals a tender goiter.
Which one of the following would support a diagnosis of subacute granulomatous thyroiditis? (check one)
Pretibial myxedema
Exophthalmos
Multiple nodules on ultrasonography
Low radioactive iodine uptake (<5%)
Low radioactive iodine uptake (<5%)
Subacute granulomatous thyroiditis is the most common cause of thyroid pain. Free T4 is elevated early in the disease, as it is in Graves disease; however, later in the disease T4 becomes depressed and then returns to normal as the disease resolves. Pretibial myxedema, exophthalmos, and a thyroid thrill or bruit can all be found in Graves disease, but are not associated with subacute granulomatous thyroiditis. Multiple nodules on ultrasonography suggests multinodular goiter rather than subacute granulomatous thyroiditis. Patients with subacute granulomatous thyroiditis will have a low radioactive iodine uptake (RAIU) at 24 hours, but patients with Graves disease will have an elevated RAIU (SOR C).
A 45-year-old female is being treated for hypothyroidism with levothyroxine (Synthroid), 112 :g daily. She is still having persistent fatigue and weight gain despite her TSH value of 1.5 :U/mL (N 0.5–5.5).
In addition to evaluating this patient for other causes of her symptoms, which one of the following would be appropriate management of her thyroid medication at this time? (check one)
Continuing the current therapy
Increasing the dosage
Adding liothyronine (Cytomel)
Switching to desiccated thyroid hormone (Armour Thyroid)
Continuing the current therapy
Some hypothyroid patients who are treated with appropriate dosages of levothyroxine and whose TSH levels are in the appropriate range continue to have persistent symptoms such as fatigue, depressed mood, and weight gain. If the TSH is in the appropriate range then no adjustment is necessary and annual serum TSH testing is recommended. Patients who remain symptomatic on an appropriate dosage of levothyroxine, as determined by a TSH <2.5 mIU/L, are not likely to benefit from combination triiodothyronine/thyroxine therapy (SOR A). Desiccated thyroid hormone preparations are not recommended by the American Association of Clinical Endocrinologists for the treatment of hypothyroidism. A meta-analysis of 11 randomized, controlled trials of combination T3/T4 therapy versus T4 monotherapy showed no improvements in pain, depression, or quality of life (SOR A).
A previously healthy 58-year-old female sees you for evaluation of increased hair growth on her face and a weight gain of 18 kg (40 lb) over the past year. An examination is significant for a blood pressure of 155/98 mm Hg, a BMI of 34 kg/m2 with a truncal obesity pattern, striae on the sides of the torso and lower abdomen, marked hirsutism, and a rounded, swollen facial appearance. A urine pregnancy test is negative. Liver and renal function tests are normal, as are TSH, electrolyte, testosterone, and DHEA levels. A hemoglobin A1c is 6.2%.
Which one of the following would be most useful to diagnose the condition suggested by this patient’s presentation? (check one)
A 24-hour urinary free cortisol level
24-hour urinary metanephrines
ACTH stimulation testing
FSH and LH levels
Plasma renin activity testing and an aldosterone level
A 24-hour urinary free cortisol level
This patient presents with clinical findings strongly suggestive of Cushing disease, which is defined as the excessive production of adrenal cortical hormones. Options for confirmatory testing include 24-hour urinary free cortisol and overnight salivary cortisol levels. Metanephrines are used to diagnose pheochromocytoma. ACTH stimulation testing is used to diagnose adrenal insufficiency. FSH and LH levels test the hypothalamic-pituitary-gonadal axis. Plasma renin activity testing and an aldosterone level are useful in the workup of secondary hypertension to help diagnose hyperaldosteronism.
Pretibial myxedema is a cutaneous manifestation of?
(check one)
Subclinical diabetes mellitus
Collagen vascular disease
Hyperlipidemia, type III
Ischemia
Graves disease
Graves disease
Pretibial myxedema is a complication of Graves disease, whether it presents as hypo-or hyperthyroidism. It is a dermopathy that most often occurs in the lower legs and results from increased deposition of mucin due to the endocrine abnormality. Diabetes mellitus can cause necrobiosis lipoidica, a lesion on the lower extremities; hyperlipidemia can cause waxy papules; and collagen vascular and ischemic disease can cause urticaria and/or ulceration.
A 47-year-old postmenopausal female falls while carrying groceries into her house and sustains a right distal radial fracture. A chemistry panel reveals a calcium level of 11.2 mg/dL (N 8.6–10.6) and further evaluation leads to a diagnosis of primary hyperparathyroidism.
