Adrenal Glands and the Pancreas Flashcards

1
Q

Describe features of primary hyperaldosteronism

A

Conn’s Syndrome - Renin levels are low, metabolic alkalosis and hypokalaemia. Aldosterone levels remain high and ignore negative feedback loop.
Most common cause is bilateral nodular hyperplasia. Less common is a small solitary aldosterone producing adenoma.

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2
Q

Describe features of secondary hyperaldosteronism

A

Renin is high. Can occur due to reduced renal perfusion

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3
Q

What is the mechanism involved in congenital adrenal hyperplasia?

A

21 hydroxylase deficiency or 11-beta hydroxylase deficiency,

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4
Q

Name some tumours of the endocrine pancreas

A
  • Tumours of Islet cells = Pancreatic neuroendocrine tumours.
  • Beta cells = insulinoma (recurrent hypos),
  • Alpha cells = Glucagonoma (diabetes symptoms + characteristic rash)
  • Delta cells = Somatostatinoma,
  • Gastrinoma
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5
Q

What are the mechanisms of damage in diabetes?

A
  1. Advanced glycation end products- non-enzymatic reaction between glucose and proteins which effects their structure.
  2. Sorbitol pathway - Cells of retina, kidney and nerves allow free transport of glucose in and out. Conversion of glucose to sorbitol which exerts osmotic pressure effect
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6
Q

What are some of the chronic complications of diabetes mellitus?

A
  • Accelerated atheroma which can cause MI, cerebrovascular disease.
  • Retinopathy,
  • Nephropathy,
  • Neuropathy
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7
Q

What causes of Cushing’s disease will you see low ACTH?

A
  • With chronic administration of glucocorticoids.

- Primary adrenal adenomas

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7
Q

What causes of Cushing’s disease will you see low ACTH?

A
  • With chronic administration of glucocorticoids.

- Primary adrenal adenomas

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8
Q

Describe features of adrenocortical adenomas

A
  • Often clinically silent (non-functioning)
  • If functioning then it can cause hyperaldosteronism or cushingoid features.
  • Mostly sporadic and low malignant potential so only resect if functional
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9
Q

What is phaeochromocytoma?

A

Tumour of chromaffin cells. Intermittently produces catecholamines.
Symptoms include hypertension, sweating, collapse and glycosuria.
Can be part of MEN

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10
Q

What are the causes of adrenal crisis?

A
  • Long term steroids can cause sepsis,
  • Rapid weaning/withdrawal of steroids,
  • Massive adrenal haemorrhage,
  • Infections such as meningococcal septicaemia,
  • Disseminated intravascular coagulation.
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11
Q

What are the features of primary adrenal insufficiency?

A

Addison’s Disease. Symptoms can be very non-specific but can present with low mood, unexplained nausea and vomiting, weight loss and constipation.
Most common cause is autoimmune but can be due to infection or metastatic cancers

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