Random Cancer Questions Flashcards

1
Q

cKIT mutation

A

Mastocytosis

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2
Q

t(9:22) p210

A

CML

Chronic Myelogenous Leukemia

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3
Q

Jak2 mutations are seen in which disorders? Name them

A

Myeloproliferative disorders

  1. Polycythemia Vera (RBCs)
  2. Essential Thrombocythemia (Platelets)
  3. Primary Myelofibrosis
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4
Q

Leukoerythroblastic change is seen in the peripheral smear of what myeloproliferative disorder?

What else will you see on it?

A

Primary Myelofibrosis

Also TEAR DROP RBCs, nucleated RBCs

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5
Q

Why is the spleen so f’ing huge in primary myelofibrosis?

A

Extramedullary hematopoiesis.

There is no room for it in the bone marrow so it moves to other sites in the body and spills blood cell precursors out into the peripheral circulation

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6
Q

What stain is used on the BM to ID Myelofibrosis?

A

Reticulin

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7
Q

Why does uric acid increase when you have high cell turnover?

A

The nuclei are released into the blood and uric acid gets out.

Clear it with ALLOPURINOL

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8
Q

Tx for Polycythemia Vera?

A

Venesection

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9
Q

Polycythemia Vera and Essential Thrombocythemia can transition to what 2 diseases?

A
  1. Primary Myelofibrosis (most common)

2. AML

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10
Q

AML has generalized bone marrow failure associated with its myeloid lineage proliferation. What are the characteristics of bone marrow failure?

A

Anemia - shortness of breath, chest pain, fatigue

Thrombocytopenia - bleeding

Neutropenia - INFECTION

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11
Q

Congenital form of Aplastic Anemia

A

Fanconi’s

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12
Q

Primary mechanism of idiopathic aplastic anemia?

A

Immune-mediated destruction of hematopoietic stem cells.

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13
Q

TEST: What causes Aplastic Anemia in Sickle Cell patients?

A

PARVOVIRUS

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14
Q

What lab results are characteristic of Aplastic Anemia?

A

Decreased Reticulocyte Count

HYPOCELLULAR MARROW

Relative lymphocytosis –> in other words, you have severe pancytopenia (RBCs, platelets, granulocytes) but your lymphocytes have longer lives, so it seems like lymphocytosis

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15
Q

What’s the main difference between aplastic anemia and a myelodysplastic syndrome?

A

They both have pancytopenia, impaired hematopoietic stem cells.

ONE IS NEOPLASTIC AND THE OTHER ISNT

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16
Q

Where do myelodysplasias lead? (uh oh….)

A

Acute Myelogenous Leukemia

17
Q

Treatment for Myelodysplasias?

A

“lidomides”

Thalidomide
Lenalidomide

SCT in younger patients

18
Q

TEST: Describe an Autologous Hematopoietic Stem Cell Transplant

A

Stem cells collected from patient’s peripheral blood and stored (very resilient)

Patient’s marrow wiped out with chemo, and stored cells injected back in.

Stem cells somehow find their way back to the bone marrow and set up camp.

19
Q

When do you usually use HSCT?

A

Multiple Myeloma/Lymphoma

20
Q

Can you do an Autologous HSCT in a patient with aplastic anemia or myeodysplasia?

A

NOPE their stem cells are screwed up. Have to do an Allogenic Hematopoietic Stem Cell Transplant

21
Q

Can a person with bone lytic lesions have MGUS?

A

Nope. Any indication of CRAB+ = multiple myeloma