Which one of the following is the best course of treatment for this patient?
(check one)
Estrogen replacement therapy
Long-term bisphosphonate therapy
Daily furosemide treatment with increased oral fluids
Elimination of calcium and vitamin D from the diet
Referral to a surgeon for consideration of parathyroidectomy
Referral to a surgeon for consideration of parathyroidectomy
Hyperparathyroidism is usually caused by a single adenoma of one of the four parathyroid glands. A minority of cases (10%–15%) are associated with four-gland hyperplasia. Studies that localize the glands, such as a technetium scan or ultrasonography, help surgeons who are familiar with this condition achieve a cure rate of 95%–98%, with an estimated complication rate of 1%–3%. For patients <50 years old or symptomatic patients, such as those with a fragility fracture, parathyroidectomy is the treatment of choice. If a patient is older, is a poor surgical candidate, or has asymptomatic disease, long-term monitoring with treatment focused on reducing bony complications can be considered (SOR C).
A 35-year-old nulligravida sees you for preconception counseling. She has hypothyroidism treated with levothyroxine (Synthroid), and her most recent TSH level was in the therapeutic range. She has no symptoms of hypothyroidism.
Which one of the following is the patient most likely to require if she becomes pregnant? (check one)
A decreased dosage of levothyroxine
An increased dosage of levothyroxine
The addition of liothyronine (Cytomel)
Substitution of desiccated thyroid hormone preparation (Armour Thyroid) for the levothyroxine
An increased dosage of levothyroxine
Thyroid hormone requirements increase during pregnancy. Most women with hypothyroidism who become pregnant require an increased levothyroxine dosage (SOR A). A common recommendation is to have women on fixed daily doses of levothyroxine begin taking nine doses weekly (one extra dose on 2 days of the week) as soon as the pregnancy is confirmed (SOR B). Thyroid function tests should be repeated regularly throughout the pregnancy to guide additional dosage adjustments.
A patient with ascites is suspected to have secondary hyperaldosteronism. Which one of the following would be typical levels of electrolytes in an aliquot specimen of urine? (check one)
Sodium 2 mEq/L, potassium 40 mEq/L
Sodium 5 mEq/L, potassium 0 mEq/L
Sodium 40 mEq/L, potassium 40 mEq/L
Sodium 80 mEq/L, potassium 2 mEq/L
Sodium 100 mEq/L, potassium 20 mEq/L
Sodium 2 mEq/L, potassium 40 mEq/L
Secondary hyperaldosteronism is characterized by sodium retention, and thus decreased urinary sodium excretion, while potassium secretion is normal to increased.
A 21-year-old gravida 1 para 0 is diagnosed with overt hyperthyroidism early in the first trimester. The most appropriate management at this time is (check one)
observation only
methimazole (Tapazole)
propylthiouracil
radioactive iodine
thyroidectomy
propylthiouracil
Overt hyperthyroidism during pregnancy is associated with adverse effects to the mother and fetus, so treatment is required. Since methimazole is associated with birth defects when used in the first trimester, propylthiouracil is preferred. Methimazole should be considered after the first trimester because the risk of congenital anomalies is less than the risk of liver failure associated with propylthiouracil. Surgery and radioactive iodine should only be used if there is a clear indication, and radioactive iodine would not be appropriate during pregnancy.
In a 27-year-old white female with irregular menstrual cycles and infertility, which one of the following would be more indicative of Cushing’s syndrome rather than the more common polycystic ovarian syndrome? (check one)
Easy bruising
Acne
Hirsutism
Androgenic alopecia
Acanthosis nigricans
Easy bruising
Easy bruising, moon facies, buffalo hump, abdominal striae, hypertension, and proximal myopathy suggest Cushing’s syndrome. Because this syndrome is very rare compared to polycystic ovarian syndrome, routine screening is not indicated in women with hypoandrogenic anovulation. Acne, hirsutism, androgenic alopecia, and acanthosis nigricans are all consistent with polycystic ovarian syndrome.
A 60-year-old female comes to your office several weeks after an emergency department (ED) visit for ureteral colic. At that time, a comprehensive metabolic panel was normal except for a calcium level of 10.6 mg/dL (N 8.6–10.5). An ionized calcium level was also elevated. A urinalysis showed 20 RBCs/hpf but a urine culture was negative. CT of the abdomen and pelvis demonstrated a 4-mm radiopaque calculus in the distal ureter but no other abnormality. She was treated with analgesics and tamsulosin (Flomax) and passed the stone several days later.
She currently has no urinary or gastrointestinal symptoms. This is her third episode of ureterolithiasis in the past 5 years.
