Endo Flashcards

(131 cards)

1
Q

Percentage of T3 derived from conversion of T4

A

80%

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2
Q

Major thyroid hormone-binding protein

A

Thyronine-binding globulin (TBG)

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3
Q

% of T4 and T3 are bound

A

Greater than 99.5%

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4
Q

Major cause of decreased T3 concentration in patients with a critical illness

A

Impaired peripheral conversion of T4 to T3 secondary to inhibition of deiodination process

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5
Q

Embryonic origin of thyroid gland

A

Median downgrowth of 1st and 2nd pharyngeal pouches in the area of foramen cecum

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6
Q

Embryonic origin of parafollicular cells

A

Ultimobranchial bodies of 4th and 5th branchial pouches
Neuroendocrine cell lineage

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7
Q

Genetic mutation in medullary thyroid cancer

A

RET proto-oncogene

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8
Q

Electrolyte ratio pathognomonic for hyperparathyroidism

A

Serum chloride to phosphate ration >30

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9
Q

Hemodynamics of thyroid storm

A

Tachycardia
Increased CO
Decreased systemic vascular resistance (SVR)

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10
Q

What artery do all parathyroids typically receive their blood supply from?

A

Inferior thyroid

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11
Q

Oncogene of hyperparathyroid

A

Prad oncogene

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12
Q

Bone finding pathognomonic for hyperparathyroidism

A

Osteitis fibrosa cystica

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13
Q

Lab findings in hyperthyroidism

A

Hypercalcemia
Hypokalemia
Hyperglycemia
Hypocholesterolemia
Microcytic anemia
Lymphocytosis
Granulocytopenia
Hyperbilirubinemia
Increase alkaline phosphatase

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14
Q

Initial tx for thyroid storm

A

IV fluids
Hypothermia
Acetaminophen
Propranolol
PTU
Iodine

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15
Q

Single test would allow for differentiation of thyrotoxicosis from acute destruction viral thyroiditis

A

Radioactive iodine uptake (RAIU) test

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16
Q

What inhibits the release of TSH

A

Elevated circulating levels of T3, T4 and somatostatin

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17
Q

45yo
2yr hx of Diffuse, tender thyroid enlargement
Lethargy
20pound weight gain
Dx?

A

Hashimoto’s thyroiditis

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18
Q

Vebous drainage of thyroid gland

A

Superior and middle thyroid vein – Internal Jugular Vein
Inferior thyroid vein – Innominate vein

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19
Q

MC location of recurrent laryngeal nerve

A

Tracheoesophageal groove

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20
Q

Result of bilateral injury to Superior laryngeal nerve

A

Swallowing disorders

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21
Q

Single most important test in the diagnostic work up of patients with solitary thyroid nodule

A

FNA

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22
Q

Which thyroid malignancy does radiation increases the incidence

A

Papillary cell CA

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23
Q

This is a variant of follicular cell ca
SIZE is the only predictor of malignancy
Associated with history of Hashimoto’s thyroiditis

A

Hurthle cell CA

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24
Q

5cm thyroid nodule
FNA - fluid, nodule disappeared, cytology benign
Next step?

A

Total thyroid lobectomy with isthmusectomy
- increased chance of malignancy in large cysts (>3cm)

