A 74-year-old man returns to his physician to follow-up on laboratory studies obtained for anemia 2 weeks ago. He has no complaints. He has a 20-year history of hypertension and several years of knee osteoarthritis. He walks 2 miles a day. He does not smoke. He drinks alcohol moderately. He takes hydrochlorothiazide, losartan, and pain killers, including ibuprofen. The vital signs include: temperature 37.1°C (98.8°F), pulse 68/min, respiratory rate 12/min, and blood pressure 110/70 mm Hg. The physical examination shows no abnormalities. The laboratory studies show the following:
Laboratory test
Hemoglobin 10 g/dL
Mean corpuscular volume 75 μm3
Leukocyte count 5,000/mm3
Platelet count 350,000/mm3
ESR 18 mm/hr
Serum
Ferritin 5 μg/L
Iron 30 μg/L
Total iron-binding capacity 500 μg/dL
Calcium (Ca+) 9 mg/dL
Albumin 4 g/dL
Urea nitrogen 14 mg/dL
Creatinine 0.9 mg/dL
Monoclonal protein on serum electrophoresis is 12 g/L (non-IgM). Clonal bone marrow plasma cells comprise 4% of the total number of cells. Skeletal survey with magnetic resonance imaging reveals no pathologic findings. In addition to iron deficiency anemia, which of the following diagnosis is most appropriate to consider?
Q912
A 29-year-old woman comes to her primary care physician hoping she is pregnant. She reports that she had been taking oral contraceptive pills, but she stopped when she began trying to get pregnant about 7 months ago. Since then she has not had her period. She took a few home pregnancy tests that were negative, but she feels they could be wrong. She says she has gained 4 lbs in the past month, and her breasts feel full. Today, she expressed milk from her nipples. She complains of fatigue, which she attributes to stress at work, and headaches, to which she says “my sister told me she had headaches when she was pregnant.” She denies spotting or vaginal discharge. Her last menstrual period was at age 22, prior to starting oral contraceptive pills. Her medical and surgical history are non-significant. She has no history of sexually transmitted infections. She reports she and her husband are having intercourse 3-4 times a week. Her family history is significant for breast cancer in her mother and an aunt who died of ovarian cancer at 55. On physical examination, no breast masses are appreciated, but compression of the nipples produces whitish discharge bilaterally. A bimanual pelvic examination is normal. A urine pregnancy test is negative. Which of the following is the best initial step in management for this patient?
Q913
A 45-year-old woman presents to the office complaining of bilateral joint pain and stiffness in her hand joints for the past 3 months. She reports increasing difficulty holding a coffee cup or pen due to stiffness, especially in the morning. Over-the-counter ibuprofen partially relieves her symptoms. Past medical history is significant for dysthymia and gastroesophageal reflux disease. Vital signs are normal except for a low-grade fever. On examination, there is mild swelling and tenderness in the proximal interphalangeal and metacarpophalangeal joints and wrists. Nontender and non-pruritic nodules near the elbows are noted. Chest and abdominal examination are normal. X-rays of the hands reveal soft tissue swelling, joint space narrowing, and bony erosions. Her hematocrit is 32%, and her erythrocyte sedimentation rate is 40 mm/hr. This patient is at greatest risk for which of the following?
Q914
A 42-year-old man presents to the emergency department with persistent cough. The patient states that for the past week he has been coughing. He also states that he has seen blood in his sputum and experienced shortness of breath. On review of systems, the patient endorses fever and chills as well as joint pain. His temperature is 102°F (38.9°C), blood pressure is 159/98 mmHg, pulse is 80/min, respirations are 14/min, and oxygen saturation is 98% on room air. Laboratory values are ordered as seen below.
Hemoglobin: 12 g/dL
Hematocrit: 36%
Leukocyte count: 7,500/mm^3 with normal differential
Platelet count: 107,000/mm^3
Serum:
Na+: 138 mEq/L
Cl-: 101 mEq/L
K+: 4.2 mEq/L
HCO3-: 24 mEq/L
BUN: 32 mg/dL
Glucose: 99 mg/dL
Creatinine: 1.9 mg/dL
Ca2+: 10.0 mg/dL
AST: 11 U/L
ALT: 10 U/L
Urine:
Color: Amber, cloudy
Red blood cells: Positive
Protein: Positive
Which of the following is the best next step in management?
Q915
A 64-year-old woman presents to her primary care physician complaining of difficulty maintaining her balance while walking. Her husband comes along to the appointment with her, because he feels that she has not been acting herself at home lately. After further questioning him, it is noted that she has recently been voiding urine unintentionally at inappropriate times. If there is suspicion for an intracranial process, what would most likely be seen on MRI and what is the treatment?
