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NR-283 Exam 3: Pathophysiology V4 Updated and Latest Questions and Correct Answers with Rationale - Chamberlain University

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NR-283 Exam 3: Pathophysiology V4 Updated and Latest Questions and Correct Answers with Rationale - Chamberlain University

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NR-283 Exam 3: Pathophysiology V4 Updated and Latest
Questions and Correct Answers with Rationale -
Chamberlain University
1. Which clinical manifestation is a hallmark sign of Graves’ disease?


A. Exophthalmos


B. Weight gain and lethargy


C. Bradycardia


D. Cold intolerance



Ans: A


Rationale: Graves’ disease is an autoimmune condition leading to hyperthyroidism. It involves

antibodies that stimulate the TSH receptors constantly. Exophthalmos results from inflammation of the

extraocular muscles and fat. Patients often experience a high metabolic rate and heat intolerance.

Tachycardia is also a common cardiovascular finding in this disorder. Understanding these ocular

changes helps distinguish Graves’ from other thyroiditis types.

,2. A patient with Cushing’s syndrome is likely to demonstrate which of the following

findings?


A. Truncal obesity and moon face


B. Hyperpigmentation of the skin


C. Weight loss and dehydration


D. Hypoglycemia



Ans: A


Rationale: Cushing’s syndrome is caused by excessive levels of cortisol in the body. This

hypercortisolism leads to the redistribution of adipose tissue to the trunk. A moon face and buffalo hump

are classic physical indicators. Patients also commonly suffer from purple striae and thin skin.

Hyperglycemia is a frequent metabolic complication due to cortisol’s effects. Clinical assessment should

focus on these unique structural and metabolic shifts.


3. What is the primary cause of Type 1 Diabetes Mellitus?


A. Destruction of pancreatic beta cells


B. Excessive intake of dietary carbohydrates


C. Insulin resistance in peripheral tissues


D. Overproduction of glucagon by alpha cells



Ans: A


Rationale: Type 1 Diabetes Mellitus is primarily an autoimmune-mediated destruction process. The body

attacks its own pancreatic beta cells within the islets. This results in an absolute deficiency of insulin

,production. Patients must rely on exogenous insulin for survival and glucose control. It often presents

acutely with polyuria, polydipsia, and significant weight loss. Genetic and environmental factors both

play roles in the disease onset.


4. Which electrolyte imbalance is most commonly associated with SIADH?


A. Hypernatremia


B. Hypokalemia


C. Hyponatremia


D. Hypercalcemia



Ans: C


Rationale: SIADH involves the excessive release of antidiuretic hormone from the pituitary. This causes

the kidneys to reabsorb too much water. The excess water leads to dilutional hyponatremia in the blood.

Patients may exhibit symptoms ranging from confusion to seizures. Fluid restriction is often the primary

treatment for this condition. Monitoring serum sodium levels is critical for patient safety during care.


5. Which condition is characterized by a deficiency of ADH, leading to polyuria and dilute

urine?


A. Diabetes Mellitus


B. Diabetes Insipidus


C. SIADH


D. Cushing’s Disease



Ans: B

, Rationale: Diabetes Insipidus is caused by a lack of antidiuretic hormone. Without ADH, the kidneys

cannot concentrate urine effectively for the body. This results in the excretion of massive amounts of

dilute urine. Patients experience intense thirst and are at risk for dehydration. Hypernatremia is common

as the body loses free water rapidly. Treatment typically involves administering synthetic vasopressin to

replace the hormone.


6. A patient presents with hypotension, hyperkalemia, and skin hyperpigmentation. Which

disorder do you suspect?


A. Pheochromocytoma


B. Addison’s Disease


C. Conn’s Syndrome


D. Hashimoto’s Thyroiditis



Ans: B


Rationale: Addison’s disease occurs when the adrenal cortex fails to produce hormones. A deficiency in

cortisol and aldosterone leads to metabolic instability. High ACTH levels cause the characteristic bronze

hyperpigmentation of the skin. Hypotension and hyperkalemia result specifically from the lack of

aldosterone. This condition can lead to a life-threatening adrenal crisis if untreated. Lifelong hormone

replacement therapy is required for these patients.

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