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25
No risk factor (+) thyroid jodule FNA is non diagnostic (follicular cells) Tx of choice?
Thyroid lobectomy with isthmusectomy If follicular CA, secondary sx for completion total thyroidectomy w postop I-131 is indicated
26
Factor best correlates w presence of LN metastasis in papillary CA
Age
27
Tx of choice for patients with papilary thyroid ca without clinical evidence of LN metastasis
Total thyroidectomy
28
Pt with very highCalcium Palpable roch hard neck mass Dx?
Parathyroid carcinoma Tx Wide excision with en block resection of adjacent thyroid tissue
29
Neuroendocrine cell etiology Can occur throughout GI tract or bronchi Flushing, diarrhea, R sided heart failure most commonly occurs with metastatic disease and mid-gut tumors
Carcinod tumor Tx: Octreotide Isolated mets can be resected
30
Follicular carcinoma metastases occur primarily by?
Hematogenoys dissemination to lungs, bones and other peripheral tissues
31
Confirmation of follicular thyroid CA
Indentification of Vascular or Capsular invasion by tumor from histologic section
32
Surgical tx of medullay thyroid CA
Total thyroidectomy w Central node dissection, lateral cervical LN samplinv of palpable nodes and a modified radical neck dissection, if positive
33
Germline defect in what gene responsible for Multiple Endocrine Neoplasia (MEN2a and 2b) and Familiar Medullary Thyroid CA (FMTC)
RET Proto-oncogene - should undergo prophylactic thyroidectomy before 10yo
34
Histo caharacteristic of Medullary thyroid CA (MTC)
Congo red dye (+) Apple green birefringence consistent with amyloid Immunihistochemistry (+) for cytokeratins, CEA and Calcitonin PARAFOLLICULAR C CELLS are the precursor to tumor cells
35
(+) Medullary thyroid CA High urinary Vanillylmandelic acid (VMA) Enlrged left adrenal gland Management?
Alpha and beta blockers Then resection of left adrenal gland --should be performed before thyroid sx
36
Embryological origin of parathyroid gland
Inferior parathyroid - 3rd pharygeal pouch Superior parathyroid - 4th pharyngeal pouch
37
Etiologies of hypercalcemia
Hyperparathyroidism Paraneoplastic syndrome Metastatic CA Bone metastasis Milk-alkali syndrome Sarcoidosis
38
Effect of PTH on intestinal absorption of calcium
PTH stimulates vit D hydroxylation in the kidney and increases intestinal absorption of calcium
39
Calcitonin is produced in?
Parafollicular cells (C cells) of thyroid
40
Serum Calcium of 13 mg/dL Serum PTH 400 mEq/mL Dx?
Prinary hyperparathyroidism
41
Serum Calcium of 8.5 mg/dL Serum PTH 400 mEq/mL Serum creatinine 5.6mg/dL Dx?
Secondary hyperparathyroidism
42
Appropriate management if thr 4th Parathyroid hormone cannot be located by intraoperative utz
Terminate the operation for localization studies
43
Problem if injured external branch of superior laryngeal nerve
Loss of High-pitched tone
44
Components of MEN 1 syndrome
Parathyroid hyperplasia (90%) Islet cell Neoplasms (30-80%) Pituitary tumors (15-50%)
45
Tx of choice pt w hyperparathyroidism associated MEN 1 or MEN 2 Also secondary hyperparathyroidism
Subtotal (3 ½ gland) parathyroidectomy or total parathyroiderctomy w autotransplantation in the FOREARM
46
1st line therapy for patients with marked hypercalcemia and/or severe symptoms
IV hydration followed by furosemide
47
Idication of calcium supplement after thyroid or parathyroid sx
Circumoral paresthesia, anxiety, positive Chvostek's or Trousseau's sign, tetany, ECG changes or serum calcium less than 7.1 mL/dL
48
In a nonacute setting, what is the max useful amount of calcium supplementation
2g calcium/d
49
Appropriate Calcium suppplementation if max amount of calciun has already been given and patient still hypocalcemic
Calcitriol or other vit D preparations
50
Medullary thyroid carcinoma Pheochromocytoma Mucosal neuromas Ganglioneuromas MARFANOID habitus Dx?
MEN 2b
51
Zone of adrenal gland spared in autoimmune adrenal disease
Medulla
52
Secretion of which adrenal hormone NOT impaired by secondary adrenal insufficiency
Aldosterone
53
MC cause of chronic primary adrenal insufficiency (Addison's disease)
Autoimmune disease
54
MC cause of acute secondary adrenal insufficiency
Steroid medication withdrawal Sheehan's sybdrome (postpartum Pituitary necrosis) Bleeding into a pituitary macroadenoma Head trauma
55
Posterior pituitary secrete?
