Heme/Onc Flashcards

1
Q

Management of acute chest

A

IVF, analgesics, incentive spirometry, antibiotics. If moderate ( sat >85% and less than or = 2 lobes involved) then transfuse PRBCs. If severe (sat <85% and more than 2 lobes involved) then do exchange transfusion

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2
Q

Secondary prophylaxis against strokes in patients with HbSS disease

A

Simple transfusions every 4-6 weeks wiht goal HbS < 30% and total Hb 9-12.5

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3
Q

Peripheral B cell count >5000 with CD5, ,CD19, CD20 and CD23 expression

A

CLL

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4
Q

Type of anemia that can be associated with CLL and is sometimes it’s presentation

A

Warm autoimmune hemolytic anemia

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5
Q

Patient with history of polycythemia vera who has no longer required transfusions and presents with hepatosplenomegaly and consitutional symptoms

A

Myelofibrosis

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6
Q

Things to consider in a patient with peripheral neuropathy, macrocytic anemia and diabetes

A

Metformin reduces intestinal absorption of B12 by at least 30%

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7
Q

Best treatment for solitary brain metastasis

A

Surgery or sterotactic radiation followed by whole brain radiation. Do chemo after treatment of brain mets as chemo has poor penetration of blood brain barrier

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8
Q

Dabigatran use and surgery planning

A

For planned surgery or non-emergent should wait 48 hours post last dose and then it will be cleared from system. If more emergent, can check thrombin time - if normal, not AC and can proceed. If elevated give idracizumab (antidote) and proceed

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9
Q

Constitutional symptoms, flank pain, erythrocytosis and microscopic hematuria

A

Renal Cell carcinoma

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10
Q

Elevated gamma gap with constitutional symptoms, and manifestations secondary to infiltration of hematopoietic tissue (hepatosplenomegaly and cytopenias) and excessive IgM in blood (sensorimotor peripheral neuropathy and hyperviscosity syndrome), can have “sausage link” retinal veins

A

Waldenstrom macoglobulinemia

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11
Q

In patients with bone metastases - how can you delay skeletal-related events (Fracture, skeletal instability/loss, spinal cord compression) and delay symptom onset

A

Osteoclast inhibiting agents (Denosumab and bisphosphonates).

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12
Q

Next step in evaluating a patient with prolonged PTT and normal PT.

A

Mixing study - this determines between inhibitor or factor deficiency. Deficiency will correct with mixing study, inhibitor will stay abnormal with mixing study

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13
Q

Management of mild bleeding or peri-op for minor procedures in patients with mild/moderate VWD

A

desmopressin

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14
Q

Management of severe bleeding episodes or invasive surgeries of those with VWD

A

VWF preparations

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15
Q

Weight loss, long smoking history, shoulder pain with paresthesias

A

consider superior pulmonary sulcus (pancoast) tumor

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16
Q

Clonal myeloproliferative disorder with proliferation of RBCs independent of Epo - thus Epo is typically LOW

A

Polycythemia vera

17
Q

Treatment in CML

A

Tyrosine kinase inhibitors (imatinib)

18
Q

Normocytic anemia, massive splenomegaly and tear drop cells with massive hepatosplenomegaly

A

Primary myelofibrosis