Internal Medicine Essentials Questions: Hematology Flashcards

1
Q

What labs suggest iron-deficiency anemia combined with anemia of chronic disease?

A
  • Normal ferritin and TIBC
  • Low iron

Ferritin is an acute phase reactant and as such cannot be relied on to diagnose iron-deficiency in someone with chronic inflammation (like RA).

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2
Q

A patient has elevated MCV and B12 in the low-normal range. Next step?

A

Test homocysteine and methylmalonic acid

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3
Q

Labs show decreased MCV, increased RDW, and platelets of 625,000. What is the likely diagnosis?

A

Iron-deficiency anemia

IDA can cause transient thrombocytosis. Correcting with oral ferrous sulfate will usually correct the elevation.

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4
Q

IV iron is reserved for those who ___________.

A

cannot tolerate oral iron

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5
Q

Which sickle cell patients should be given prophylactic penicillin?

A

Those 5 and younger

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6
Q

Those with HIT are at increased risk of _______________.

A

additional DVT

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7
Q

Therapy for ITP is usually reserved for ______________.

A

those with platelets less than 30,000 or those with bleeding symptoms; otherwise, weekly CBCs and observation are recommended

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8
Q

Describe the treatment protocol for polycythemia vera.

A
  • Aspirin
  • Phlebotomy to Hgb less than 45%
  • Hydroxyurea for those older than 60 or with thrombosis risk factors
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9
Q

Explain the diagnostic protocol for myelodysplastic syndrome.

A
  • Background: MDS is a disorder of bone marrow production. It will lead to decreased production of all hematopoietic cell lines, so symptoms include fatigue (anemia), infections (neutropenia), and easy bleeding (thrombocytopenia).
  • Diagnosis: CBC showing pancytopenia with evidence of dysplasia such as nucleated RBCs or hypogranular myelocytes.
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10
Q

What lab finding is diagnostic of leukemoid reactions?

A

Leukocytosis (exceeding 50,000) due to early neutrophils

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11
Q

Some risk factors for development of myelodysplastic syndrome include __________________.

A

radiation therapy and chemotherapy

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12
Q

Patients with MDS should be treated with ____________ to delay transition to AML.

A

azacitidine

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13
Q

A person with elevated serum protein, elevated IgG, and no symptoms likely has _________________.

A

monoclonal gammopathy of unknown significance (MGUS)

Note: you must distinguish this diagnosis from (1) smoldering multiple myeloma (which would be the same presentation but with IgG greater than 3 g/dL) and (2) amyloidosis (which would be this presentation but with symptoms of neuropathy, cardiomyopathy, and hepatomegaly).

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14
Q

List the ways to diagnose multiple myeloma.

A
  • Bone marrow biopsy showing greater than 10% plasma cells
  • Serum electrophoresis demonstrating M protein
  • Urine immunofixation of M protein

Note: some multiple myelomas may not have hypergammaglobulinemia.

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15
Q

Why is hypercalcemia in the presence of kidney failure a specific sign for multiple myeloma?

A

Kidney failure usually causes hypocalcemia because of hyperphosphatemia and decreased vitamin D synthesis.

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16
Q

Other than elevations in BUN and creatinine, what might you notice in the BMP of someone with multiple myeloma?

A

Decreased anion gap

17
Q

When you have a strong suspicion of von Willebrand factor deficiency, the most appropriate first test is _____________.

A

CBC followed by vWF antigen studies

18
Q

What is the accepted way of screening for bleeding disorders prior to elective surgery?

A

Clinical history

In the absence of episodes of unusual bleeding, bleeding disorders are highly unlikely.

19
Q

List the three most common scenarios in which DIC arises.

A
  • Infection
  • Cancer
  • Pregnancy
20
Q

Differentiate primary versus secondary hemostasis.

A
  • Primary: platelets

* Secondary: clotting factor

21
Q

When you suspect hemophilia, the best first test is _______________.

A

measurement of factors VIII and IX

22
Q

Thrombotic events can alter the levels of which proteins that may be causing thrombophilia?

A
  • Protein C
  • Protein S
  • Antithrombin

With these proteins, you need to wait until two weeks after warfarin treatment for a clot to measure for possible abnormalities.