Q916
A 52-year-old woman presents with fatigue and pain of the proximal interphalangeal and metacarpophalangeal joints for the past 6 months. She also has knee and wrist pain that has been present for the past 2 months, with morning stiffness that improves over the course of the day. Physical examination is significant for subcutaneous nodules. Laboratory tests are significant for the following:
Hemoglobin 12.5 g/dL
Red blood cell count 4.9 x 106/µL
White blood cell count 5,000/mm3
Platelet count 180,000/mm3
Coombs' test Negative
C-reactive peptide (CRP) Elevated
Erythrocyte sedimentation rate (ESR) Elevated
Anti-cyclic citrullinated peptide antibody (anti-CCP antibody) Moderately positive
Anti-nuclear antibody (ANA) Negative
Rheumatoid factor (RF) Negative
What is the most likely human leukocyte antigen (HLA) subtype associated with this disease?
Q917
A 27-year-old woman presents to the emergency department for sudden, bilateral, painful loss of vision. She states that her symptoms started last night and have persisted until this morning. The patient has a past medical history of peripheral neuropathy which is currently treated with duloxetine and severe anxiety. Her temperature is 99.5°F (37.5°C), blood pressure is 100/60 mmHg, pulse is 100/min, respirations are 15/min, and oxygen saturation is 98% on room air. On physical exam, the patient demonstrates 4/5 strength in her upper and lower extremities with decreased sensation in her fingers bilaterally. Towards the end of the exam, the patient embarrassingly admits to having an episode of urinary incontinence the previous night. An MRI is obtained and is within normal limits. Which of the following represents the best next diagnostic step and its most likely result for this patient?
Q918
A 70-year-old male patient comes into your office because of leg pain. The patient states that his calves have been hurting more and more over the last two months. The pain isn't present at rest, but the pain develops as the patient starts walking and exerting himself. He states that stopping to rest is the only thing that relieves the pain. Of note, the patient's medical history is significant for 30-pack-years of smoking, hypertension, hyperlipidemia, and a previous myocardial infarction status-post angioplasty and stent. On exam, the patient's lower legs (below knee) have glossy skin with loss of hair. The dorsalis pedis pulses are barely palpable bilaterally. Which of the following is the best initial therapy for this patient?
Q919
A 62-year-old man presents to the emergency department with increased fatigue and changes in his vision. The patient states that for the past month he has felt abnormally tired, and today he noticed his vision was blurry. The patient also endorses increased sweating at night and new onset headaches. He states that he currently feels dizzy. The patient has a past medical history of diabetes and hypertension. His current medications include insulin, metformin, and lisinopril. His temperature is 99.5°F (37.5°C), blood pressure is 157/98 mmHg, pulse is 90/min, respirations are 17/min, and oxygen saturation is 98% on room air. Cardiopulmonary exam is within normal limits. HEENT exam reveals non-tender posterior and anterior chain lymphadenopathy. Abdominal exam reveals splenomegaly and hepatomegaly. There are large, non-tender palpable lymph nodes in the patient's inguinal region. Neurological exam is notable for decreased sensation in the patient's hands and feet. He also complains of a numb/tingling pain in his extremities that has been persistent during this time. Dermatologic exam is notable for multiple bruises on his upper and lower extremities. Which of the following is most likely to be abnormal in this patient?
Q920
A 27-year-old woman presents to your office complaining of difficulty swallowing, and she describes that "there is something in the back of her throat". Furthermore, she also feels an "achy" chest pain that has been getting progressively worse over the last few weeks. She denies having any fever, shortness of breath, cough, abdominal pain, heartburn, nausea, or vomiting. The patient has a history of wrist fracture as a child, migraines, and a recent diagnosis of myasthenia gravis. Which of the following is the most likely diagnosis?
Cardiology US Medical PG Practice Questions and MCQs
Question 911: A 74-year-old man returns to his physician to follow-up on laboratory studies obtained for anemia 2 weeks ago. He has no complaints. He has a 20-year history of hypertension and several years of knee osteoarthritis. He walks 2 miles a day. He does not smoke. He drinks alcohol moderately. He takes hydrochlorothiazide, losartan, and pain killers, including ibuprofen. The vital signs include: temperature 37.1°C (98.8°F), pulse 68/min, respiratory rate 12/min, and blood pressure 110/70 mm Hg. The physical examination shows no abnormalities. The laboratory studies show the following:
Laboratory test
Hemoglobin 10 g/dL
Mean corpuscular volume 75 μm3
Leukocyte count 5,000/mm3
Platelet count 350,000/mm3
ESR 18 mm/hr
Serum
Ferritin 5 μg/L
Iron 30 μg/L
Total iron-binding capacity 500 μg/dL
Calcium (Ca+) 9 mg/dL
Albumin 4 g/dL
Urea nitrogen 14 mg/dL
Creatinine 0.9 mg/dL
Monoclonal protein on serum electrophoresis is 12 g/L (non-IgM). Clonal bone marrow plasma cells comprise 4% of the total number of cells. Skeletal survey with magnetic resonance imaging reveals no pathologic findings. In addition to iron deficiency anemia, which of the following diagnosis is most appropriate to consider?