ADH and Oxytocin
56
Anterior pituitary secrete?
Growth hormone (GH) Adrenal corticotropin hormone (ACTH) TSH LH FSH Prolactin
57
Therapy should be istituted to obtaininv the results of ACTH stimulation test in a critically ill patient
Empiric stress dose of DEXAMETHASONE
58
Basis of insulin-induced hypoglycemia test for patients with secondary adrenal insufficiency
Hypoglycemia induced by 0.1 unit of insulin/kg stimulates the entire hypothalamus-hypophyseal-adrenal axis (HPA) and the sympathetic nervous system Plasma cortisol level should exceed 20g/dL
59
Decreased SVR Hypotension with high CO Normal filling pressure Hypoglycemia Dx?
Hemodynamic pattern of patient with ADRENAL INSUFFICIENCY
60
Daignostic test best predictor of adrenal adequacy in patients previously receiving steeoids, who are scheduled for surgery
Peak corrisol level after administration of corticotropin
61
45yo male Hypotension and lethargy Henoglobin 12g/dL Blood glucose 34mg/dL 24 hrs after colectomy Hx renal transplant 3 years ago Dx?
Addisonian crisis
62
What inhibits GH secretion
Somatostatin
63
Where aldosterone exert its primary effect
Distal tubules and collecting Ducts of the kidney
64
Effect of aldosterone in kidney
Increases absorption of Sodium from urine in exchange for Potassium, aiding in water retention and restoring intravascular volume
65
Catecholamines in stress
Increase Glycogenolysis Gluconeogenesis Lipolysis Ketogenesis Inhibit insulin use in peripheral tissue
66
Function of angiotensin II
VasoCONSTRICT Cardiac stimulation Stimulation of ADH, aldoaterone and thirst
67
Stimuli causes release of ADH (vasopressin)
Plasma osmolality greater than 285 mOsm/L Decrease circulating blood volume, catecholamines, renin-angiotensin system and opiates
68
Inhibits release of LH in male adult
Androgens synthesized by testes
69
Function if FSH in adult female
Stimulates maturation of the Graafian follicle and production of estradiol
70
Limits secretion of ACTH and corticotropin-releasing factor (CRF)
Circulating levels of ACTH
71
GH released in bursts when?
3-4 hrs after meals and during stage III and IV sleep
72
Inhibits release of Prolactin
Dopamine
73
Main physiological stimulus of prolactin release
Suckling of breast
74
Drug interferes with release of dopamine into pituitary portal circulation and enhances prolactin secretion
Metaclopramide Haloperidol Chlorpromazine Reserpine
75
Patient with ACTH deficiency What test will distinguish a hypothalamic CRH deficiency from pituitary ACTH deficiency
CRH stimulation test
76
Dx if absent ACTH responsiveness to CRH
Pituitary corticotropin deficiency
77
Two test will stimulate the entire HPA
Insulin-induced hypoglycemia test Glucagon test
78
Condition defined by a relative or absolute insuffeciency of vasopressin secretion from posterior pituitary
Diabetes insipidus
79
How to diagnose central DI
Water deprivation test
80
Tx of choice for central DI
Exogenous vasopressin
81
Postpartum failure to lactate Postpartum amenorrhea Progressive signs and symptoms of adrenal insufficiency Dx
Sheehan's syndrome
82
MC type of pitutary adenoma
Prolactin-secreting and null-cell (chromophobe adenoma)
83
MC functional pituitary tumor
Prolactinoma
84
MC presenting symptom of prolactinoma in females
Secondary amenorrhe
85
Pharma agent effective in reducing serum prolactin, tumor mass and inhibit tumor growth
Bromocriptine (dopaminergic agonist)
86
Hypersecretion of ACTH by pituitary
Cushing disease
87
Hypertension DM Goiter Hyperhidrosis
Metabolic manifestation of acromegaly
88
Confirmatory test for acromegaly
Glucose suppresion test Oral 100g of glucose fail to supress the GH level to less than 5ng/mL at 60mins
89
Tx of GH producing pituitary adenoma
Surgical excision Medical - octreotide
90
Surgucal approach to pituitary
Transnasal Trans sphenoidal approach
91
Hormones synthesized and secreted by adrenal CORTEX
Cortisol Aldosterone Adrenal androgen Estrogen
92
Hormones synthesized by adrenal MEDULLA
Epinephrine Norepinephrine Enkephalins Neuropeptide Y Corticotropin-releasing hormone
93
Adrenal Corticosteroid hypersecretion
Cushing SYNDROME
94
Pt with palpitations Headache Emesis Pounding pulse Retinitis Dx?
Pheochromocytoma
95
Embryonic origin of adrenal cortex
Coelomic mesothelial cells
96
Embryonic origin of adrenal Medulla
Ectodermal neural crest cells
97
