Endocrine Pathophysiology - The Adrenal Gland and Acromegaly Flashcards

1
Q

What is Cushing’s syndrome?

A

A collection of signs and symptoms that occur when a patient has long term exposure to cortisol

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2
Q

Causes of Cushing’s syndrome

A

Exogenous

  • Iatrogenic eg prescription of glucocorticoids for asthma

Endogenous

  • ACTH dependent
    • Cushing’s disease (ACTH is prosuced from a pituitary adenoma)
    • Ectopic ACTH production (usually from small cell lung cancer)
  • ACTH independent: CARS
    • Cancer: adrenal carcinoma
    • Adrenal nodular hyperplasia
    • Rare causes: McCune-Albright syndrome
    • Steroid use
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3
Q

Signs and symptoms of Cushing’s syndrome

A

Round in the middle with thin limbs:

  • Round “moon” face
  • Central Obesity
  • Abdominal striae
  • Cervical fat pad
  • Proximal limb muscle wasting

High levels of stress hormone:

  • Hypertension
  • Cardiac hypertrophy
  • Hyperglycaemia (Type 2 Diabetes)
  • Depression
  • Insomnia
  • Acne
  • Amenorrhoea

Extra effects:

  • Osteoporosis
  • Easy bruising and poor skin healing
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4
Q

Cushing’s syndrome investigations

A
  • Diagnostic tests: urinary free cortisol, low does and high dose dexamethasone suppression test
  • Bloods: FBC, U&Es, LFTs, glucose, lipid levels
  • Radiology: XR (look for lung cancer and vertebral collapse)
  • DEXA (dual energy X-ray) scan
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5
Q

Cushing’s syndrome treatment

A
  • Conservative
    • Advise patients to decrease alcohol consumption since alcohol increases cortisol levels
  • Medical
    • Ketoconazole, metyrapone, fluconazole to decrease cortisol
    • Treat compications
  • Surgical (main treatment)
    • Trans-sphenoidal removal of pituitary adenoma
    • Surgical removal of adrenal tumour
    • Surgical removal of tumour producing ectopic ACTH

If surgical removal of the cause is not possible another option is to remove both adrenal glands and give the patient replacement steroid hormones for life.

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6
Q

Cushing’s syndrome complications

A
  • Osteoporosis
  • Diabetes mellitus
  • Hypertension
  • Immunosupression
  • Cataracts
  • Striae formation
  • Ulcers
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7
Q

What is adrenal insufficiency?

A

Occurs when the adrenal glands fail to produce sufficient steroid hormone

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8
Q

Causes of primary adrenal insufficiency

A
  • Primary
    • Addison’s disease
    • Idiopathic
    • Postadrenalectomy
  • Secondary
    • Prolonged prednisolone use
    • Pituitary adenoma
    • Sheehan’s syndrome
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9
Q

Causes of Addison’s disease

A

MAIL

  • Metastases from breast, lung and renal cancers
  • Autoimmune
  • Infections
  • Lymphomas
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10
Q

Signs and symptoms of adrenal insufficiency

A
  • Unintentional weight loss
  • Myalgia
  • Weakness
  • Fatigue
  • Postural hypertension
  • Skin pigmentation
  • Body hair loss
  • Abdominal pain
  • Diarrhoea
  • Nausea and vomiting
  • Deprssion
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11
Q

Adrenal insufficiency investigations

A
  • Diagnostic tests
    • Adrenocorticotropic hormone (ACTH) and cortisol measurements
    • Insulin tolerance test
    • Short Synacthen test
  • Bloods: FBC, U&Es (↓Na+, ↑K+), LFTs, gucose, lipid levels, serum calcium
  • Radiology
    • CXR (look for lung cancer)
    • CT and MRI scan of the adrenal glands
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12
Q

Adrenal insufficiency treatment

A
  • Conservative
    • Patient must carry a steroid alert card
  • Medical
    • Replace glucocorticoids and mineralocorticoids with hydrocortisone and fludocortisone
    • Treat complications
  • Surgery
    • Surgical excision of tumour if indicated
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13
Q

Complications of adrenal insufficiency

A
  • Adrenal crisis
  • Hyperkalaemia
  • Hypoglycaemia
  • Eosinophilia
  • Alopecia
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14
Q

Addison’s disease is associated with which conditions?

A

3PGH

  • Pernicious anaemia
  • Primary ovarian failure
  • Polyglandular syndrome
  • Grave’s disease
  • Hashimoto’s thyroiditis
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15
Q

What is acromegaly?

A

Acromegaly is a syndrome that results from excessive growth hormone production after fusion of the epiphyseal plates. Excess GH prosuced before epiphyseal plate fusion causes gigantisism.

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16
Q

Causes of acromegaly

A
  • Pituitary adenoma (most common)
  • GHRH production from bronchial carcinoid
17
Q

Signs and symptoms of acromegaly

A
  • Increased jaw size
  • Increased hand size
  • Macroglossia
  • Lower pitch of voice
  • Carpal tunnel syndrome
18
Q

Acromegaly investigations

A
  • Bloods:
    • FBC, U&Es, LFTs, creatinine, glucose, IGF-1 (raised), lipid levels, prolactin levels
    • GH levels, Glucose tolerance test
  • Radiology
    • CXR
    • CT and MRI scan
  • ECG and ECHO: assess for cardiac complications eg cardiomyopathy
  • Visual field testing: bilateral hemianopia
  • Look at old photos if possible
19
Q

Acromegaly treatment

A
  • Conservative
    • Inform patient that bony changes will not revert after treatment
  • Medical
    • Somatostatin analougues eg octerotide
    • Dopamine agonists eg cabergoline
    • GH receptor antagonists eg pegvisomant
  • Surgery
    • Trans-spenoidal surgical excision of the adenoma is the treatment of choice
20
Q

Aromegaly complications

A
  • Increased risk of cardiovascualr disease
  • Hypertension
  • Diabetes mellitus
  • Increased risk of colon cancer
  • Erectile dysfunction
  • Postsurgical eg infection, cerebrospinal fluid (CSF) leak