| WALDEN UNIVERSITY | 2025/2026 EDITION | 150+ VERIFIED
QUESTIONS WITH CORRECT, DETAILED ANSWERS AND
EXPLANATIONS
A 4-year-old child appears listless for the last week. He complains of pain when he
is picked up by his mother, and he is irritable when touching his arms or legs.
Several large ecchymotic lesions have appeared on his right thigh and left shoulder.
A complete blood count reveals a HgB=10.2, Hct=30.5%, MCV=96fL, platelet
count of 45,000/ML, and WBC count of 13,990/ML. Examination of the peripheral
blood smear reveals numerous blasts. The blasts lack peroxidase-positive granules
but do contain periodic acid-Schiff (PAS)-positive aggregates and stain positively
for TdT. Flow cytometry shows the phenotype of blasts to be CD19+, CD3-, and
sIg-. What is the most likely diagnosis?
A. Acute lymphoblastic leukemia (ALL)
B. Chronic lymphocytic leukemia (CLL)
C. Acute myelogenous leukemia (AML)
D. Chronic myelogenous leukemia (CML)
Acute lymphoblastic leukemia
A 55-year-old male had a fasting blood glucose level of 160 mg/dL 1 month ago.
Today, his fasting glucose level is 140 mg/dL. He has a history of HTN that is
controlled with an ACE inhibitor. He has no other medical problems. He is 5'11"
and weighs 215 lbs. His father had DM, but the family history is otherwise
noncontributory. This patient is asymptomatic, and his physical examination is
unremarkable. What is the most likely diagnosis?
A. Maturity Onset Diabetes of the Young (MODY)
B. Addison's disease
C. Type 2 Diabetes
D. Cushing's syndrome
C. type 2 diabetes
,A 13-year-old male has been drinking large quantities of fluids and has an
insatiable appetite, even for a teenager. However, he is losing weight and has
become more tired and listless over the past month. A complete blood count is
normal, but he is found to have a fasting serum glucose of 175 mg/dL. A diagnosis
of type 1 diabetes is made. What is the probable inheritance pattern of his
underlying disease?
A. Autosomal dominant
B. Multi-factorial
C. X-linked recessive
D. Autosomal recessive
B. Multifactorial
Ms. Jackson, a 45 y/o female, complains of fatigue, weight gain, lack of
concentration, and swelling for almost one year. The Nurse Practitioner thinks the
patient could have hypothyroidism based on her clinical presentation. Which lab
values would help to confirm Ms. Jackson's diagnosis of hypothyroidism?
A. Increased TSH and decreased free T4
B. Increased TSH and increased T3
C. Decreased TSH and increased total T4
D. Decreased TSH and decreased free T4
A. increased TSH and decreased free t4
Mr. Mann, age 50, presents to the Emergency Department with his wife for
complaints of palpitations, feeling of panic with shakiness, headache, nausea for
the past two hours. Upon arrival BP is 210/105. His medical history is significant
for GERD and HTN. He takes Prilosec OTC daily and lisinopril 10mg daily. He
has no known medication allergies. His family history includes HTN and
cardiovascular disease in father, osteoporosis, anxiety, and HTN in mother, and
breast cancer in only sister. His wife states the patient did this a couple of weeks
ago on two different occasions, but the symptoms went away in just one or two
minutes. His physical exam reveals mild diaphoresis, epigastric tenderness, and
generalized trembling. What diagnosis does this patient's presentation most closely
represent?
A. Myxedema Coma
B. Addison's Disease
,C. Thyrotoxicosis
D. Pheochromocytoma
D. pheochromocytoma
A 72-year-old male is brought to the ED in a coma. He was delivered to the ED
from a nursing home and was reported by the nursing home staff to have had a
seizure that lasted less than 1 minute. He was subsequently confused and soon
thereafter entered a comatose state. His medical history is significant for Type II
DM requiring insulin, HTN, and mild CHF. In the ED, the patient is very lethargic
and responds only to painful stimuli. His vital signs are stable. The list of
differential diagnoses that can cause seizure and coma. What is the most important
diagnostic study to do immediately?
A. Serum toxicology
B. CT head without contrast
C. CT head with contrast
D. Serum glucose
D. serum glucose
A 2-year-old child who recently immigrated to the United States has failure to
thrive. The child is short, with course facial features, a protruding tongue, and an
umbilical hernia. Profound mental retardation is apparent as the child matures.
These findings are best explained by a lack of:
A. Somatostatin
B. Cortisol
C. Thyroxine (T4)
D. Norepinephrine
C. thyroxine
A 3-year-old child of Italian ancestry presents with failure to thrive. Physical
examination indicates hepatosplenomegaly. His hemoglobin concentration is 6
g/dL, and the peripheral blood smear reveals severely hypochromic microcytic red
cells. Total serum iron level is normal. The reticulocyte count is 10%. Hemoglobin
electrophoresis shows very little hemoglobin A. A radiograph of the skull shows
maxillofacial deformities. What is the principle cause of anemia and other
abnormalities in this patient?
, A. Reduced synthesis of hemoglobin F
B. Reduced red blood cell survival from imbalance in the production of alpha and
beta globin chains
C. Relative deficiency of vitamin B12
D. Increased fragility of the erythrocyte membrane
Reduced synthesis of hemoglobin F
A 68-year-old previously healthy female has been feeling increasingly tired and
weak for several months. She states that she has had black, tarry stools for several
weeks. She is found to be anemic with a hemoglobin concentration of 9.3g/dL. The
peripheral blood smear reveals microcytic and hypochromic blood cells. Which of
the following conditions should be suspected as the most likely of her condition as
indicated by the peripheral blood smear?
A. Aplastic anemia
B. Beta thalassemia
C. Gastrointestinal blood loss
D. Pernicious anemia
Gastrointestinal blood loss
A 76-year-old female notices that small, pinpoint to blotchy areas of superficial
hemorrhage have appeared on her gums and on the skin of her arms and legs over
several weeks. She is found to have a normal prothrombin time (PT) and partial
thromboplastin time (PTT). Her CBC shows hemoglobin concentration of 12.7
g/dL, hematocrit of 37.2%. MCV of 80 fL/red cell, platelet count of
276,000/microliter, and WBC of 5600/microliter. Her template bleeding time is 3
minutes. Her fibrinogen level is normal, and there are no fibrin split products
detectable. Which of the following conditions best explain these findings?
A. Chronic renal failure
B. Macronodular cirrhosis
C. Vitamin B12 deficiency
D. Vitamin C deficiency