Conditions & Diseases Flashcards

1
Q

Benign pituitary adenomas summary

A

Def: tumor of on one of the type of cells in the pituitary gland

MC is prolactinoma

SS:
Hormone hypersecretion
headache
bitemporal hemianopia
leads to hyposecretion of other hormones
Eval:
MRI w/ contrast - gold
CT
Visual field testing
Serum Hormone level
- prolactin
- TSH, FT4
- ACTH, AM cortisol
- LH, FSH, estradiol, testosterone
- Insulin-like growth factor-1
Monitoring:
>= 10 mm and no abnormalities
- monitor every 6/12 mths and then for next few years
5-9 mm and no abnormalities
- MRI bid next 2 years
2-4 mm and no abnormalities
- no testing needed

Txt:

  • Pharm - dopamine agonists, somatostatin analog, pegvisomant
  • transsphenoidal Surgery
  • radiotherapy
  • gamma knife radiosurgery
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2
Q

Hypersecretion of Growth Hormone summary

A

Def: Excessive release of GH due to GH-secreting pituitary adenoma

SS:
Kids - Gigantism
Adults acromegaly
- feet
- hands
- facial features

Eval:
Serum IGF-I (most sensitive)
Oral Glucose Tolerance Test (specific)

Txt:
Surgery
Somatostatin analogs
GH receptor antagonist

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3
Q

Growth Hormone Deficiency summary

A

SS:
Kids
• Growth retardation
• Short stature (> 3 SD) • Fasting hypoglycemia

Adulthood:
•  Increased abdominal adiposity
•  Reduced muscle strength and exercise capacity
•  Reduced muscle mass
•  Glucose interolerance and insulin
resistance
•  Lipid profile abnormalities
•  Other sxs of panhypopituitarism

Eval:
Low Serum IGF-I screen
Insulin tolerance test
- if normal will increase GH

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4
Q

Hyperprolactinemia summary

A

Def: overproduction of actin

SS:
Women - MC
- Amenorrhea
- galactorrhea
- infertility
- estrogen deficiency
* osteopenia
* vaginal dryness
* hot flushes.

Men:
• Loss of libido and erectile dysfunction

Cause: Prolactinomas and Medications blocking dopamine

Eval:
Preg test
TSH (hypo)
medication effects
MRI
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5
Q

Hypoprolactinemia summary

A

Def: inability to lactate after delivery

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6
Q

Cushing’s syndrome summary

A

Def: Constellation of clinical features from excess glucocorticoids of any etiology

Cause:

  • Pituitary tumor secreting ACTH
  • Secretion of ACTH by non-pituitary tumor
  • ACTH independent tumor of the adrenal gland
  • Iatrogenic
SS:
• Moon facies 
* Obesity
•  Diabetes mellitus
•  Diastolic hypertension
•  Hirsutism
•  Striae
•  Buffalo hump
•  Central adiposity
•  Hyperpigmentation with ectopic ACTH production

Eval:
• Initial tests
- 24 hour urinary free cortisol excretion increased 3 times
above normal
- Dexamethasone overnight test (Plasma cortisol >50 nmol/L at 8-9 AM after 1 mg dexamethasone at 11 PM
- Midnight plasma cortisol >130mnol/L
• Imaging Studies
- MRI pituitary to look for pituitary adenoma
- CT adrenal glands to look for adrenal tumor

Txt:

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7
Q

Adrenal Insufficiency summary

A

Cause:

  • MC autoimmune
  • autoimmune polyglandular syndrome (APS)
  • infection
  • hemorrhage
  • infiltration
SS:
•  weakness/Fatigue
* pigmentation of skin
•  Weight loss
* Ab pain
•  Anorexia
•  Myalgias and arthralgias
•  Fever
•  Anemia, lymphocytosis, eosinophilia •  Hypoglycemia
•  Hypotension (postural)
•  Hyponatremia

Eval:

  • Short ACTH stimulation test
  • ECG
  • Antiadrenal antibodies
  • Evaluate for infections, e.g. adrenal TB
  • 24 hour urine
  • MRI of pituitary to rule out pituitary adenoma
  • Screen for Autoimmune Polyglandular Syndrome

Txt:
IV hydrocortisone
oral hydrocortisone

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8
Q

Diabetes insipidus summary

A

Def: deficiency of ADH

SS:

  • Polyuria
  • polydipsia
  • nocturia
  • Central: posterior pituitary fails to secrete ADH
  • Nephrogenic: kidney fails to respond to ADH
Eval:
•  Water deprivation test
- Normal:
* decrease in urine output
* increase in urine concentration
- DI:
* Continue high urine output
* Continue low urine osmolarity
* Administration of vasopressin
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9
Q

