Document 2026/2027 | Advanced Practice Nursing | 60 Verified Questions
with Detailed Rationales
SECTION 1: CELLULAR ADAPTATION AND INJURY (Questions 1-10)
Question 1
A patient with chronic hypertension develops left ventricular hypertrophy. Which type of
cellular adaptation is demonstrated?
A) Atrophy
B) Hypertrophy
C) Hyperplasia
D) Metaplasia
Correct Answer: B
Rationale: Hypertrophy is an increase in cell size that occurs when cells are subjected to
increased workload. In hypertension, the left ventricle works against increased afterload,
causing cardiac muscle cells to enlarge without increasing in number. This adaptation
increases contractile strength but can eventually become pathological.
Question 2
A patient who smokes develops squamous metaplasia in the bronchial epithelium. What is
the primary mechanism of metaplasia?
A) Increased cell size in response to workload
B) Increased cell number in response to hormonal stimulation
C) Replacement of one differentiated cell type with another in response to chronic
irritation
D) Decreased cell size due to reduced workload
Correct Answer: C
,Rationale: Metaplasia is the reversible replacement of one mature cell type by another less
mature cell type in response to chronic irritation or inflammation. In smokers, the normal
pseudostratified columnar epithelium is replaced by stratified squamous epithelium as a
protective response. This adaptation can predispose to malignant transformation.
Question 3
Which type of necrosis is characterized by the formation of a cheese-like (caseous)
appearance and is commonly associated with tuberculosis?
A) Coagulative necrosis
B) Liquefactive necrosis
C) Caseous necrosis
D) Fat necrosis
Correct Answer: C
Rationale: Caseous necrosis is a form of necrosis in which the dead tissue has a soft, friable,
cheese-like appearance. It is typically associated with granulomatous inflammation, most
commonly tuberculosis. The tissue appears amorphous with a white-yellow appearance.
Question 4
A patient experiences myocardial infarction. Which type of necrosis would the pathologist
observe in the affected cardiac tissue?
A) Liquefactive necrosis
B) Coagulative necrosis
C) Caseous necrosis
D) Fat necrosis
Correct Answer: B
Rationale: Coagulative necrosis is the characteristic type of necrosis in hypoxic injury, such
as myocardial infarction. The architecture of the dead tissue is preserved for several days
because the denatured proteins retain their shape. This is in contrast to liquefactive
necrosis (seen in brain infarcts) where tissue liquefies.
, Question 5
A patient with severe pancreatitis develops fat necrosis in the peritoneal cavity. What is
the mechanism of fat necrosis in pancreatitis?
A) Ischemia to adipose tissue
B) Bacterial infection of fat cells
C) Release of pancreatic lipases digesting fat tissue
D) Autoimmune destruction of adipocytes
Correct Answer: C
Rationale: In acute pancreatitis, pancreatic lipases are released into the peritoneal cavity
and digest adipose tissue, resulting in fat necrosis. The lipases break down triglycerides
into fatty acids, which combine with calcium to form calcium soaps (saponification). This
process can cause hypocalcemia in severe pancreatitis.
Question 6
What is the primary difference between necrosis and apoptosis?
A) Necrosis is programmed cell death; apoptosis is accidental
B) Necrosis is always pathological; apoptosis is always physiological
C) Necrosis is unregulated cell death causing inflammation; apoptosis is programmed cell
death without inflammation
D) Necrosis occurs only in cancer cells; apoptosis occurs only in healthy cells
Correct Answer: C
Rationale: Necrosis is unregulated, accidental cell death that typically triggers an
inflammatory response. Apoptosis is a highly regulated, programmed form of cell death
that occurs without inflammation. Apoptosis is essential for normal development and
tissue homeostasis.
Question 7
A patient with chronic obstructive pulmonary disease (COPD) develops atrophy of the
respiratory muscles. What is the primary mechanism of atrophy?
A) Increased protein synthesis
B) Decreased protein synthesis and increased protein degradation