lymphoid malignancies Flashcards

1
Q

acute lymphocytic leukemia characteristics

A

stem cell disorder
malignant proliferation
peak age 2-5 yoa

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2
Q

acute lymphocytic leukemia etiology

A

idiopathic
chromo ab (Downs syndrome)
leukemogenic factors

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3
Q

acute lymphocytic leukemia clinical course

A

abrupt onset
fatigue, pallor, weight loss, fever, bruising, bone pain

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4
Q

acute lymphocytic leukemia laboratory presentation

A

n/n anemia
thrombocytopenia
v wbc
diff: blasts (no auer rods)
cytochemistry: block + PAS
cell markers: CALLA, CD
classification: FAB
bm: hypercellular (increased blasts)

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5
Q

ALL TREATMENT

A

chemo/ radiation
bm transplant
umbilical cord treatment
80% survival in children

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6
Q

chronic lymphocytic leukemia laboratory presentation

A

n/n anemia
decreased plts
increased wbc
neutropenia
lymphocytosis
small lymphs
smudge cells

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7
Q

CML treatment

A

supportive
chemo/ radiation as needed

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8
Q

hairy cell leukemia characteristics

A

adult disease
male; female= 7:1

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9
Q

hairy cell leukemia clinical presentation

A

splengomegaly
increased infection

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10
Q

hairy cell leukemia laboratory presentation

A

pancytopenia
hairy cells
fibrosis in bm
TRAP stain +
immunophenotyping: B cells positive for CD 19, 20, 22, 25 etc.

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11
Q

hairy cell leukemia therapy

A

supportive
splenectomy
chemo

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12
Q

multiple myeloma charachteristics

A

adult median age 65
male predominance
malignant proliferation of plasma cells
monoclonal gammopathy (most IgG)

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13
Q

multiple myeloma clinical presentation

A

bone pain
lytic bone lesions and fractures
symptoms related to abnormalities

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14
Q

multiple myeloma laboratory presentation

A

increased plasma cells in bm
+/= plasma cells in peripheral blood
increased serium Ca
Bence Jones protein in urine
rouleaux
hazy smear
increased ESR
flame cells
ab. plasma cells with Dutcher bodies
immunophenotyping/ cytogenetics

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15
Q

multiple myeloma therapy

A

poor prognosis
chemo
bm/ stem cell transplant
death due to infection, fractures, renal failure

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16
Q

Waldenstrom’s Macroglobulnemia characteristics

A

malignant proliferation of plasma cells

17
Q

Waldenstrom’s Macroglobulinemia clinical/lab characteristics

A

lymphadenopathy
hepatosplenomegaly
monoclonal gammopathy (IgM)
hyperviscosity
NO bone lesions

18
Q

Waldenstrom’s Macroglobulinemia treatment

A

plasmapheresis: take unit of blood remove bad stuff give good back
median survival 4 yrs

19
Q

Sezary syndrome

A

T cell lymphoma

20
Q

Sezary Syndrome clinical/lab findings

A

erythrodema (skin infiltration and circulating Sezary cells)
sezary cell: t cell w/ irregular nuclear outline and fine chromatin (looks slightly immature)
treatment same as other lymphomas

21
Q

lymphomas characteristics

A

malignant neoplasm involving lymphoid organs
2 types: Hodgkins and Non Hodgkins
adult: peaks at 20-30/ >50 yoa
most common malignancy of young adults in US

22
Q

Hodgkin’s lymphoma characteristics

A

localized
central lymph nodes
contiguous spread
rare extra-nodal disease
peripheral blood not involved
bizarre cell apperance

23
Q

Non-Hodgkin’s lymphoma characteristics

A

widespread
peripheral lymph nodes
non-contiguous spread
extra-nodal disease common
peripheral blood may be involved
normal cell apperance (lymphs w/ clefts in nucleus but all look the same)

24
Q

lymphoma classification

A

based on cell types and spread of disease

25
Q

lymphoma treatment

A

chemo
radiation
2/3 hodgkin’s disease is curable- relapse possible

26
Q

Burkitt’s lymphoma

A

high incidence in Africa
often extra-nodal (facial bones, jaw, intestines, ovaries, kidney)
diagnosed by morphology and immunophenotyping (B cell in orgin)
typical cell= blue, vacuolated (L3) [big blue cells w/ vacuoles]
treatment: chemo