Cushing Syndrome Quiz

Test your knowledge of the causes, symptoms, diagnosis, and treatment of Cushing syndrome, a condition caused by prolonged exposure to high levels of cortisol.

Question 1 / 10 0/10 answered (0 correct)
Topic: Endocrinology Difficulty: Intermediate

Cushing Syndrome: Practice Guide for Exam-Style Questions

Core Definition: Endogenous vs. Exogenous

Cushing syndrome is a clinical state resulting from chronic exposure to excess corticosteroids. It’s crucial to distinguish between its two main origins for diagnosis and treatment. Exogenous (iatrogenic) Cushing syndrome is the most common cause overall, resulting from long-term use of glucocorticoid medications. Endogenous Cushing syndrome is rarer and caused by the body’s own overproduction of cortisol.

Causes of Endogenous Cushing Syndrome

Endogenous causes are further divided into ACTH-dependent and ACTH-independent types. Understanding this division is key to answering questions about diagnostic workup.

  • ACTH-Dependent (80-85%): Excess ACTH from a tumor stimulates the adrenal glands. This is most commonly Cushing’s disease, caused by a pituitary adenoma. Less commonly, it’s from an ectopic ACTH-producing tumor (e.g., small cell lung cancer).
  • ACTH-Independent (15-20%): The adrenal glands themselves are the source of excess cortisol, typically from an adrenal adenoma, carcinoma, or hyperplasia. In these cases, pituitary ACTH production is suppressed.

Pathophysiology of Cortisol Excess

Cortisol, a glucocorticoid, affects nearly every system in the body. Its catabolic effects on protein lead to muscle wasting and thin skin. Its effects on fat metabolism cause the characteristic central fat redistribution. It also increases gluconeogenesis and insulin resistance, leading to hyperglycemia, and has mineralocorticoid effects that can cause hypertension and hypokalemia.

Classic Clinical Manifestations

Exam questions often present a patient with a classic constellation of symptoms. Recognizing these is the first step.

  • Central (truncal) obesity with slender extremities
  • A rounded, plethoric face (“moon facies”)
  • Fat accumulation on the upper back (“buffalo hump”)
  • Wide (>1 cm), purplish striae, typically on the abdomen
  • Proximal muscle weakness (difficulty standing from a chair)
  • Easy bruising and thin, fragile skin
  • Hypertension and hyperglycemia
Clinical Pearl: Don’t confuse Cushing’s syndrome with Cushing’s disease. Cushing’s syndrome is the general term for the condition of excess cortisol. Cushing’s disease is one specific cause: an ACTH-secreting pituitary adenoma. All patients with Cushing’s disease have Cushing’s syndrome, but not vice versa.

Diagnostic Screening Tests: The First Step

Initial testing aims to confirm the presence of hypercortisolism. Exam questions will test your knowledge of first-line screening options. At least one of the following is required:

  • 24-hour urinary free cortisol (UFC): Measures total cortisol excretion over a full day.
  • Late-night salivary cortisol: Cortisol levels should be lowest at night; elevated levels are suggestive.
  • Low-dose dexamethasone suppression test (LDDST): A healthy person’s cortisol will be suppressed by a small dose of dexamethasone; failure to suppress is abnormal.

Differentiating Cushing’s Disease from Ectopic ACTH

If a patient has ACTH-dependent Cushing syndrome, the next step is to find the source. The high-dose dexamethasone suppression test is a classic tool for this. Most pituitary adenomas (Cushing’s disease) will show some suppression of cortisol with a high dose of dexamethasone, whereas ectopic tumors typically do not.

Treatment Principles and Key Interventions

Treatment is directed at the underlying cause. For Cushing’s disease, the primary treatment is transsphenoidal surgery to remove the pituitary adenoma. For adrenal tumors, surgical resection is the standard. Medical therapy (e.g., ketoconazole, metyrapone) may be used to control cortisol levels before surgery or if surgery is not an option.

Key Takeaways

  • The most common cause of Cushing syndrome is iatrogenic (exogenous glucocorticoid use).
  • The most common endogenous cause is Cushing’s disease (an ACTH-secreting pituitary adenoma).
  • Diagnosis is a two-step process: first, confirm hypercortisolism, then determine the cause.
  • Plasma ACTH level is the critical test to differentiate between adrenal (low ACTH) and pituitary/ectopic (normal/high ACTH) causes.
  • Classic signs include central obesity, wide purple striae, moon facies, and proximal muscle weakness.

Frequently Asked Questions

What is the definitive difference between Cushing’s syndrome and Cushing’s disease?
Cushing’s syndrome is the collection of signs and symptoms caused by excess cortisol, regardless of the source. Cushing’s disease is a specific type of Cushing’s syndrome caused by an ACTH-producing tumor in the pituitary gland.
Why is a single morning plasma cortisol level not a good screening test?
Cortisol is secreted in a diurnal pattern and can fluctuate significantly due to stress. A single random or morning level is not reliable for diagnosing a chronic excess state. Tests that assess cortisol over time (24-hour urine) or at its nadir (late-night saliva) are more specific.
What is the purpose of the high-dose dexamethasone suppression test?
It helps differentiate between a pituitary source (Cushing’s disease) and an ectopic ACTH source in patients with ACTH-dependent Cushing syndrome. Pituitary adenomas often retain partial sensitivity and will suppress cortisol with high doses, while ectopic tumors usually do not.
How does an adrenal adenoma affect ACTH levels?
An adrenal adenoma produces cortisol autonomously. The resulting high levels of cortisol create strong negative feedback on the pituitary gland, suppressing its production of ACTH. Therefore, plasma ACTH will be very low or undetectable.
What are the most common metabolic complications?
Hyperglycemia (or overt diabetes mellitus) and insulin resistance are very common due to cortisol’s effect on glucose metabolism. Hypertension and hypokalemia (low potassium) are also frequent due to cortisol’s mineralocorticoid activity.
What is Nelson’s syndrome?
It is a rare but important complication that can occur after a patient with Cushing’s disease is treated with bilateral adrenalectomy. Removing the adrenal glands eliminates cortisol’s negative feedback, allowing the pituitary adenoma to grow aggressively, causing very high ACTH levels and mass effect symptoms.

This guide is for informational purposes and exam preparation only. It is not a substitute for professional medical advice, diagnosis, or treatment from a qualified healthcare provider.

PRO
Ad-Free Access
$3.99 / month
  • No Interruptions
  • Faster Page Loads
  • Support Content Creators