Endocrine Flashcards

1
Q

Parathyroid gland oxyphil cells

A

Appear after puberty

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2
Q

Hypoparathyroidism symptoms

A

Tingling in hands, muscle cramps, depression, paranoid, convulsions, psychosis

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3
Q

Pseudohypoparathyroidism

A

Hypocalcemia and ELEVATED, cAMP response to PTH is impaired

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4
Q

Primary hyper parathyroidism

A

Excessive secretion of PTH

Hypercalcemia, elevated PTH, low phosphorus

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5
Q

Non toxic goiter

A

Ability to produce thyroid hormone is impaired, TSH secretion is increased, usually iodine deficiency

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6
Q

Diffuse vs. multi nodular non toxic goiter

A

Diffuse- diffusely enlarged, adolescents and pregnancy

Multi nodular- chronic, irregular nodules, large amount of colloid, people over 50

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7
Q

Cretinism hypothyroidism

A

Usually thyroid dysgenesis, usually infants

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8
Q

Graves hyperthyroidism

A

IgG antibodies to bind to TSH receptor, anti TSH receptor antibodies stimulate thyroid hormone synthesis

Bulding eyes, highly vascular, dark and red, muscle wasting, etc.

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9
Q

Toxic multi nodular goiter hyperthyroidism

A

Women over 50, accumulation of iodine in one or two nodules

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10
Q

Hashimoto thyroiditis

A

T cells stimulate antibody production, induce cell death from CD8 T cells. Leads to hypothyroidism, circulation antibodies and elevated TSH

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11
Q

Papillary thyroid cancer

A

20-50 ages, mostly females, dense fibrosis, nuclear atypism, pale and firm on exam, typically invades cervical lymph nodes

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12
Q

Thyroglossal duct cyst

A

Failure of duct to involute completely, cystic fluid filled remnant, common in children, surgery to remove

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13
Q

Dowager’s hump

A

Indicated the presence of multiple vertebral fractures and decreased bone volume in the elderly, may be a sign of osteoporosis

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14
Q

Primary osteoporosis lab tests

A

Serum calcium, phosphate, and PTH are normal , alk phos would be elevated in a fracture, vitamin D deficiency is common

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15
Q

Bone densitometry scores

A

> -1 is normal

Between -1 and -2.5 is osteopenia

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16
Q

Rickets/osteomalacia

A

Epiphyses of the bone are open, inadequate mineralization of the newly formed bone matrix

**vitamin D deficiency important in this disease process

Bowed legs, milk-looser zones, low calcium and phosphate with high alk. Phos lab, aches and pains, fractures

17
Q

Acidophilic cells

A

Lactotropes and somatotropes

18
Q

Sheehan syndrome

A

Ischemic necrosis of the gland, often from hypotension due to post partum hemorrhage

Clinical cause of panhypopituitarism

19
Q

Hemochromatosis

A

Iron deposits in the pituitary, destroying the gland

Clinical cause of panhypopituitarism

20
Q

Macroadenoma effects

A

Impingement of optic chiasm, invasion of cavernous sinuses (palsies), invasion of hypothalamus (temp regulation, hyperphagia)

21
Q

Lactotrope adenoma

A

Hyperprolactemia, chromophobic, psammoma bodies and endocrine amyloid deposition

22
Q

Somatotrope adenoma

A

Excess secretion of growth hormone, gigantism or acromegaly

Acidophilic with abundant secretory granules- slow growing
Chromophobic with sparse granules- fast growing and invasive

23
Q

Corticotrope adenoma

A

Excess ACTH, Cushing syndrome, typically microadenoma

Basophilic
If chromophobic, more aggressive

24
Q

Cushing syndrome

A

Moon facies, abdominal striae, central obesity.

Found in corticotrope adenoma

25
Q

Gonadatrope adenoma

A

Mainly middle aged men, headaches/visual disturbances/hypogonadism.

Mainly macroadenoma, chromophobic or somewhat acidophilic

26
Q

Thyrotrope adenoma

A

Rarest, hyperthyroidism, goiter, TSH and thyroid hormone increase.

Chromophobic, PAS positive, polyhedral or columnar cells, secretory granules

27
Q

Central diabetes insipidus

A

Due to diease of posterior pituitary, unable to concentrate urine due to lack of ADH (poluria, thirst, polydipsia)

28
Q

SIADH

A

Water retention, weight gain, hypo osmolality of the blood

29
Q

Parathyroid gland chief cells

A

Make PTH