Which one of the following would be the most appropriate test to order next? (check one)
An intact parathyroid hormone level
A 24-hour urine sample for calcium
A TSH level
Repeat urinalysis and urine culture
Renal ultrasonography
An intact parathyroid hormone level
Hyperparathyroidism is an under-recognized cause of recurrent nephrolithiasis. Mild elevations of serum calcium levels are often overlooked or ignored. Surgical treatment of hyperparathyroidism can reduce serum calcium levels, hypercalciuria, and the formation of kidney stones.
A 24-hour urine sample for calcium would not be the most appropriate next step. Thyroid disorders are not directly linked to nephrolithiasis so a TSH level is not indicated. Repeat urine studies will not affect management. A CT scan in the emergency department was sufficient to rule out anatomic abnormality, so renal ultrasonography is not necessary.
A 45-year-old female presents with a 1-week history of pain at the base of her anterior neck radiating to her right jaw. Prior to the onset of pain she had a sore throat, fever, and body aches. These symptoms resolved and the neck pain started. She now reports palpitations and excessive sweating.
Her vital signs include a pulse rate of 110 beats/min, a blood pressure of 140/83 mm Hg, and a normal temperature. On examination she appears uncomfortable and diaphoretic. An HEENT examination is unremarkable and you note no cervical lymphadenopathy. Her thyroid is tender and mildly enlarged. A cardiac examination shows tachycardia with no murmurs.
Laboratory studies reveal a normal CBC, an erythrocyte sedimentation rate of 55 mm/hr (N 0–29), and a TSH level of 0.21 μU/mL (N 0.5–5.0). Total T3 and free T4 levels are within the normal range. You order a radioactive iodine uptake scan, which shows diffusely low iodine uptake in her thyroid.
In addition to a β-blocker, which one of the following would be most appropriate at this point? (check one)
Ibuprofen, 800 mg three times daily
Levothyroxine (Synthroid), 50 μg daily
Methimazole, 5 mg three times daily
Prednisone, 40 mg daily
Vancomycin, 20 mg/kg intravenously every 12 hours
Ibuprofen, 800 mg three times daily
This patient has signs and symptoms consistent with subacute thyroiditis, which is confirmed by laboratory testing (an elevated erythrocyte sedimentation rate, a low TSH level, and normal T3 and T4 levels) and a radioactive iodine uptake scan with diffusely low iodine uptake. Subacute thyroiditis often follows a viral infection and is most common in women in their fifties, with peak occurrence in the late summer and fall months. The goal of treatment is to reduce thyroid pain and treat symptoms of thyrotoxicosis. High-dose NSAIDs or acetylsalicylic acid are first-line recommendations (SOR C). This patient would also benefit from the use of a β-blocker to ameliorate her tachycardia and diaphoresis.
During the acute thyroiditis phase, thyroid hormone supplementation is not indicated and will likely worsen symptoms. Levothyroxine would be indicated once the acute thyrotoxic phase resolves and there is evidence of hypothyroidism. Since subacute thyroiditis is a self-limited condition, levothyroxine is recommended for 12 months. Antithyroid medications such as methimazole are not indicated in subacute thyroiditis, which is a destructive process itself. While glucocorticoids such as prednisone provide faster pain relief than first-line NSAIDs or aspirin, they should not be used unless first-line treatments have failed to resolve symptoms in 4 days. Antibiotics are prescribed in suppurative thyroiditis, which is characterized by fever, leukocytosis, and cervical lymphadenopathy in addition to thyroid pain. They should be started empirically after negative blood cultures have been obtained.
A 12-year-old transgender female accompanied by her mother comes to your office to discuss persistent gender dysphoria. The patient has been in counseling for 2 years along with her family, who is supportive of her gender identity. The patient’s mother asks about puberty blockers.
In discussing GnRH analogs with her, you note that the current recommendation for beginning this medication is when she is at which Tanner stage of development? (check one)
1
2
3
4
5
2
The 2022 World Professional Association for Transgender Healthcare (WPATH) standards of care recommends that in eligible adolescents, pubertal suppression may begin at Tanner stage 2. Treatment prior to the onset of puberty is not recommended. Tanner stage 1 is prepubescent and Tanner stage 2 is the initial pubescent stage. It is not necessary and may be harmful to wait for further pubertal stages before initiating puberty blockers in an eligible transgender adolescent.