Primary neurotransmitter of sympathetic postganglionic fibers
Norepinephrine
98
Ectopic adrenal medullary cells located lateral to aprta, near origin of inferior mesenteric artery
Glands of Zuckerland
99
Arterial supply of adrenal gland
Superior suprarenal artery Inferior suprarenal artery Branch from Inferior phrenic artery
100
Innervation of adrenal medulla
Preganglionic sympathetic neuron from celiac and renal plexus via splanchnic nerves
101
Drainage of Right adrenal vein
Posterior Inferior vena cava
102
Most circulating plasma cortisol is bound to this protein
Cortisol-biding globulin (CBG) , although small amounts are bound to albumin and other plasma proteins
103
Effect of glucocorticoids on insulin and glucagon
Stimulates production of glucagon and inhibit secretion of insulin
104
Aldosterone physiologic action
Reabsorb Sodium and excretion of Potassium, Hydrogen, and ammonia from the renal tubules Stimulates active sodium and potassium transport in epithelial tissue (sweat glands, GU mucosa and saliva)
105
MC cause of Cushing Syndrome
Pituitary adenoma
106
MC causes ectopic ACTH secretion
Small Cell CA of lung
107
Expected result of Dexamethasone supression test in a pt with ectopic source of ACTH secretion
Dexamethasone should fail to supress cortisol secretion
108
Sex steroids produced in?
Zona reticulosis of adrenal cortex
109
Initial eval in pt suspected to have Cushing's syndrome
Urinary-free cortisol level (markedly elevated) and a low dose decamethasone supression test (no supresion of cortisol)
110
Elevated cortisol Elevated plasma ACTH Persistent elevation of free cortisol after low and high dose dexamethasone administration
Ectopic source of ACTH
111
Useful test to differentiate hypercortisolism caused by pituitary source of ACTH vs ectopic source of ACTH
Dexamethasone supression test Metyrapone test
112
MC cause of primary hyperaldosteronism
Solitary adrenal adenoma
113
Enzymatic deficiency associated with most cases of adrenogenital syndrome (Congenital Adrenal Hyperplasia)
21- hydroxylase
114
Marked hyperpigmentation of skin and visual disturbance Dx,
Nelson syndrome
115
MC cause of acute adrenocortical insufficiency
Withdrawal of chronic steroid therapy
116
MC cause of Spontaneous adrenal insufficiency
Autoimmune dectruction of adrenal glands (>80%)
117
MC associated disorder in pt with autoimmune adrenocortic insufficiency
Hashimoto's thyroiditis
118
Acute adrenal hemorrhage secondary to sepsis (classically meningococcal)
Waterhouse-Freiderichsen syndrome
119
Most useful test to evaluate pt suspected having adrenocortical insufficiency
Rapid ACTH stimulation test
120
Test of choice to distinguish hyperplasia from an adenoma as the cause of primary hyperaldosteronism
Measure plasma aldosterone concentration after change in posture ** only pt with adenoma experience postural decrease in aldosterone**
121
Serum abnormalities seen in functional cortisone secreting adrenal adenoma
High 24hr urine cortisol Low ACTH level
122
Stimuli causes adrenal secretion of catecholamines
Hypoxemka Hypoglycemia Change in temp Pain Shock CNS injury Local wound factors Endotoxin Severe respiratory acidosis
123
Dx test to confirm Pheochromocytoma
Urine metanephrines
124
MC location of Neuroblastoma
Intra abdominal or retroperitoneal (60-70%)
125
Classic electrolyte finding in hyperaldosteronism
Hypernatremia Hypokalemia
126
Syndromes associated with pheochromocytoma
MEN2a MEN2b Von Recklinghausen disease Tuberous sclerosis Sturge-weber disease
127
Stimulates uterine contraction during labor Elicit milk ejection by myoepithelial cells of the mammary ducts
Oxytocin
128
Onlu hypervascular pancreatic neoplasm in angiography
Pancreatic Neuroendocrine tumors
129
Fasting glucose <45 and relief of symptoms with glycose High N and C trrminus of insulin in blood (exogenous insulin with C terminus only) Most common islet tumor and benign in 90% of cases
Insulinoma
130
High malignant potential Most frequent islet cell tumor in MEN syndromw High gastrin level Severe peptic ulcer disease Most located in gastrinoma triangle between CBD/cystic duct junction, 3rd portion of duodenum and gallbladder
Gastrinomas
131
Order of sympathetic blocking medication administration preoperatively for pheochromocytoma
Alpha blocking preoperative (PHENOXYBENZAMINE) with PRN periop B blockade as 2ndary measure