A. Symptomatic multiple myeloma
B. Monoclonal gammopathy of undetermined significance (Correct Answer)
C. Waldenstrom’s macroglobulinemia
D. Solitary plasmacytoma
E. Smoldering (asymptomatic) multiple myeloma
Explanation: ***Monoclonal gammopathy of undetermined significance (MGUS)***
- The presence of **monoclonal protein <30 g/L** (12 g/L, non-IgM), **clonal bone marrow plasma cells <10%** (4% in this case), and **absence of CRAB criteria** (hypercalcemia, renal insufficiency, anemia, bone lesions) are classic diagnostic criteria for MGUS.
- The patient's **iron deficiency anemia** is unrelated to the plasma cell disorder and is likely secondary to chronic NSAID use (ibuprofen).
- MGUS requires monitoring but no treatment.
*Symptomatic multiple myeloma*
- Requires the presence of **CRAB criteria** (hypercalcemia, renal insufficiency, anemia related to myeloma, bone lesions) or **myeloma-defining events**, which are absent in this patient.
- Myeloma-related anemia is typically **normocytic/normochromic**, while this patient has **microcytic anemia due to iron deficiency**.
*Waldenstrom's macroglobulinemia*
- Characterized by **monoclonal IgM paraprotein** and lymphoplasmacytic lymphoma infiltration in the bone marrow.
- The patient's monoclonal protein is specifically stated as **non-IgM**, ruling out Waldenstrom's macroglobulinemia.
*Solitary plasmacytoma*
- Involves a **single solitary lesion** of clonal plasma cells in bone or soft tissue, with otherwise normal bone marrow (<10% plasma cells) and no CRAB criteria.
- The skeletal survey with MRI shows **no solitary lesion**, making this diagnosis inappropriate.
*Smoldering (asymptomatic) multiple myeloma*
- Defined by monoclonal protein **≥30 g/L** OR clonal bone marrow plasma cells **10-60%**, AND **absence of CRAB criteria or SLiM-CRAB criteria**.
- This patient's monoclonal protein is only **12 g/L** and bone marrow plasma cells are **4%**, both below the diagnostic thresholds for smoldering myeloma.
Question 912: A 29-year-old woman comes to her primary care physician hoping she is pregnant. She reports that she had been taking oral contraceptive pills, but she stopped when she began trying to get pregnant about 7 months ago. Since then she has not had her period. She took a few home pregnancy tests that were negative, but she feels they could be wrong. She says she has gained 4 lbs in the past month, and her breasts feel full. Today, she expressed milk from her nipples. She complains of fatigue, which she attributes to stress at work, and headaches, to which she says “my sister told me she had headaches when she was pregnant.” She denies spotting or vaginal discharge. Her last menstrual period was at age 22, prior to starting oral contraceptive pills. Her medical and surgical history are non-significant. She has no history of sexually transmitted infections. She reports she and her husband are having intercourse 3-4 times a week. Her family history is significant for breast cancer in her mother and an aunt who died of ovarian cancer at 55. On physical examination, no breast masses are appreciated, but compression of the nipples produces whitish discharge bilaterally. A bimanual pelvic examination is normal. A urine pregnancy test is negative. Which of the following is the best initial step in management for this patient?
A. Magnetic resonance imaging of the head
B. Pelvic ultrasound
C. Serum follicle-stimulating hormone/luteinizing hormone ratio
D. Serum thyroid-stimulating hormone level (Correct Answer)
E. Mammogram
Explanation: ***Serum thyroid-stimulating hormone level***
- The patient presents with **amenorrhea**, **galactorrhea**, and non-specific symptoms like **fatigue** and **headaches**. These symptoms can be indicative of **hypothyroidism**, which can cause hyperprolactinemia and subsequently lead to galactorrhea and menstrual irregularities due to its impact on the hypothalamic-pituitary-gonadal axis.
- **Thyroid-stimulating hormone (TSH)** is a crucial initial test as thyroid dysfunction is a common and treatable cause of these symptoms.
*Magnetic resonance imaging of the head*
- While **prolactinoma** causing hyperprolactinemia could lead to these symptoms and would eventually warrant an MRI, obtaining an MRI too early, before ruling out simpler and more common etiologies like hypothyroidism, is not the best initial step.
