WBC disorders Flashcards

(32 cards)

1
Q

Which leukemia is the most common cancer in children?

A

ALL (ages 3-7)

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2
Q

What are the features of all acute leukemias (ALL, AML)?

A

Sx of platelet problems (gingival bleeding, epistaxis, menorrhagia)

Sx of neutropenia (predisposed to infection)

Sx of anemia, thrombocytopenia, CN palsies, rash

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3
Q

What are the sx specific to younger patients (childhood to young adult) with acute leukemias?

A

fatigue, fever, lethargy, HA

bone/joint pain specific to sternum, tibia, femur

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4
Q

How do older patients present with acute leukemias?

A

Slow and progressive onset

lethargy, anorexia, dyspnea

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5
Q

With which acute leukemia do you find lymphadenopathy and hepatosplenomegaly?

A

ALL

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6
Q

What is a characteristic diagnostic finding of AML and ALL?

A

Increased WBCs; panycytopenia w/ blast cells

Bone marrow bx has blast cells

ALL: terminal deoxynucleotidyl

AML: Auer rods

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7
Q

How do you treat acute leukemias?

A

induction chemo with consolidation therapy (destroys leukemic cells)

2nd line: allogeneic bone marrow transplant

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8
Q

Which leukemia is the most prevalent?

A

CLL - malignancy of b lymphocytes

more common in males

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9
Q

What are the symptoms of CML?

A

Triphasic; gradual

Chronic: asymptomatic, may develop fatigue, anorexia, wt loss, fever, excess sweating

Accelerated: splenomegaly causes abd fullness, sx progress w/ bone pain and bruising

Acute “blast crisis”: very pronounced sx

Rarely may get blurred vision, resp distress, priapism

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10
Q

What is a pathognomonic dx of CML?

A

CBC shows leukocytosis

Also, 95% have Philadelphia chromosome mutation

Bone marrow bx shows left shift

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11
Q

How will you treat CML?

A

Allogeneic bone marrow transplant is curative!

Imatinib mesylate (Gleevec) for chronic phase

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12
Q

What is the outcome of CML?

A

80% survive

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13
Q

What are the symptoms of CLL?

A

indolent (painless)

peripheral lymphocytosis w/ invasion of bone marrow, liver, spleen, and lymph

recurrent infections, splenomegaly, lymphadenopathy

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14
Q

What is diagnostic of CLL?

A

CBC shows isolated lymphocytosis, leukocytosis

Periph smear shows smudge cells

Bone marrow bx has left shift

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15
Q

How do you treat CLL?

A

Mostly palliative care; resistant to tx

Can give chlorambucil PO or fludarabine IV

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16
Q

What is the outcome of CLL?

A

Median survival is 6 years :(

17
Q

In what population will you find Hodgkin lymphoma?

A

Ages 15-45 or over age 50

History of EBV (1/2 of cases)

18
Q

What are the symptoms of Hodgkin lymphoma?

A

painless cervical, supraclavic, and mediastinal lymphadenopathy

possible pain in node after ETOH

A sx: no constitutional sx

B sx: fever, wt loss, night sweats, pruritis, fatigue

19
Q

How are you going to dx Hodgkin lymphoma?

A
  1. r/o other reasons for lymphadenopathy
  2. lymph node bx
20
Q

What will you see in the lymph node bx for Hodgkin’s lymphoma?

A

Reed-Sternberg cells (look like owl eyes)

21
Q

How do you treat Hodgkin lymphoma?

A

Combination chemo

initial tx: radiation therapy

ABVD chemo

22
Q

Who gets Non-Hodgkin lymphoma?

A

Ages 20-40y

Risk with HIV, immudeficiency

23
Q

What are the 2 types of Non-Hodgkins lymphomas?

A

indolent (usually progress to…)

agressive

24
Q

What are the sx of non-hodgkins lymphoma?

A

isolated, painless lymphadenopathy, bone marrow may be involved

may migrate to extralymphatic sites

Burkitt lymphoma comes w/ abd fullness

less likely to have “B” sx

25
How do you diagnose non-hodgkin lymphoma?
1. r/o other causes of lymphadenopathy 2. Bx lymph nodes 3. establish staging by CXR, CT, bone marrow bx, LP
26
What will you find in lymph node bx of non-hodgkin lymphoma?
I have no effing idea, I just know that you do it.
27
How do you treat non-hodgkin lymphoma?
indolent: radiation therapy alone aggressive: chemo, immunotherapy, autologous stem cell transplantation
28
What exactly is multiple myeloma?
malignancy of plasma cells which produces abundant M protein
29
What are the symptoms of multiple myeloma?
anemia, bone pain (back/ribs), pathologic fx, infection rarely renal failure, spinal cord compression, hyperviscosity
30
What will you find on CBC and periph smear of multiple myeloma?
pancytopenic with normal cell morphology
31
What studies (other than CBC and smear) will you do for multiple myeloma?
Electrophoresis: **monoclonal spike** UA: **+ Bence Jones** protein Radiography: **"punched out"** regions
32
How do you treat multiple myeloma?
Refer to a specialist. Combo chemo, transplant, Biphosphonates as adjunt therapy.