Pituitary Gland Dysfunction Flashcards

1
Q

What pattern of regulation exists for growth hormone?

A

Pulsatile, Diurnal pattern

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2
Q

Biochemical evaluation requires assessment of _____ and their _____

A

Pituitary hormones and their target gland hormones

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3
Q

Where is the problem for a primary gland failure?

A

High trophic hormone level and low target gland level (Target endocrine gland deficiency)

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4
Q

TSH-oma - what kind of failure is this?

A

Uncommon, easily missed
High target gland hormone and high trophic hormone
Can be:
- autonomous secretion of trophic hormone
- resistance to target gland hormone action

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5
Q

What kind of problem is there for secondary/tertiary gland failure?

A

Low trophic hormone and low target gland hormone

Trophic Hormone Deficiency

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6
Q

What kind of defect may exist with low trophic hormone level and high target gland hormone level?

A

Autonomous secretion of target endocrine gland hormone

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7
Q

Dynamic pituitary testing

A
  1. Hormone excess assessed by: suppression test (ie oral glucose tolerance)
  2. Hormone deficiency assessed by: stimulation test (ie insulin tolerance test)
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8
Q

Problems of GH excess

A
  1. Gigantism - GH excess before puberty

2. Acromegaly - GH excess after puberty (acral bony overgrowth and soft tissue swelling)

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9
Q

What is the best screening test for GH excess?

A

Look for an elevated IGF-1 level (make sure that this is age and gender matched).
Integrated 24 hr secretion. Long half-life.

Tx:

  • Surgery
  • Somatostatin analogs
  • GH receptor antagonist
  • Radiation therapies
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10
Q

Somatopause

A

Changes with aging that may make us flabby. Decline of 14% per decade of GH/IGF-1 levels.

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11
Q

Manifestations of adult GHD

A
Body composition
- inc fat deposition
- dec muscle mass, strength, & exercis
Bone strength
- inc bone loss and fracture risk
Metabolic and cardiovascular effects
- inc cholesterol levels
- inc inflammatory and prothrombotic markers (CRP)
Psychological well-being
- loss of spunk
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12
Q

What is GH not approved for by the FDA?

A
  • Anti-aging
  • Obesity
  • Chronic fatigue syndrome
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13
Q

How do you diagnose AoGHD?

A

Provocative test for GH Reserve = Inducing hypoglycemia

  • this is dangerous
  • do not do in elderly, h/o seizure disorder, CAD, or cerebrovascular disease

Second best test:
GHRH-Arginine test (not available in US), instead we just have Arginine and glucagon stimulation test

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14
Q

Hyperprolactinemia causes

A

PRL level

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15
Q

Prolactinoma presentation

A
  • Most common functional pituitary tumor
  • F:M is 10:1, median age of diagnosis = 34 y/o

Different presentations in men and women

Women:
- microadenoma 1 cm
- no galactorrhoea
- visual field abnormalities
- impotence
- E.O.M. paralysis
(anterior pituitary malfunction)
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16
Q

Diagnosis of prolactinoma

A

Random PRL level (correlate with tumor size)
> 100-150 ng/dl = microadenomas
> 200-250 ng/dl = macroadenomas

Pituitary MRI

17
Q

Prolactin deficiency

A

Etiology: severe pituitary destruction
Presentation: failed lactation in women, no known effect in males
Dx: low basal PRL level

18
Q

Primary functions of cortisol

A
  • Gluconeogenesis
  • Breakdown of fat and protein for glucose production
  • control inflammatory reactions
19
Q

Complications of chronic cortisol excess

A

Cushings Syndrome

  • Changes in carb, protein and fat metabolism
  • Changes in sex hormones
  • Salt and water retention
  • Impaired immunity
  • Neurocognitive changes
20
Q

Endogenous hypercortisolism types and etiologies

A

ACTH - dependent (70-75%)

  • Corticotrope adenoma (Cushing’s)
  • Ectopic Cushing’s (ACTH/CRH tumors)

ACTH - independent (25-30%)

  • adrenal adenomas
  • adrenal carcinoma
  • nodular hyperplasia (micro or macro)
21
Q

What are the high discriminatory features of Cushing’s syndrome?

A
  • Plethoric/moon facies
  • Wide (>1cm) violaceous striae (abdominal and axillary)
  • Spontaneous ecchymoses
  • Proximal muscle weakness
  • Early/atypical osteoporosis (atraumatic rib fx)
22
Q

What are the cortisol rhythms?

A
  • Episodic ACTH/cortisol secretions daily
  • Major ACTH/cortisol burst in early morning
  • Cortisol Nadir 11-12 pm

Note: most cortisol is bound to transcortin, only 5% is free

23
Q

Screening tests for Cushing’s

A
  • Disrupted circadian rhythm (midnight salivary or serum cortisol)
  • Increased filtered cortisol load (24 hr urine free cortisol)
  • Attenuated negative feedback (low dose dexamethasone suppression test)
24
Q

What is pseudo-cushing’s disease?

A
  • Overactivation of the HPA axis, without tumorous cortisol hyper-secretion (ramps up the whole system)
25
How do you work-up Cushings?
1. ACTH level - plasma ACTH levels are high-normal to mildly elevated 2. Imaging - Pituitary MRI, only 50% identified on MRI (surgery if can see, else move on to #3) 3. Inferior petrosal sinus sampling - for a negative/equivocal MRI
26
What are the etiologies of central adrenal insufficiency?
- Most common cause: supraphysiologic exogenous glucocorticoid use - Drugs: opioids and megace - Hypothalamus/Pituitary diseases and their treatments - Other isolated ACTH deficiency (rare)
27
Clinical presentation of AI
- Fatigue - Anorexia, nausea/vomiting and weight loss - Generalized malaise/aches - Scant axillary/pubic hair - Hyponatremia and hypoglycemia
28
Testing for AI
Basal testing: random a.m. cortisol level 18 excludes AI Stimulation testing: - insulin induced hypoglycemia - assess the entire HPA axis - Cosyntropin stimulation test valid for assessing HPA axis only if prolonged loss of pituitary signaling and resulting adrenal atrophy (not good for if someone just comes into hospital acutely)
29
Hypogonadism Differential Dx
High FSH/LH: - Congenital anorchia - Klinefelter's Syndrome - Testicular injury - Autoimmune testicular dz - Glycoprotein tumor (rarely) Low FSH/LH - Macroadenomas, prolactinomas, XRT - Isolated GnRH Deficiency (Kallman's anosmia vs. idiopathinc) - Hemochromatosis - Functional deficiency - Critical illness, OSA, starvation, meds-opiates, glucocorticoids
30
Gonadotropin excess presentation
- Clinically silent - Rare presentation: ovarian hyper-stimulation syndrome or macro-orchidism - Usually middle-aged patient with macroadenomas and related mass effects
31
Gonadotropinoma diagnosis
- Blood tests: low FSH/LH, T/E2 - Pituitary MRI - Immunohistochemical analyses (+ FSH, LH or ASU staining) of resected tumor
32
Etiologies of TSH elevation
Secondary - Thyrotropin secreting pituitary tumor - very rare - Thyroid hormone resistance
33
Clinical presentation of hyperthyroidism
Thyrotropinoma - heat intolerane, hair loss, goiter, tremor, weight loss, diarrhea, irregular menses or mass effects Dx: - Elevated free T4 and a non-suppressed TSH