- An MRI would be indicated if **prolactin levels are elevated** and other causes, such as hypothyroidism, have been ruled out.
*Pelvic ultrasound*
- A pelvic ultrasound is primarily used to evaluate the **uterus and ovaries** for structural abnormalities.
- Given the patient's symptoms of **galactorrhea** and **amenorrhea** (without a positive pregnancy test), and the normal bimanual exam, a pelvic ultrasound is less likely to identify the primary cause compared to endocrine investigations.
*Serum follicle-stimulating hormone/luteinizing hormone ratio*
- This ratio is typically assessed in cases of **amenorrhea** to evaluate ovarian function or **polycystic ovary syndrome (PCOS)**.
- While relevant for amenorrhea, it does not directly address the prominent symptom of **galactorrhea** which points more towards a pituitary or thyroid issue.
*Mammogram*
- A mammogram is a screening tool for **breast cancer**, and while the patient has a family history, her current symptoms are related to **milk production (galactorrhea)** and **menstrual irregularities**, not suspicious breast masses.
- The physical exam showed no breast masses, and the discharge was bilateral and whitish, making breast cancer less likely as the primary cause of these specific symptoms.
Question 913: A 45-year-old woman presents to the office complaining of bilateral joint pain and stiffness in her hand joints for the past 3 months. She reports increasing difficulty holding a coffee cup or pen due to stiffness, especially in the morning. Over-the-counter ibuprofen partially relieves her symptoms. Past medical history is significant for dysthymia and gastroesophageal reflux disease. Vital signs are normal except for a low-grade fever. On examination, there is mild swelling and tenderness in the proximal interphalangeal and metacarpophalangeal joints and wrists. Nontender and non-pruritic nodules near the elbows are noted. Chest and abdominal examination are normal. X-rays of the hands reveal soft tissue swelling, joint space narrowing, and bony erosions. Her hematocrit is 32%, and her erythrocyte sedimentation rate is 40 mm/hr. This patient is at greatest risk for which of the following?
A. Obstructive pulmonary disease
B. Disease progression to distal interphalangeal joints
C. Sacroiliac joint inflammation
D. Osteitis deformans
E. Cardiovascular disease (Correct Answer)
Explanation: ***Cardiovascular disease***
- Patients with **rheumatoid arthritis (RA)**, suggested by the symptoms (bilateral hand joint pain, morning stiffness, swollen PIP/MCP joints, erosions, high ESR, subcutaneous nodules), have a significantly increased risk of **cardiovascular disease** due to systemic inflammation.
- Chronic inflammation accelerates **atherosclerosis**, leading to a higher incidence of myocardial infarction, stroke, and heart failure in RA patients.
*Obstructive pulmonary disease*
- While RA can cause **interstitial lung disease** (ILD), which is restrictive, it is not a primary risk factor for **obstructive pulmonary disease** like COPD unless the patient has a history of smoking.
- The presented symptoms do not directly point towards an obstructive lung process.
*Disease progression to distal interphalangeal joints*
- **Rheumatoid arthritis** typically spares the **distal interphalangeal (DIP) joints**, unlike **osteoarthritis** or **psoriatic arthritis**.
- Involvement of the DIP joints would suggest a different underlying rheumatologic condition.
*Sacroiliac joint inflammation*
- **Sacroiliac joint inflammation** (sacroiliitis) is a hallmark feature of **spondyloarthropathies** (e.g., ankylosing spondylitis), which are distinct from rheumatoid arthritis.
- RA primarily affects peripheral joints and typically does not involve the axial skeleton or sacroiliac joints.
*Osteitis deformans*
- **Osteitis deformans**, also known as **Paget's disease of bone**, is a chronic bone disorder characterized by abnormal bone remodeling.
- It is not directly related to or a common complication of rheumatoid arthritis nor do the symptoms suggest this condition.
Question 914: A 42-year-old man presents to the emergency department with persistent cough. The patient states that for the past week he has been coughing. He also states that he has seen blood in his sputum and experienced shortness of breath. On review of systems, the patient endorses fever and chills as well as joint pain. His temperature is 102°F (38.9°C), blood pressure is 159/98 mmHg, pulse is 80/min, respirations are 14/min, and oxygen saturation is 98% on room air. Laboratory values are ordered as seen below.
Hemoglobin: 12 g/dL
Hematocrit: 36%
Leukocyte count: 7,500/mm^3 with normal differential
Platelet count: 107,000/mm^3
Serum:
Na+: 138 mEq/L
Cl-: 101 mEq/L
K+: 4.2 mEq/L
HCO3-: 24 mEq/L
BUN: 32 mg/dL
Glucose: 99 mg/dL
Creatinine: 1.9 mg/dL
Ca2+: 10.0 mg/dL
AST: 11 U/L
ALT: 10 U/L
Urine:
Color: Amber, cloudy
Red blood cells: Positive
Protein: Positive
Which of the following is the best next step in management?