A 45-year-old female sees you for follow-up 3 days after a visit to the emergency department (ED) for acute abdominal pain due to an initial episode of a kidney stone. Her past medical history and family history are unremarkable. A CT scan in the ED demonstrated a nonobstructing, 4-mm mid-ureteral stone and several smaller stones in both kidneys, measuring up to 2 mm. Laboratory studies in the ED showed a calcium level of 11.4 mg/dL (N 8.0–10.0) and microscopic hematuria on urinalysis but were otherwise normal. She was treated with intravenous hydration and pain control and was discharged home. She passed the stone the next day.
A physical examination today is normal. Follow-up laboratory studies confirm an elevated serum calcium level, along with elevated serum parathyroid hormone and 24-hour urine calcium levels. A DEXA scan and repeat microscopic urinalysis are normal.
At this point, you should (check one)
prescribe a bisphosphonate
prescribe a thiazide diuretic
refer her for genetic evaluation
refer her for cystoscopy
refer her for parathyroidectomy
refer her for parathyroidectomy
This patient has laboratory evidence of primary hyperparathyroidism, with hypercalcemia and an inappropriately elevated (as opposed to suppressed) parathyroid hormone (PTH) level. An elevated 24-hour urine calcium level further distinguishes primary hyperparathyroidism from familial hypocalciuric hypercalcemia. Treatment of primary hyperparathyroidism with parathyroidectomy has been shown to normalize PTH and calcium levels, decrease kidney stone production, and prevent declines in renal function and bone mineral density. Untreated primary hyperparathyroidism increases overall mortality as well as cardiovascular and cerebrovascular disease risk, in addition to increasing the risk of kidney stone production, renal function decline, and loss of bone mineral density. Parathyroidectomy is indicated in this patient based on her symptomatic hypercalcemia, age <50, and serum calcium level >1 mg/dL above the upper limit of normal. Other potential indications include the presence of osteoporosis, reduced kidney function, or other asymptomatic renal involvement, including silent nephrolithiasis on imaging, nephrocalcinosis, or hypercalciuria.
Patients with primary hyperparathyroidism who are not candidates for surgery may be managed medically. Bisphosphonates may be used to increase bone mineral density. For this patient with a normal DEXA scan, surgical treatment would obviate the possible future need to treat her for bone density loss related to hyperparathyroidism. Thiazides may be used for treating certain hyperparathyroid states due to their impact on reducing calcium excretion and improving bone mineral density, although they are typically avoided in primary hyperparathyroidism because they can worsen hypercalcemia. Genetic evaluation would be warranted for a patient suspected of having multiple endocrine neoplasia type 1 or 2A, although this patient does not have any family history or presenting features to suggest involvement of either of these rare familial syndromes. Cystoscopy may be indicated in the setting of ureteral obstruction but is not necessary in this case.
The most common electrolyte abnormality in a patient with primary hyperaldosteronism is (check one)
hypocalcemia
hypokalemia
hyponatremia
hyperkalemia
hypernatremia
hypokalemia
Primary hyperaldosteronism was previously thought to be rare, but it is now considered one of the more common causes of secondary hypertension. Hypokalemia is the most common electrolyte abnormality in patients with hyperaldosteronism. Excess aldosterone secretion independent of the renin-angiotensin system causes renal potassium wasting, although about half of patients with hyperaldosteronism have normal potassium levels. Hypocalcemia is commonly associated with inadequate levels of parathyroid hormone. Hyponatremia and hyperkalemia are associated with primary hypoaldosteronism. Hypernatremia is not a common finding in primary hyperaldosteronism.
Which one of the following is known to cause hyperthyroidism? (check one)
Propranolol (Inderal)
Amiodarone (Cordarone)
Methimazole (Tapazole)
Propylthiouracil
Methotrexate (Rheumatrex, Trexall)
Amiodarone (Cordarone)
Amiodarone is 37% iodine and is the most common source of iodine excess in the United States.
Excessive iodine intake from dietary sources, radiographic contrast media, or amiodarone increases the
production and release of thyroid hormone in iodine-deficient individuals and in older persons with
multinodular goiter. Additionally, like other medications such as interferon and interleukin-2, amiodarone
can trigger thyroiditis in patients with normal thyroid glands. These characteristics combine to induce
hyperthyroidism in slightly over 10% of patients treated with amiodarone. -Blockers such as propranolol may be useful in controlling the symptoms of hyperthyroidism. Methimazole and propylthiouracil interfere with organification of iodine, thereby suppressing thyroid hormone production; they are commonly used as antithyroid agents when treating hyperthyroidism. Research is ongoing to determine if methotrexate plus prednisone is an effective treatment for the ophthalmopathy associated with Graves’ hyperthyroidism.