Syndrome of Inappropriate ADH summary

A

Def: excess ADH

SS:
water retention
concentrated urine

Eval

  • Hyponatremia
  • Serum hypoosmolality
  • High urine osmolality (above 100 mosmol/kg)

Txt:

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10
Q

Graves Disease

A

Def: most common hyperthyroid diagnosis; autoimmune disorder; multisystem syndrome

Etiology: women > men; peak age 20-40 yo
Assoc with other AI diseases (type 1 DM, vitiligo, pernicious anemia, collagen vascular diseases)

Patho: Thyroid antibodies (IgG) override regulation which causes overstimulation of thyroid&raquo_space;>increase in thyroid hormone secretion (*this suppresses TRH and TSH)

S/s: diplopia, lacrimation, photphobia, heat intolerance, tachycardia; pretibial myexedema, exopthalmos, lid lag, EOM paralysis, periorbital edema, papilledema, goiter (3x normal, may hear bruit, NON TENDER), ocular manifestations

  • Sympathetic hyperactivity:most pts affected by lid lag which resolves with tx
  • infiltrative changes: immune-mediated orbital edema, protrusion, retinal damage that does not resolve with tx
Tx: 
antithyroid drug therapy
- Propylthiouracil
- Methimazole
radioactive iodine I131
subtotal thyroidectomy
adjuvent sx tx (many will block conversion of T4 to T3)
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11
Q

Multinodular Goiter

A

Def: enlargement of the gland d/t follicular cell numbers increasing; if these cells are functioning they produce thyroid hormone leading to hyperthyroidism

Etiology: hypothyroid/increased thyroid hormone needs (body is trying to make more so it gets larger and then overproduces); hyperthyroidism; infectious or genetic disorders

Patho: hormone levels vary (euthyroid/hypoerthyroid/hypothyroid)

Tx: antithyroid drug therapy; radioactive iodine I131; subtotal thyroidectomy; adjuvent sx tx (many will block conversion of T4 to T3)

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12
Q

Thyroid Nodules

A

Def: less numerous or solitary (adenoma: nodule made of follicular cells that overgrow the area) can lead to toxic/hyperfunctioning if hyperthyroidism follows nodule

Eval: Refer to endocrinology; US; RAIU with I123 to determine hot (area of activity) vs. cold (area of no activity most likely malignant); biopsy; consistent f/u

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13
Q

Subacute thyroiditis (can be both hypo or hyperthyroidism)

A

Def: inflamm of thyroid gland; follicular cell damage so it releases stored thyroid hormone unnecessarily

S/s:*often following a viral infection; *TENDER gland is a hallmark sign; sore neck with fever
elevated thyroid hormone levels, suppression of TSH and TRH

Tx: antithyroid drug therapy; radioactive iodine I131; subtotal thyroidectomy; adjuvent sx tx (many will block conversion of T4 to T3)

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14
Q

Hashimoto’s thyroiditis

A

Def: most common adult cause of hypothyroidism; autoimmune disorder

Etiology: women > men; mean age of dg xis 60

Patho: IgG affects the thyroid and prevents the release thyroid hormone

S/s: often assoc with firm goiter, myexedema, puffy face, extra weight, thickened skin

Tx:
d/c or lower dose of offending medication
Levothyroxine
annual TSH monitoring

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15
Q

Myxedema coma

A
life threatening complication of hypthyroidism
long standing disease
extreme hypothermia
areflexia
seizures
CO2 retention
bradycardia
widespread edema
respiratory depression
coma
almost always in elderly

Tx: URGENT
d/c or lower dose of offending medication
thyroid hormone preparations-synthetic T4 preferred
annual TSH monitoring

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16
Q

Papillary Carcinoma

A

The most common (80% of all thyroid cancer)
Most prevalent 40-80 years old
Mets to nodes common at dx
Long term survival/cure excellent

17
Q

Type 1 Diabetes Mellitus Summary

A

Def: metabolic disorder with abnormally increased blood glucose concentration

Cause: absolute insulin deficiency due to Beta cell destruction via autoimmune system

SS:
polyuria
weight loss
dehydration
N/V
ab pain
blurred vision
diabetic ketoacidosis

Eval:
FPG >=126 mg/dl
Hbg A1C >=7

Txt:
Insulin

18
Q

Type 2 Diabetes Mellitus Summary

A

Def: metabolic disorder with abnormally increased blood glucose concentration

Cause: Insulin resistance and progressive insulin secretory defect (Beta cell dysfunction)