A. p-ANCA levels
B. Steroids
C. Azithromycin
D. Type IV collagen antibody levels (Correct Answer)
E. Renal biopsy
Explanation: ***Type IV collagen antibody levels***
- The patient presents with **pulmonary-renal syndrome**: hemoptysis, shortness of breath, elevated BUN/creatinine, hematuria, and proteinuria, which requires urgent evaluation for rapidly progressive glomerulonephritis (RPGN).
- **Anti-GBM antibodies** (type IV collagen antibodies) are diagnostic for **Goodpasture syndrome** (anti-GBM disease), which can present as life-threatening pulmonary hemorrhage and RPGN.
- While this patient has some **atypical features** for classic Goodpasture's (fever, arthralgias, thrombocytopenia suggest possible vasculitis), testing for **both anti-GBM and ANCA antibodies** is standard practice in pulmonary-renal syndrome.
- Anti-GBM disease requires **urgent diagnosis and treatment** (plasmapheresis + immunosuppression) to prevent irreversible renal failure.
*p-ANCA levels*
- **p-ANCA** is associated with **microscopic polyangiitis** and other ANCA-associated vasculitides, which can also present with pulmonary-renal syndrome.
- The constitutional symptoms (fever, arthralgias) and thrombocytopenia actually favor **ANCA-associated vasculitis** over Goodpasture's.
- In clinical practice, **both anti-GBM and ANCA antibodies should be sent simultaneously** when evaluating pulmonary-renal syndrome, as they guide different treatment approaches.
- This answer is reasonable but slightly less preferred in the context of this specific test question.
*Steroids*
- **Corticosteroids** are part of the treatment for both Goodpasture syndrome and ANCA-associated vasculitis.
- However, initiating empiric treatment before obtaining **diagnostic serology** is not ideal, as the diagnosis directs specific therapy (e.g., plasmapheresis for anti-GBM disease).
- In life-threatening presentations, steroids might be started empirically, but diagnostic testing should be done first or simultaneously.
*Azithromycin*
- **Azithromycin** is an antibiotic that would not address the underlying **autoimmune etiology** suggested by the pulmonary-renal syndrome.
- While infection should be in the differential with fever, the constellation of hemoptysis, glomerulonephritis, and systemic symptoms points to autoimmune disease.
*Renal biopsy*
- **Renal biopsy** is the gold standard for definitive diagnosis and would show **linear IgG deposition** along the glomerular basement membrane in Goodpasture syndrome.
- However, **serologic testing** (anti-GBM and ANCA antibodies) is **less invasive, faster, and highly specific**, making it the preferred initial diagnostic step.
- Biopsy may be pursued if serology is negative or equivocal, or to assess degree of renal damage and guide prognosis.
Question 915: A 64-year-old woman presents to her primary care physician complaining of difficulty maintaining her balance while walking. Her husband comes along to the appointment with her, because he feels that she has not been acting herself at home lately. After further questioning him, it is noted that she has recently been voiding urine unintentionally at inappropriate times. If there is suspicion for an intracranial process, what would most likely be seen on MRI and what is the treatment?
A. Constricted ventricles; surgical resection
B. Dilated ventricles; ventricular shunt (Correct Answer)
C. Constricted ventricles; watch and wait
D. Dilated ventricles; surgical resection
E. Constricted ventricles; ventricular shunt
Explanation: **Dilated ventricles; ventricular shunt**
- The patient's symptoms of **gait disturbance (difficulty maintaining balance)**, **cognitive decline (not acting herself)**, and **urinary incontinence** comprise the classic triad of **Normal Pressure Hydrocephalus (NPH)**.
- NPH is characterized by **ventriculomegaly (dilated ventricles)** on imaging, despite normal cerebrospinal fluid (CSF) pressure, and is often treated with a **ventriculoperitoneal (VP) shunt** to drain excess CSF.
*Constricted ventricles; surgical resection*
- **Constricted ventricles** would indicate a reduction in ventricular size, which is not consistent with the clinical presentation of NPH or other conditions causing increased intracranial pressure leading to these symptoms.
- **Surgical resection** is a treatment for tumors or other mass lesions, which would cause different symptom patterns and imaging findings; it is not a treatment for NPH.
*Constricted ventricles; watch and wait*
- As mentioned, **constricted ventricles** are not consistent with the clinical picture of NPH.
- A **"watch and wait"** approach would be inappropriate for NPH, as symptoms are progressive and often treatable with shunting.
