Endo Flashcards

1
Q

30% of all pituitary adenomas

Females = Amenorrhea, galactorrhea, infertility
Males = vague sxs (decreased libido)

What is it? Tx?

A

Lactotropic adenoma (prolactinoma)

Tx = Bromocriptine (surgery for large tumors/failed pharm)

(smaller than 10mm = microadenoma)

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2
Q

Somatotropic adenoma (growth hormone)… Has two different presentations based off puberty. what are they?

Tx = surgical excision, BONE CHANGES ARE PERMANENT

A

pre puberty = Gigantism (growth of long bones = ~8ft tall)

Post puberty = acromegaly (growth of hands/feet/face/jaw)

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3
Q

Complication of post puberty somatotropic adenomas?

A

Internal organ enlargemetn… cardoresp comps may cause death

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4
Q

Cushing from over stimulation of adnreal cortex results from?

A

Corticotropic adenoma (ACTH)

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5
Q

Causes of hypopituitarism?

which is rare, btw

A

Congenital (primary empty sella syndrome, dwarfism, hypogonadism)

Tumors (decreases circulation/destroys pituitary gland)

Circulatory disturabances (Sheehan’s syndrome)

Trauma (head injury/trauma)

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6
Q

Postpartum ischemia

Massive hemorrhage/HOTN from childbirth

(Similar process to acute renal tubule necrosis)

A

Sheehan syndrome

can cause hypopituitarism

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7
Q

COLD INTOLERANCE

HOTN

General weakness

Poor appetite

A

SSx of hypopituitarism

Cold intolerance/HOTN being the key dffierentiator

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8
Q

Damage to hypothalamus, pituitary stalk, tumors, trauma

-> insufficient ADH

Ssx?

A

Diabetes inspidus

Polyuria
Polydipsia
BUT NO polyphagia

(Water restriction does not affect urine output)

Tx = vasopressin

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9
Q

Most common cause of hyperthyroidism?

Clinical features/

A

Graves Dz (autoimmune)

Ssx appear slowly

Restlessness/nervousness
Tremors/excessive sweating
Heart palpitation
*High t3/t4
*LOW TSH

Tx = I131, surgical excision

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10
Q

Typical Graves dz pt?

Characterized by?

A

20-40 y/o woman

Thyrotoxicosis
Exophthalmos
Dermopathy - pretibial myxedema - dough like skin that doesn’t pit (<4%)

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11
Q

Most common hypothyroidism

A

Hashimoto’s

Autimmune dz associated with other dz (Sjogrens)

Females are 10x more likely

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12
Q

Other less common forms of hypothyroidism

A

Thyroidectomy

Iodine deficiency (rare… cretinism/goiter)

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13
Q

Features of hypothyroidism

A

SLOWING OF ALL METABOLIC PROCESSES

Low T3/T4 (HIGH TSH)

Sleepiness/cold sensitivity/constipation/ wt gain

TX = synthetic thyroid supps

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14
Q

Iodine deficiency presents with?

Must r/o cancer when seeing this sign

A

Nodular goiter

Hypothyroid symptoms

Normal to low thyroid hormones (HIGH TSH)

Tx = incomplete thyroidectomy

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15
Q

Common benign tumor usually presenting as solitary nodule

Can’t be differentiated from normal tissue on I123 scan
Diagnosis by biopsy

A

Follicular adenoma

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16
Q

Most common malignant thyroid nodule

Inactive

Does not take up I123 on scan (“cold nodule”)

Biopsy -> partial/total thyroidectomy

A

Papillary thyroid carcinoma

17
Q

15% of malignant thyroid tumors

Hot nodule (seen on I123 scan)

Susceptible to I131 ablation

A

Follicular thyroid carcinoma

18
Q

Increased secretion of PTH

Most commonly from?

A

Hyperparathyrdiism usually from benign parathyroid adenoma

(usually asymptomatic; however severe cases may lead to pathological fxs of bones/kidney stone formation)

Labs = high Ca, low PO

19
Q

Labs = low Ca, high PO

Muscle spasms/cramps

Chvostek’s sign (facial twitching from tapping)

Trousseau’s sign (wrist flex from BP cuff)

A

Hypoparathyroidism (rare)

20
Q

Hypercortisolism?

Causes?

A

Cushing’s
1. Pituitary adenoma = too much ACTH Cushing’s Dz (MC)

  1. Adrenocortical tumor = too much corticosteroids = Cushing’s syndrome
  2. Exogenous glucocorticoids = Prolonged tx of autoimmune d/o
21
Q

Central truncal obesity

Moon faces

BUffalo hump

Facial redness

Cutaneous striae

Facial hair/thinning/acne

A

Cushings

22
Q

Tx for Cushing’s?

A

Excision of tumor

Medical suppression of endocrine system

OR if due to exogenous steroids, taper/cease steroids

23
Q

Chronic adrenocortical inufficiency

A

Addison’s dz

Progressive destruction of adrenal cortex

24
Q

Slow insidious onset

Progressive weakness/fatigue

BRONZING hyperpigmentation (stimulated melanocytes)

A

Addison’s

Tx = life long corticosteroid supplements

25
Q

ACTH test administration should trigger corticosteroid release…
If no response, suspect?

A

Addison’s

26
Q

Catecholamine secretion tumor

Rare neoplasm of adrenal medulla

Strong familial association w/ MEN (multiple endocrine neoplasia)

A

Pheochromocytoma

27
Q

Classic triad =

HA
Diaphoresis
Tachycardia

A

Pheochromocytoma

ABRUPT onset of HTN

28
Q

Many people w/ pheochromocytoma don’t have classic triad. Other ssx?

A

Tachycardia, palpitations, tremor, apprehension

29
Q

What labs will be elevated in pheochromocytoma?

A

Epi/norepinephrine elevated

24-HOur Vanillylmandelic acid (VMA) test will be elevated

(VMA = epi/norepinephrine metabolite)

30
Q

Tx for pheochromocytoma?

A

Surgical resection (excellent prog)

31
Q

Developmental malignancy of neonates/children <5

Large abd tumor frequently found by parents

Elevated VMA urine test!

A

Neuroblastoma

tx = combo of surgery, rad, chemo

(Early detection = 90% cure)

32
Q

Cushing’s disease AKA….

3 most common causes?

A

… hyper cortisolism tied to ACTH

  1. Pituitary adenoma- produce excess ACTH (70% of cases) = DISEASE
  2. Adrenocortical tumor = excess corticosteroids = SYNDROME
  3. Exogenous glucocorticoids- prolonged steroid tx of AI d/o