SS:
asymptomatic
blurred vision
retinopathy
metabolic syndrome
Eval:
Test post prandial glucose and C-peptide
Identify immunologic markers of:
- islet cell antibodies
- insulin auto-antibodies
- glutamic acid decarboxylase antibodies
Txt:
Metformin
Sulfonylureas
Meglitinides
Thiazolidinediones
alpha-glucosidase inhibitors
DPP-4 inhibitors
GLP-1 receptor agonists
Amylin mimetics
Bile acid
Dopamine-2 agonists
Sodium-glucose co-transporter 2 inhibitor
Insulin
19
Q

Gestational Diabetes Mellitus summary

A

Def: onset of glucose intolerance during pregnancy around 24-28 weeks

Cause: Increased insulin resistance due to pancreas not being able to keep up with increasing insulin needs

Eval:
FBG
A1C

Txt: exercise
insulin

20
Q

Diabetic Ketoacidosis summary

A

Def: acute, severe life-threatening complication of mainly DM I

SS:
V/N
anorexia
ab pain
hyperventilation
fever
kussmaul respirations with fruity breath
hyperglycemia
dehydration
ketoacidosis
Risks:
Infection
Inflammation
Insufficient Insulin
Intoxication
Ischemia
Eval:
serum glucose > 250
betahydroxybutyrate
pH < 7.3
bicarbonate < 18
anion gap > 12
txt:
hydration
- normal saline
electrolytes
insulin
acid-base balance
- bicarbonate
- potassium
sequelae:
venous thrombosis
ARDS
UGI bleed
Pancreatitis
21
Q

HHS Summary

A

Def: metabolic emergency where induce hyperosmolar state usually in DM II

Cause:
hyperglycemia

Eval:
Dehydration
severe volume depletion
glucose > 600
weight loss
polyuria
polydipsia
lactic acidosis
Txt:
Normal saline
insulin
potassium
monitor renal function
22
Q

Hypoglycemia summary

A

Def: blood glucose < 70 mg/dl

Cause: usually DM I due to insulin overdose

SS:
asymptomatic
diaphoresis
N
Irritability
Hunger
Pallor
Seizures
Coma
Brain damage
death

Eval:

Txt:
glucose
OR
(eat/drink 15 grams carbs; test 15 min; eat 15 carb more)
glucagon
education
23
Q

Hyperparathyroidism

A

S/s: depression, fatigue, loss of appetite, constipation, osteoporosis, kidney stones
(+) Trousseau’s sign: temporarily occluded arterial blood flow above the normal systolic pressure the hands and fingers will contract from ischemia
(+) Chvostek’s sign: tap on facial nerve just below the temple and nose, eye, lip and facial muscles twitch

Tx: decrease high serum levels and possibly remove parathyroid

24
Q

Hypercalcemia

A

Cause* 90% of all pts either have hyperparathyroidism or malignancy

Complications
*stones (kidney), bones (MS), moans (GI-PUD, pancreatitis), and psychic groans (personality changes, LOC)

Tx: identify and tx underlying cause

25
Q

Hypocalcemia

A

Cause: * MC is vitamin D deficiency

S/s: V/D, nervousness, weakness, HA, paresthesias, muscle stiffness, muscle cramps, pain

26
Q

Cushings Disease summary

A

Def: excess production of glucocorticoid hormones

cause:
- adrenal
- pituitary
- steroid
- malignancy

SS:
mood changes
easy bruising
weakness
weight gain
menstrual changes
back pain
HTN
Hirsutism
glucose intolerance
osteoporosis
Eval:
Dexamethasone Suppression Test
CT
MRI
CT abdomen
27
Q

Hypopituitarism summary

A

Def: clinical syndrome of deficiency in pituitary hormone production

Cause:
Tumors
infiltrative processes
infections
ischemia/infarction
empty sella syndrome
iatrogenic
SS:
gonadotropin deficiency
TSH deficiency
GH deficiency
ACTH deficiency
ADH deficiency

Eval:
MRI
CT
cortrosyn stimulation testing

28
Q

Pheochromocytoma summary

A

Def: paroxysmal HTN

SS:
6 H's
- HTN
- HA
- hyperhidrosis
- Heart consciousness (palpitations)
- hypermetabolism
- hyperglycemia
Eval:
Plasma free metanephrines
urine metanephrines
adrenal MRI or CT
MIGB scan

Txt:
Meds
Surgery

29
Q

Obesity overview

A

Def:
overweight >= 25 - 29.9
BMI >= 30
Morbidly obese >= 40

Cause:
genetics
diet
portion distortion
less physical activity

Eval:
BMI
Waist circumference
waist-hip ratio

Txt:
Lifestyle
Meds
- Orlistat
- Phentermine
- Diethylpropoin
- Phentermine/topiramate
- Lorcaserin
- Naltrexone/Bupropion
- Liraglutide
Surgery