*Dilated ventricles; surgical resection*
- While **dilated ventricles** are characteristic of NPH, **surgical resection** is incorrect as it is not the treatment for this condition.
- Surgical resection is primarily indicated for mass lesions and not for conditions involving CSF dynamics like NPH.
*Constricted ventricles; ventricular shunt*
- **Constricted ventricles** would rule out NPH, which is characterized by ventricular enlargement.
- A **ventricular shunt** is used to drain CSF from dilated ventricles, so this treatment would be inappropriate for constricted ventricles.
Question 916: A 52-year-old woman presents with fatigue and pain of the proximal interphalangeal and metacarpophalangeal joints for the past 6 months. She also has knee and wrist pain that has been present for the past 2 months, with morning stiffness that improves over the course of the day. Physical examination is significant for subcutaneous nodules. Laboratory tests are significant for the following:
Hemoglobin 12.5 g/dL
Red blood cell count 4.9 x 106/µL
White blood cell count 5,000/mm3
Platelet count 180,000/mm3
Coombs' test Negative
C-reactive peptide (CRP) Elevated
Erythrocyte sedimentation rate (ESR) Elevated
Anti-cyclic citrullinated peptide antibody (anti-CCP antibody) Moderately positive
Anti-nuclear antibody (ANA) Negative
Rheumatoid factor (RF) Negative
What is the most likely human leukocyte antigen (HLA) subtype associated with this disease?
A. HLA-B27
B. HLA-DR2
C. HLA-DQ2
D. HLA-DR4 (Correct Answer)
E. HLA-DR5
Explanation: ***HLA-DR4***
- The clinical presentation with **symmetrical polyarthritis** affecting small joints (PIP, MCP), morning stiffness, subcutaneous nodules, and elevated inflammatory markers (CRP, ESR) is highly suggestive of **rheumatoid arthritis (RA)**.
- **HLA-DR4** is the **most strongly associated HLA subtype with rheumatoid arthritis**, particularly in populations of European descent, and often correlates with more severe disease.
*HLA-B27*
- **HLA-B27** is primarily associated with **seronegative spondyloarthropathies**, such as ankylosing spondylitis, reactive arthritis, and psoriatic arthritis, which have different clinical features than those presented.
- The patient's symptoms (e.g., symmetrical small joint involvement, subcutaneous nodules) are inconsistent with the typical presentation of HLA-B27 associated diseases.
*HLA-DR2*
- **HLA-DR2** is associated with an increased risk of certain autoimmune diseases like **multiple sclerosis** and **narcolepsy**, but not primarily with rheumatoid arthritis.
- While some HLA alleles can have weak associations, DR2 is not a significant genetic marker for RA.
*HLA-DQ2*
- **HLA-DQ2** is strongly associated with **celiac disease** and, to a lesser extent, type 1 diabetes.
- There is no significant association between HLA-DQ2 and rheumatoid arthritis.
*HLA-DR5*
- **HLA-DR5** has been associated with certain autoimmune conditions such as **Hashimoto's thyroiditis** and some forms of uveitis.
- It is not a primary genetic risk factor for rheumatoid arthritis, especially when compared to HLA-DR4.
Question 917: A 27-year-old woman presents to the emergency department for sudden, bilateral, painful loss of vision. She states that her symptoms started last night and have persisted until this morning. The patient has a past medical history of peripheral neuropathy which is currently treated with duloxetine and severe anxiety. Her temperature is 99.5°F (37.5°C), blood pressure is 100/60 mmHg, pulse is 100/min, respirations are 15/min, and oxygen saturation is 98% on room air. On physical exam, the patient demonstrates 4/5 strength in her upper and lower extremities with decreased sensation in her fingers bilaterally. Towards the end of the exam, the patient embarrassingly admits to having an episode of urinary incontinence the previous night. An MRI is obtained and is within normal limits. Which of the following represents the best next diagnostic step and its most likely result for this patient?
A. A lumbar puncture demonstrating oligoclonal bands (Correct Answer)
B. Urine toxicology panel demonstrating cocaine use
C. A repeat MRI 3 days later demonstrating periventricular lesions
D. A psychiatric evaluation revealing multiple acute life stressors
E. A high resolution CT demonstrating hyperdense lesions
Explanation: **A lumbar puncture demonstrating oligoclonal bands**
- The patient's presentation with **sudden, bilateral, painful vision loss** (optic neuritis), **peripheral neuropathy**, **urinary incontinence**, and **fatigue** (implied by chronic anxiety and duloxetine use) is highly suggestive of **multiple sclerosis (MS)**.
- A **normal initial MRI** does not rule out MS, especially if the lesions are small or in areas difficult to visualize initially. **Oligoclonal bands** in the CSF are a classic finding in MS, indicating intrathecal immunoglobulin production.
