L05 - Adrenal Causes of Hypertension Flashcards

1
Q

Layers of adrenal gland

A

Gomerulosa, Fasciculata, Reticularis

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2
Q

Adrenal causes of hypertension

A

Primary Hyperaldosteronism
CONN’s syndrome
— zona glomerulosa (adenoma, hyperplasia, rare genetic causes)

Phaeochromocytoma (Phaeo)
— adrenal medulla tumour

[[Some forms of congenital adrenal hyperplasia]]

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3
Q

pathway map for aldosterone secretion

A

liver produces angiotensinogen, kidney produces renin which converts to angiotensin i, then ACE converts to angiotensin ii, then aldosterone.

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4
Q

Primary hyperaldosteronism

who to screen. what do they have more of

A

Hypokalaemia, resistant hypertension, younger people

have more vascular and renal pathology than essential hypertension

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5
Q

Primary hyperaldosteronism

what to screen (tests)

tests for specidic aetiology

A

initial tests
supressed renin, normal/high aldosterone

confirmary tests
oral or IV Na+ suppression test

to see if its for secreting adeoma or bilateral hyperplasia:

  • -Adrenal CT scan
  • -Adrenal venous sampling
  • ———-Is the aldo secretion unilateral?
  • -Metomidate PET CT
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6
Q

Primary hyperaldosteronism

treatments

A

Unilateral Adenoma

  • —-Laparoscopic Adrenalectomy
  • —Medical Treatment ( sometimes )

Bilateral Hyperplasia
—-Medical Treatment ( Aldosterone Antagonists) - eg Spironolactone, Eplerinone

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7
Q

Adrenal medulla

what is it

what connected

what does it secrete

A

Modified Post-Ganglionic Nerve cells inervated by preganglionic nerves

symp neurones in spinal cord

tyrosine –> LDOPA–> dopamine–> NA—(cortisol)–> adrenaline

last 3 are catecholamines

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8
Q

Catecholamines

what are they what are the biological effects

A

Noradrenalin (Alpha 1 & 2 )

  • -Vasoconstriction
  • —-Increased BP
  • —-Pallor
  • -Glycogenolysis

Adrenalin ( Alpha 1, Beta 1 & 2 )

  • -Vasoconstriction
  • -Vasodilatation in Muscle
  • -Increased heart rate
  • -Sweating
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9
Q

Phaechromocytoma

Presentation

A

“Spells”

    • Headache, Sweating
    • Pallor, Palpitation
    • Anxiety

Hypertension

    • Permanent
    • Intermittent

Family history

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10
Q

Phaeochromocytoma

genetic conditions associated, symptoms of them

A

Neurofibromatosis Type 1
( NF1 )
—neurofibromas, axillary freckling

Multiple Endocrine Neoplasia type 2
( MEN 2 )
— medullary carcinoma of thyroid gland

Von Hippel – Lindau Syndrome

  • – retinal hemangioglioblastoma
  • – cerebellar haemangioglioblastoma
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11
Q

Phaeochromocytoma

Biochemical diagnosis

what scan can you do

A

24 hour urine

  • –Normetanephrines & Metanephrines
  • – 3 Methoxytyromine

Plasma

  • – Noradrenalin & Adrenalin
  • – Metanephrines

MIGB scan

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12
Q

Phaeochromocytoma

CATCHES
what else can elevate measured catecholamines

A

Obstructive Sleep Apnoea
Amphetamine like drugs
L-DOPA
Labetalol

Urine Dopamine comes from Kidney & Nervous system NOT the Adrenal Medulla. So measure urine Methoxytyramine

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13
Q

Phaeochromocytoma

management and aftercare

A

Alpha Blockers

  • –Phenoxybenzamine
  • –Doxazocin

Beta Blockers
—Propranolol

Laparoscopic adrenalectomy

POST ADRENALECTOMY
---Consider Genetic testing
30% are genetic ( 13 mutations so far)
---Annual Metanephrines: 24 hour urine, Plasma
---Additional treatment if Malignant
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