endocrinology Flashcards

1
Q

Hyperthyroidism
etiology
primary (dec TSH)

A

Graves disease (antibody against TSH receptor)
Plummers disease: Multinodular toxic goiter. Hyperfuctioning areas that produce high T3 and T4 –> dec TSH –> atrophy of rest. Have + anti peroxidase and anti thyroglobulin antibodies
subacute thyroiditis

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2
Q

Hyperthyroidism
etiology
secondary (inc TSH)

A

pititary adenoma, hypothalamic disease, germ cell tumor, strauma ovarii, metastatic follicular thyroid carcinoma

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3
Q

Clinical of hyperthyroidism

A

Heat intolerance, tachycardia, sweating, weight loss despite inc appatite. hand tremor, hyperactivity, nervousness, insomia, irritability, diarrhea, palpitation, muscle weakness.
exopthalmos, arrhythmia, increased BP, pretibial myxedema:

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4
Q

hyperthyroidism diagnosis

A

dec if primary, inc if secondary, TSH, T3, T4. Radioactive T3 uptake, scintiography = diffuse uptake in graves and patchy in multinodular toxic (plummer disease)

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5
Q

Treatment

A

Methimazole (contraindicated in pregnancy), and propylthiouracil. (inhibit thyroid hormone synthesis). B-blocker, Radioiodine 131.

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6
Q

special symptoms for graves disease

A

Goiter, bruits, exophtalmos, pertibial myxedema.

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7
Q

what is thyroid storm

A

life-threatening complication of hypert characterized by fever, tachycardia, agitation, psychosis, confusion, NVD. precipitated by infections, DKA, stress: birth, trauma, surgery. Treated with ptu + iodine, b-blocker, dexamethasone (inhibits T3–> T4)

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8
Q

Painful tender thyroid gland

A

Subacute thyroiditis. usually follow a viral ille ness –> hypert –> eu –> hypot. Low radioiodine uptake. t: NSAIDS + aspirin +- corticosteroids.

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9
Q

Hypothyroidism

A

Primary: failure of gland to produce hormone: Hashimoto´s disease (MC, antimicrosomal ab), iatrogenic: prior tx of hyperthyroidism:radioiodine, thyroidectomy, medications.
Secondary: pituitary (low TSH) or hypothalamic (low TRH)

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10
Q

Clinical feature of hypothyroidism:

A

fatigue, weakness, lethargy, weight gain, cold intolerance, CONSTIPATION, depression, muscle weakness. goiter, bradycardia, carpal tunnel syndrome, coarse hair, hoarsness, nonpitting edema.

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11
Q

Diagnosis of hypthyroidism

A

High TSH if primary, or low TSH if secondary or tertiary. Low free T4. Hashimoto: inc antimicrosomal an. inc LDL

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12
Q

Tx of hypothyroidism

A

Levoxine. effect is evident 2-4 w, one daily, monitor TSH levels.

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13
Q

Subclinical hypothyroidism

A

inc TSH and T4 is normal. mild symptoms of hypothyroidism. look for elevated LDL!!!

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14
Q

TPO and TG antibody found in which disease

A

Hashimoto

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15
Q

Addisons disease: ethiopathogenesis,

A

Addisons = primary adrenal insufficency. Causes: autoimmune, infectious (TB), iatrogenic (bilateral adrenalectmy), metastatic (breast, lung)

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16
Q

Addisons disease

clinical

A

GI symp, mental symptoms, hypoglycemia, hyperpigemntation, low aldosterone leading to hyponatremia and hyperkalemia.

17
Q

Addisons disease

Dx

A

decreased cortisol level, lack of response to infusion wit synthetic ACTH. MRI of brain to rule out hyperparathyroidism.

18
Q

Tx of Addisons disease

A

daily oral glucocorticoid and mineralocorticoid

19
Q

Thyroid cancer ssx

A

suggested if nodue is fixed in place and no movement on swallowing. firm consistancy and irregularity, solitary, Hx of radiation to neck, vocal cord paralysis, cervical adenopathy, FH or elevated serum calcitonin

20
Q

Dx and types of thyroid cancer

A

USG guided FNA Thyroid scan (cold nodule)

Types: papillary (radiation), follicular, medullary (produce calcitonin), anaplastic.

21
Q

Pheochromocytoma: clinical picture, dx ddx tx

Def

A

Pheochromocytoma: Tumors that produce, store and secrete cathecholamine. Arise from chromaffins cell of the adrenal medulla (90%) and or symp ganglia.

22
Q

Pheochromocytoma clinical

A

HTN, punding headache, sweating, tachycardia, palpitation, anxiety

23
Q

Pheochromocytoma dx

A

LAB: hyperglycemia, hyperlipidemia, hypokalemia, Urine: metanephrine, vanillylmadelic acid

24
Q

Type 1 diabetes mellitus: def

A

is an autoimmune disease, that destroyd B cells of pancreas. This is characterized by severe deficiency of insulin. Onset i typically before 20 yrs, but can occur at an age. Type 1 DM is not related to obesity. Only 5 % of diabetic patients

25
Q

Type 1 diabetes mellitus: diagnosis

A

Two fasting glucose measurements > 126 mg/dl. Single glucose level of 200 mg/dl with symptoms, Increased glucose levels on oral glucose tolerance testing. HbA1c >6,5 %

26
Q

Ss of DM1

A

symptoms develop quickly over days to weeks, can occur after an illness. And is often presented as acute DKA

27
Q

SS DM2 (and 1?)

A

polyuria, polydipsia, fatigue, weight loss, blurred vision, fungal infections. Numbness, tingling of hands and feet.

28
Q

Treatment of DM1

A

Insulin, adjust dose according to glucose levels. Intensive insulin therapy: long-acting insulin is given once daily in the evening. then regular (fast and short acting) insulin is given 30 min before each meal.

29
Q

Treatment of DM2

A

Diet, exercise, oral hypoglycemics (usually metformin) start on one drug than add one more from another group if monotherapy fails. Then insulin as last treatment option.

30
Q

DM 2 def:

A

Ranges from predominantly insulin resistance with relative insulin deficiency to a predominantly insulin secretory defect with insulin resistance secondary to b cell dysfunction. Insulin levels normal to high in the beginning, then diminish over many years of having diabetes.

31
Q

DM2 ethiopatho

A

obesity is associated with increased plasma level of free fatty acid, which make muscles more insulin resistant, reducing glucose uptake. Therefore, obesity exacerbates insulin resistance.

32
Q

Screening for diabetes type 2

A

adults over 45 yrs evert 3 years. For those w risk factors: obesity, FHx, Hx of gastational DM. start earlier.

33
Q

Complications of diabetes:

A

Macrovascular complications: CAD (accelerated rate of atherosclerosis) Peripheral vascular disease. Stroke (cerebrovascular disease)
Microvascular:
Diabetic nephropathy: = most important cause of ESRD. Proteinuria + HTN
Retinopathy, catarac, galucoma. (annulally screening is recommended) Edema of macula is the leading cause of blindness. Distal symmetrical neuropathy.

34
Q

Screening for diabetic nephropathy

A

MICROALBUMINURIA!!. takes 1-5 yrs before developing proteinuria. Tx: ACEI for BP control.

35
Q

DKA

A

hyperglycemia, ketosis, and met acidosis.