*Urine toxicology panel demonstrating cocaine use*
- While cocaine can cause various neurological symptoms, it typically wouldn't present with this specific constellation of **optic neuritis**, **peripheral neuropathy**, and **urinary incontinence**.
- There are no direct indications in the patient's history or presentation (e.g., track marks, vasoconstriction) to strongly suspect cocaine use.
*A repeat MRI 3 days later demonstrating periventricular lesions*
- While a repeat MRI might eventually show lesions, especially considering the **dissemination in time and space** criteria for MS, waiting 3 days for MRI changes to appear isn't the *best next diagnostic step* given the acute symptoms.
- A lumbar puncture can provide immediate biochemical evidence (oligoclonal bands) that would support an MS diagnosis even with no initial MRI findings, or equivocal MRI findings, which would lead to earlier treatment.
*A psychiatric evaluation revealing multiple acute life stressors*
- While the patient has a history of **severe anxiety** and takes duloxetine (an antidepressant), her symptoms (optic neuritis, neuropathy, incontinence) are **neurological deficits** that cannot be solely attributed to psychological factors.
- While a psychiatric evaluation might be part of comprehensive care, it is not the *best next diagnostic step* to explain acute neurological symptoms.
*A high resolution CT demonstrating hyperdense lesions*
- **CT scans** are generally not the preferred imaging modality for early detection of MS lesions, as they are less sensitive than MRI for visualizing white matter plaques.
- **Hyperdense lesions** on CT typically indicate hemorrhage or calcification, which is not consistent with the likely etiology of the patient's symptoms.
Question 918: A 70-year-old male patient comes into your office because of leg pain. The patient states that his calves have been hurting more and more over the last two months. The pain isn't present at rest, but the pain develops as the patient starts walking and exerting himself. He states that stopping to rest is the only thing that relieves the pain. Of note, the patient's medical history is significant for 30-pack-years of smoking, hypertension, hyperlipidemia, and a previous myocardial infarction status-post angioplasty and stent. On exam, the patient's lower legs (below knee) have glossy skin with loss of hair. The dorsalis pedis pulses are barely palpable bilaterally. Which of the following is the best initial therapy for this patient?
A. Cilostazol
B. Angioplasty and stenting
C. Clopidogrel
D. Arterial bypass surgery
E. Lifestyle modifications (Correct Answer)
Explanation: ***Lifestyle modifications***
- **Lifestyle modifications**, particularly **smoking cessation** and a supervised **exercise program**, are the cornerstone of initial therapy for **peripheral artery disease (PAD)**, especially in patients with intermittent claudication.
- These interventions aim to improve collateral circulation, reduce cardiovascular risk, and improve exercise tolerance.
*Cilostazol*
- **Cilostazol** is a phosphodiesterase inhibitor used to treat **intermittent claudication** by improving blood flow and reducing symptoms.
- However, it is typically reserved for patients whose symptoms do not improve with initial **lifestyle modifications**, making it a second-line therapy.
*Angioplasty and stenting*
- **Angioplasty and stenting** are **revascularization procedures** indicated for patients with more severe PAD or those whose claudication is refractory to conservative management and significantly impacts their quality of life.
- They are not considered the best initial therapy, especially since the patient's symptoms, while bothersome, do not suggest immediate limb-threatening ischemia.
*Clopidogrel*
- **Clopidogrel** is an **antiplatelet medication** mainly used to reduce the risk of cardiovascular events (like MI or stroke) in patients with established **atherosclerotic disease**, including PAD.
- While important for secondary prevention, it does not directly address the symptoms of intermittent claudication as effectively as exercise or cilostazol.
*Arterial bypass surgery*
- **Arterial bypass surgery** is a major **revascularization procedure** generally reserved for patients with **severe PAD**, critical limb ischemia (e.g., rest pain, non-healing ulcers, gangrene), or extensive arterial occlusions that are not amenable to less invasive interventions.
- It carries significant risks and is not an appropriate initial treatment for this patient's presentation of intermittent claudication.
Question 919: A 62-year-old man presents to the emergency department with increased fatigue and changes in his vision. The patient states that for the past month he has felt abnormally tired, and today he noticed his vision was blurry. The patient also endorses increased sweating at night and new onset headaches. He states that he currently feels dizzy. The patient has a past medical history of diabetes and hypertension. His current medications include insulin, metformin, and lisinopril. His temperature is 99.5°F (37.5°C), blood pressure is 157/98 mmHg, pulse is 90/min, respirations are 17/min, and oxygen saturation is 98% on room air. Cardiopulmonary exam is within normal limits. HEENT exam reveals non-tender posterior and anterior chain lymphadenopathy. Abdominal exam reveals splenomegaly and hepatomegaly. There are large, non-tender palpable lymph nodes in the patient's inguinal region. Neurological exam is notable for decreased sensation in the patient's hands and feet. He also complains of a numb/tingling pain in his extremities that has been persistent during this time. Dermatologic exam is notable for multiple bruises on his upper and lower extremities. Which of the following is most likely to be abnormal in this patient?
