Endocrinology Flashcards
DIAGNOSIS-MEN ASYMPTOMATIC, WOMEN: CANNOT LACTATE
PROLACTIN DEFICIENCY
DIAGNOSIS-WOMEN: NO OVULATION, AMENORHEIC MEN:NO SPERM,DECREASE HAIR&LABIDO
FHS AND LH DEFICIENCY
DIAGNOSIS-DECREASED FSH,LH FROM LOW GnRH ANOSMIA AND RENAL AGENESIS IN 50%
KALLMAN SYNDROME
DIAGNOSIS-SHORT STATURE, ADULTS FEW SYMPTOMS:CENTRAL OBESITY, INCREASED LDL AND CHOL. REDUCED LEAN MASS
GH DEFICIENCY
DIAGNOSIS- ALL ABOVE SX.
PANHYPOPITUITISM
INITIAL TEST- PANHYPOPITUITISM
HYPONATREMIA, MRI OF PITUITARY
INITIAL TEST- CONFIRM LOW HORMONE PANHYPOPITUITISM WITH LOW TSH, T4 IN BLOOD
DECREASE IN TSH IN RESPONSE TO TRH
INITIAL TEST-CONFIRM LOW HORMONE PANHYPOPITUITISM WITH LOW ACTH AND CORTISOL
COSYNOTROPIN(ACTH)=CORTISOL RISE (ACUTE), CORTICOTROPIN(CRH)=INC.ACTH BUT NO CORTISOL
INITIAL TEST- CONFIRM LOW HORMONE PANHYPOPITUITISM WITH LOW LH, FSH,TEST
NO CONFIRMATORY TEST
TIP- OLDER TESTS FOR PANHYPOPITUITISM
METYRAPONE(CAUSE ACTH LEVEL RISE), INSULIN STIMULATION(CAUSE GH TO RISE)= ABNORMAL SHOULD RESULT OPP.
INITIAL TREAT- PANHYPOPITUITISM
TIP- OXYTOCIN HAS NO DISEASE? TRUE OR FALSE
REPLACE HORMONES: CORTISONE, THYROXINE, TESTOSTERONE/ESTRO,GH
TRUE
P.ASS.-POST- STROKE,TUMOR, TRAUMA HYPOXIA OR INFITRATION OF THE PIT GLAND INFECTION/IFLAM.
P.ASS.-CHRONIC PYELONEPHRITIS, AMYLOIDOSIS, MYELOMA OR SICKLE CELL, HYPERCALCEMIA, HYPOKALEMIA, LI
DIAGNOSIS- POLYURIA AND HYPERNATREMIA (CONFUSION,LETHARGY, SEIZURES /COMA
INITIAL TEST-
INITIAL TREAT-
INITIAL TREAT-
DIABETES INSIPIDUS CENTRAL
DIABETES INSIPIDUS NEPHROGENIC
DIABETES INSIPIDUS
SERUM SODIUM THEN VASOPRESSIN TEST: BETTER IN CENTRAL AND NO CHANGE IN NEPHROGENIC
CENTRAL DI= LONG-TERM VASOPRESSIN (DESMOPRESSIN/ ADH)
NEPHROGENIC DI= TREAT CAUSE:(E.G.HYPOKALEMIA OR HYPERCALCEMIA), HYDROCHLOROTHIAZIDE, AMILORIDE, PROSTAGLANDIN INH (INDOMETHACIN)
P.ASS- PITUTARY ADENOMA, GASTRINOMA OR INSULINOMA OR ECTOPIC GH OR GHRH (LYMPHOMA OR BRONCHIAL CARCINOID)
DIAGNOSIS- INCREASED HAT,RING,SHOE SIZE, CARPAL TUNNEL, ODOR,DEEPVOICE,COLONIC POLYPS,ARTHRALGIAS,HYPERTENSION, CHF, ED
INITIAL TEST- ACROMEGALY
ACC. TEST- ACROMEGALY
INITIAL TREAT- ACROMEGALY
ACROMEGALY
ACROMEGALY
SERUM IGF-1, GLUCOSE (INTOLERANCE), HYPERLIPIDEMIA THEN MRI
GLUCOSE SUPPRESSION TEST
SURGERY (TRANSPHENOIDAL RESEC)OR RADIATION, PHARM:CABERGOLINE(DOPAMINE), OCTREOTIDE OR LANREOTIDE (SOMATOSTATIN), PEGVISOMANT
P.ASS.-INC.GH/TRH(HYPOTHYROIDISM), PIT ADENOMA, PREGNANCY,EXCERISE,RENAL INS.,CHEST STIMULATION, LOW DOPAMINE (DRUGS)
DIAGNOSIS- WOMEM: GALACTORRHEA, AMENORRHEA, INFERTILITY/MEN:ED GYNECOMASTIA
INITIAL TEST- HYPERPROLACINEMIA
INITIAL TREAT- HYPERPROLACTINEMIA
HYPERPROLACTINEMIA
ANTIPSYCHOTICS, METHYLDOPA, METOCLOPROMIDE, OPIOIDS, TRICYCLICS, VERAPAMIL
SERUM PROLACTIN, TFT, PREGNANCY TEST, BUN/CR, LFT THEN MRI(PROBABLE TUMOR)
DOPAMINE AGONIST(CABERGOLINE/BROMOCRIPTINE), TRANSPHENOIDAL SURGERY, RADIATION (RARE)
TIP- DRUGS THAT INCREASE PROLACTIN
DIAGNOSIS- BODILY ROCESSES BEING SLOWED DOWN
INITIAL TEST-
INITIAL TREAT-
HYPOTHYROIDISM
LAB: TSH, T4/T3
IF DOUBLE TSH; THEN= THYROXINE
TIP- COMMON CAUSE OF HYPOTHYROID=HASHIMOTO, DIET, AMIODARONE
TIP- IF TSH IS HIGH BUT NOT DOUBLE RUN? IF POSITIVE THEN WHAT?=ANTITHYROID PEROXIDASE/ANTITHYROGLOBULIN ANTIBODIES THEN TREAT WITH THYROXINE