Hemato Flashcards

1
Q

…………… are the drugs of choice for stabilizing bony metastatic lesions to prevent hypercalcemia of malignancy and pathologic fractures.

A

Bisphosphonates (eg, zoledronic acid, pamidronate)

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2
Q

Anemia can be due to decreased red blood cell (RBC) production, increased RBC destruction, and frank blood loss.
lymphoproliferative disorders is due to

A

bone marrow infiltration with cancerous cells.

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3
Q

to 30% of patients on erythropoietin therapy develop new or worsening

A

hypertension,

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4
Q

Can help differentiate CML from leukemoid reaction

A

Leukocyte alkaline phosphatase (LAP) score

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5
Q

is diagnosed by flow cytometry (shov,ing a clonality of mature B cells)

A

CLL

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6
Q

is defined as treatment for a disease when standard therapy fails, such as radiation therapy for prostate-specific antigen recurrence after radical prostatectomy for prostate cancer

A

Salvage therapy

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7
Q

……… that target the 5HT3 receptor are considered first-line treatment for chemotherapy- induced nausea.

A

Serotonin (5HT) receptor antagonists (eg, ondansetron)

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8
Q

……… is the most common cause of inadequate respo nse to ESAs in patients on dialysis.

A

Iron deficiency

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9
Q

Risk factors for venous thromboembolism (VTE) are either

A

inherited (eg, Factor V Leiden, prothrombin gene mutation, protein C deficiency) or
acquired (eg, immobilization, surgery, malignancy, medications).

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10
Q

Febrile nonhemolytic transfusion reaction (FNHTR), the most common adverse transfusion reaction, is a benign occurrence caused by

A

cytokine release from leukocytes within the donor blood product.

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11
Q

Alcohol also directly hastens folate deficiency by

A

reducing folate absorption in the small intestine,
impairing uptake/storage in the liver,
and increasing urinary excretion.

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12
Q

Side effect of phenytoin

A

Folic acid deficiency
Gingival overgrowth/hyperplasia
reduced bone density

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13
Q

2nd most common of hereditary throbophelia in those of white ethnicity

A

Prothrombin mutation

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14
Q

Signs and symptoms of SVO include

A

dyspnea, venous congestion, and swelling of the head, neck and arms.

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15
Q

……… is the most commo n cause of SVC syndrome.

A

Malignancy

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16
Q

AIDS-defining malignancies such as

A

invasive cervical carcinoma (human papillomavirus),
Kaposi sarcoma (human herpesvirus 8),
CNS system lym phoma (Epstein-Barr virus [EBV]),
and NHL

17
Q

Patients with HIV are at significantly increased risk of malignancy due to immune dysregulation and reactivation of oncogenic viruses. One of the most common malignancies is non-Hodgkin lymphoma, which is due to the reactivation of the ……………

A

Epstein-Barr virus in B-lymphocytes.

18
Q

Most common of hereditary thrombophelia in those of white ethnicity

A

Factor V Leiden

19
Q

……… is the most commoly inherited hypercoagulable disorder in the Caucasian population, leading to increased risk of thrombosis.
Testing should be considered for an unprovoked first-time thrombus in young (age <45) patients or those with unusual site of thrombus.

A

Factor V Leiden

20
Q

In……… , leukocyte count, erythrocyte count, and coagu lation studies are normal

21
Q

………… often cause mild, asymptomatic hemolysis

A

Mechanical aortic valves

22
Q

chelates calcium and magnesium and may reduce their plasma leve ls, causing paresthesias.

23
Q

This patient most likely has hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome), an autosomal dominant disorder characterized by

A

diffuse telangiectasias (eg, ruby-colored papules that blanch v,ith pressure), recurrent epistaxis, and widespread arteriovenous malformations (AVMs).

24
Q

………… is the most common cancer in men and often presents with manifestations of metastatic disease

A

Prostate adenocarcinoma

25
Hemato logic abnorma lities occur in over half of SLE patients and include:
• Anemia, resulting from immune destruction, but also from coexisting renal disease or chronic inflammation • Leukopenia (eg, neutropenia), often immune-mediated and correlating with disease activity • Thrombocytopenia, most commonly due to immune thrombocytopenic purpura (ITP)
26
This patient is on isoniazid (INH), a pyridoxine (vitamin B6) antagonist that can cause acquired. ……… It frequently manifests as microcytic hypochromic anemia, simulating iron deficiency anemia.
sideroblastic anemia.
27
! ADAMTS13 level >>> uncleaved vWF multimers >>> platelet trapping & activation
TTP
28
Clinical features of TTP
• Hemolytic anemia (t LOH, ! haptoglobin) vv ith schistocytes • Thrombocytopen ia (t bleeding time, normal PT/PTT) • Renal failure • Neurologic manifestations • Fever
29
Management of TTP
Plasma exchange Glucocorticoids Rituximab
30
Patients with aggressive hematologic malignancies are at risk of tumor lysis syndrome when initiated on cytotoxic chemotherapy. Intrace llular contents are released, resulting in…………… Major complications include acute renal injury (uric acid/calcium phosphate tubular injury) and cardiac arrhythmias.
hyperuricemia, hyperkalemia, hyperphosphatemia, and hypoca lcemia (due to calcium phosphate binding).
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32
Vitamin B6, folate, and vitamin B12 are involved in the metabolism of homocysteine.………… lowers homocysteine levels by acting as a cofactor for the enzyme cystathionine 13 -synthase, vthich metabolizes homocysteine into cystathionine.
Vitamin B6
33
The ………… are the most common source of symptomatic pulmonary embo lism
proximal deep leg veins
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