A. Calcium
B. IgA and IgG
C. IgM (Correct Answer)
D. Natural killer cells
E. T-cells
Explanation: ***IgM***
- The patient's symptoms, including **fatigue**, **vision changes (blurry vision)**, **night sweats**, **headaches**, **dizziness**, **lymphadenopathy**, **hepatosplenomegaly**, **peripheral neuropathy** (decreased sensation, numb/tingling pain), and **easy bruising**, are highly suggestive of **Waldenström macroglobulinemia (WM)**.
- WM is a **B-cell lymphoma** characterized by the overproduction of **monoclonal IgM paraprotein**, which can lead to **hyperviscosity syndrome** (causing vision changes, headaches, dizziness) and other systemic symptoms.
*Calcium*
- While hypercalcemia can be seen in some hematologic malignancies, it is **not a typical feature of Waldenström macroglobulinemia**.
- **Multiple myeloma**, another plasma cell dyscrasia, is more commonly associated with hypercalcemia due to increased osteoclastic activity.
*IgA and IgG*
- **IgA and IgG myelomas** involve the overproduction of IgA and IgG antibodies, respectively, and present with different clinical features than described.
- The constellation of symptoms in this patient, particularly the signs of hyperviscosity and a B-cell lymphoma affecting IgM production, does not align with these types of immunoglobulin abnormalities.
*Natural killer cells*
- Abnormalities in **natural killer (NK) cells** are typically associated with certain viral infections, autoimmune diseases, or specific NK cell lymphomas, which do not match the clinical picture.
- While NK cells are part of the immune system, their primary role or dysfunction is not directly implicated in the presenting symptoms of Waldenström macroglobulinemia.
*T-cells*
- **T-cell lymphomas** involve the abnormal proliferation of T-lymphocytes and generally present with different clinical manifestations, such as skin lesions, lymphadenopathy, and organ infiltration.
- The systemic symptoms, hyperviscosity, and specific organ involvement noted in this patient are more characteristic of a B-cell malignancy like Waldenström macroglobulinemia, not a primary T-cell disorder.
Question 920: A 27-year-old woman presents to your office complaining of difficulty swallowing, and she describes that "there is something in the back of her throat". Furthermore, she also feels an "achy" chest pain that has been getting progressively worse over the last few weeks. She denies having any fever, shortness of breath, cough, abdominal pain, heartburn, nausea, or vomiting. The patient has a history of wrist fracture as a child, migraines, and a recent diagnosis of myasthenia gravis. Which of the following is the most likely diagnosis?
A. Mediastinitis
B. Superior vena cava syndrome
C. Benign tumor of the thymus (Correct Answer)
D. Thyroglossal duct cyst
E. Anaplastic thyroid cancer
Explanation: ***Benign tumor of the thymus***
- The patient's history of **myasthenia gravis** is strongly associated with **thymic abnormalities**, including benign thymomas, which can cause symptoms like difficulty swallowing and chest pain by compressing surrounding structures.
- The absence of fever, cough, or significant systemic symptoms makes infectious or more aggressive malignant processes less likely.
*Mediastinitis*
- This is an **inflammation of the mediastinum**, often accompanied by severe systemic symptoms such as **fever**, **chills**, and **profound malaise**, which are absent in this patient.
- It usually follows chest trauma, surgery, or esophageal rupture and would present acutely with more severe, diffuse pain rather than localized esophageal symptoms.
*Superior vena cava syndrome*
- This syndrome is characterized by **venous congestion** of the head, neck, and upper extremities, leading to **facial swelling**, **dyspnea**, and possibly **distended neck veins**.
- While it can cause chest discomfort, the primary symptoms presented (difficulty swallowing, foreign body sensation in the throat) are not typical of SVCS.
*Thyroglossal duct cyst*
- A thyroglossal duct cyst most commonly presents as a **midline neck mass** that moves with tongue protrusion.
- Although it can cause dysphagia if very large, it does not typically cause chest pain or have a direct association with myasthenia gravis.
*Anaplastic thyroid cancer*
- This is a highly aggressive thyroid malignancy that usually presents with a **rapidly enlarging neck mass**, hoarseness, and significant airway obstruction.
- It is typically seen in older individuals and would likely present with more acute and severe local compressive symptoms, including respiratory distress.