Endocrinology Flashcards

1
Q

Normal delay between bone age and chronological age

A

2 years

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2
Q

Genetic/Familial Short Stature

A
  • Born with normal length, but height then decelerates over first 2 years of life to find new genetically determined curve
  • Bone age MATCHES chronological age
  • Proportional in height and weight
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3
Q

Mid-parental height equation

A
  • [Dad’s height + Mom’s height +/- 5 inches or 13 cm]/2

- Add length for boys, subtract for girls

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4
Q

Constitutional growth delay

A
  • Normal growth until about 1 year, then around 3rd - 5th percentile (usually NOT below 3rd percentile)
  • Height matches with bone age films
  • DELAYED BONE AGE + DELAYED PUBERTY (pt still has to hit puberty and will continue to grow)
  • GH NOT indicated UNLESS >2.25 SD below mean (< 1.2%)
  • May consider referral to Endo for short course of testosterone due to psychosocial factors
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5
Q

Short Stature 2/2 Growth Hormone Deficiency

A
  • RARE
  • PE: micropenis, small clitoris, hypoglycemia (look for seizures in hx)
  • DECELERATED growth rate - lines on growth chart crossed
  • Dx: lack of GF release following stimulation with insulin or arginine
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6
Q

Congenital GH deficiency

A
  • Bone age approx. 75% of chronologic age + DECELERATED GROWTH RATE + weight percentile > height percentile (remember w/ constitutional delay, wt/ht will be similar)
  • Typically NOT the answer on boards
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7
Q

Acquired GH deficiency

A
  • Delayed bone age and SHARPLY DECELERATED growth rate

- MUST refer to Endocrinology and obtain MRI to evaluated for CNS tumor

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8
Q

Metabolic Syndrome

A
  • Truncal obesity
  • Low HDL
  • High triglycerides
  • High BP
  • FBG > 100 mg/dL
  • Acanthosis nigricans is NOT part of definition
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9
Q

Diagnosis of Diabetes Mellitus

A
  • Fasting blood glucose > 125 mg/dL
  • 2 hours plasma glucose tolerance test >/= 140 = prediabetes; >/= 200 = DM.
  • Hgb A1C >/= 5.7% prediabetes; >/= 6.5% DM
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10
Q

Differentiating central vs peripheral precocious puberty in males

A
  • Central = testicular volume increased AND/OR LH >/= 0.3 IU/L
  • Also may see increased testicular volume with hCG secreting tumors, though volumes usually smaller than expected for other pubertal signs
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11
Q

Peripheral precocious puberty causes

A
  • May originate from arenal gland, gonad, an hCG-secreting tumor (in boys), exogenous hormone exposure, or severe hypothyroidism.
  • Testicular volume will be prepubertal (with exception of hCG secreting tumor) and LH will be in prepubertal range (< 0.3 IU/L).
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12
Q

Hashimoto thyroiditis

A
  • Most common cause of hypothyroidism and goiter in children
  • AI destruction of thyroid gland
  • Thyroid function may be normal, though at risk of hypothyroidism in the future
  • Thyroid enlarged, firm, rubbery and heterogenous
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13
Q

Thyroid exam in Hasimoto’s vs Grave’s

A
  • Hashimoto’s = enlarged, firm, rubbery, heterogenous

- Grave’s = larger, less firm and more homogenous

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14
Q

Thyroxine-binding globulin deficiency

A
  • X-linked disease
  • NBS reveals normal TSH but LOW T4. NBS measures T4 (bound hormone) -> due to def of binding globulin, T4 is low.
  • Check FREE T4 (normal) or TBG
  • If TSH is normal –> NO treatment is needed
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15
Q

Signs of congenital hypothyroidism

A
  • May be asymptomatic at birth due to maternal thyroxine crossing placenta
  • Puffiness, large tongue, hoarse cry, umbilical hernia, hypotonia, large anterior fontanelle, open posterior fontanelle, constipation, mottling
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16
Q

Most common causes of hypothyroidism

A
  • Dysgensis is MOST COMMON
  • Abnormal thyroid development between base of tongue and normal position - mass is midline, though not cystic
  • Acquired hypothyroidism
  • Hashimoto thyroiditis
17
Q

Management of abnormal TSH on NBS

A
  • Start levothyroxine and order TSH and fT4
  • Cognitive delays may occur if thyroid hormone is not supplied by 2 weeks of age
  • May DC meds later if labs normal
18
Q

Labs with Hashimoto thyroiditis

A
    • anti-TPO
    • anti-thyroglobulin
  • low fT4
  • elevated TSH
19
Q

Most specific marker of adrenal androgen production

A
  • DHEA-S is more specific than testosterone
20
Q

Neonatal Graves Disease

A
  • Maternal thyroid-stimulating antibodies cross placenta. Even if Mom tx with RI ablation, antibodies remain. Mom may be on levothyroxine due to RI ablation.
  • Symptoms present in IMMEDIATE newborn period
  • S/S: tremors, tachycardia, SVT, increased Moro, very alert/awake). May lead to heart failure!!
  • Diagnose with thyroid function panel
  • Tx: methimazole and a β-blocker for a few months until the maternal thyroid-stimulating antibodies wane
  • Of note, maternal levothyroxine has minimal effect on fetus
21
Q

Best laboratory indicator of vitamin D status

A
  • 25-hydroxy vitamin D
22
Q

Effect of prolonged immobilization on calcium

A
  • Causes increased calcium
  • Increased calcium may lead to inhibition of vasopressin (ADH) –> polyuria, polydipsia, HA, nausea and abdominal pain
  • Dx with iCa
  • Tx with saline diuresis and loop diuretics
23
Q

Definition of hypercalcemia

A
  • Calcium > 12
24
Q

Effects of hypercalcemia

A
  • Shortening of ST segment –> shortened QT interval
  • S/S: Bones, stones, groans and moans: Bones (osteoporosis, osteomalacia, pathologic fx, osteitis fibrosis cystica), Stones (nephrolithiasis, nephrocalcinosis, nephrogenic DI), Groans (N/V, constipation, abdominal pain, Moans (coma, delirium, depression, fatigue, psychosis), polyuria, polydipsia, HA
  • Tx with IV hydration. If due to immobilization, tx with loop diuretics (due to inhibition of calcium reabsorption in thick ascending limb).
25
Q

Causes of hypercalcemia

A
  • Familial hypocalciuric hypercalcemia - benign.
  • Williams Syndrome
  • Vitamin D ingestion
  • Vitamin A ingestion
  • Thiazide diuretics (calcium sparing)
  • Skeletal disorders (i.e. dysplasias, skeletal immobilization, skeletal/body casting)
  • Hyperparathyroidism
  • Malignancy