Malignant Heme Disorders Flashcards

1
Q

patient presents with painless lymph node swelling, fever, night sweats, weight loss, pruritis. the lymphadenopathy arose in a single lymph node that spread, commonly starting in the cervical and supraclavicular regions. Dx?

A

hodgkin lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what 2 diagnostics help to diagnose hodgkin lymphoma?

A

PET/CT chest, abdomen, pelvis
lymph node open biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what finding in lymph node open biopsy indicates hodgkin lymphoma?

A

reed-sternberg cells (large, abnormal lymphocytes with more than 1 nucleus)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

patient presents with painless swollen anterior cervical lymph nodes, they have fever, night sweats, weight loss, abdominal pain/fullness and obstruction, and enlarged facial bones/thyroid/tonsils. Dx?

A

non-hodgkin lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what diagnostic is required to diagnose non-hodgkin lymphoma?

A

lymph node biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what finding in lymph node biopsy indicates non-hodgkin lymphoma?

A

malignant lymphoid cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is the mainstay treatment for non-hodgkin lymphoma?

A

chemotherapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

malignant proliferation of plasma cells originating in the bone marrow, producing excessive amounts of abnormal immunoglobins/light chains.

A

multiple myeloma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what class of immunoglobulin is most commonly associated with multiple myeloma?

A

IgG

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

in which patients does multiple myeloma occur in?

A

older adults

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

patient presents with bone pain in the hips/spine/ribs, history of osteolytic bones lesions/pathologic fractures, has S&S of anemia, and mucosal bleeding, visual changes, and infections. Dx?

A

multiple myeloma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what mnemonic helps us diagnose multiple myeloma?

A

CRAB

Calcium elevation
Renal Insufficiency
Anemia (normochromic/normocytic + rouleaux formations)
Bone disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what will urinalysis show to indicate multiple myeloma?

A

bence jones proteins (M or light chain proteins)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

stacking of RBCs due to abnormal albumin : globulin ratio.
what is it associated with?

A

rouleaux formation

multiple myeloma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is the diagnostic required to diagnose multiple myeloma?

A

bone marrow biopsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what is the treatment for multiple myeloma? (4)

A

induction therapy (choose 1):
lenalidomide / bortezomib

dexamethasone

chemotherapy
aggressive hydration
bisphosphonates

17
Q

what is the most common childhood malignancy that is a malignant proliferation of immune lymphoid stem cells in the bone marrow?

A

acute lymphoblastic leukemia (ALL)

18
Q

in which patients does acute lymphoblastic leukemia occur? (2)

A

4-5 yo
> 50 yo

19
Q

patient presents with history of being ill for days/weeks, petechiae, purpura, anemia findings, bone pain/arthralgias, headache, stiff neck, lymphadenopathy, cranial nerve palsies, and frequent infections. Dx?

A

acute lymphoblastic leukemia

20
Q

CBC reveals anemia, normal to slightly increased leukemic blast cells, and bone marrow biopsy is hypercellular with over 30% of them being lymphoblasts. Dx?

A

acute lymphoblastic leukemia

21
Q

WBC with a very large nucleus

A

blast cells

22
Q

what is the treatment for acute lymphoblastic leukemia?

A

intrathecal chemotherapy / cranial irradiation
maintenance chemo for 2-3 years

23
Q

what is the treatment for acute lymphoblastic leukemia that has relapsed?

A

bone marrow transplant

24
Q

most common in adults that is caused by proliferation of mature appearing lymphocytes in peripheral blood that invade the bone marrow, spleen, or lymph nodes.

A

chronic lymphoblastic leukemia

25
Q

patient presents with lymphadenopathy, splenomegaly, and leukemia cutis (flesh-colored-to-violaceous papules/plaques/nodules). Dx?

A

chronic lymphoblastic leukemia

26
Q

CBC reveals lymphocytosis, elevated WBC > 20,000, and peripheral blood smear reveals mature-appearing lymphocytes and smudge cells.

A

chronic lymphocytic leukemia

27
Q

remnants of cells that lack any identifiable cytoplasmic membrane or nuclear structure; AKA basket cells

A

smudge cells

28
Q

what is the treatment for chronic lymphoblastic leukemia if we decide to treat based on clinical indicators? (3)

A

chemotherapy
local radiation for painful lymphadenopathy
+/- transplant

29
Q

most common leukemia in adults that is caused by proliferation of abnormal myeloid cells that do not mature and affects WBCs, RBCs, and platelets.

A

acute myeloid leukemia

30
Q

patient presents with history of feeling ill for days, anemia findings, recurrent infections, bone pain, gingival hypertrophy, and leukemia cutis. Dx?

A

acute myeloid leukemia

31
Q

myeloblasts are present in BM or PBS, auer rods are on peripheral smear; myeloblasts are generally positive for peroxidase and sudan black histochemical stains. Dx?

A

acute myeloid leukemia

32
Q

what is the mainstay of treatment for acute myeloid leukemia? 2nd line treatment?

A

chemotherapy

allogenic bone marrow transplant

33
Q

caused by development of an abnormal chromosome called Philadelphia chromosome; proliferation of myeloid cells retain their capacity to differentiate/mature.

A

chronic myeloid leukemia

34
Q

CBC reveals elevated WBCs, increased granulocytes in all stages of maturity, thrombocytosis, and positive Philadelphia chromosome. Dx?

A

chronic myeloid leukemia

35
Q

what is the hallmark diagnostic finding for chronic myeloid leukemia?

A

BCR / ABL gene in peripheral blood smear or bone marrow biopsy

36
Q

what is the mainstay of treatment for chronic myeloid leukemia? what is the only proven curative therapy?

A

chemotherapy

allogenic bone marrow transplant