Lymphomas and Plasma cell disorders Flashcards

1
Q

Focus on B-cell proliferation

A

Lymph node Cortex

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2
Q

B lymphs and plasma cells

A

Lymph node Medulla

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3
Q

Contains T cells and macrophages

A

Lymph node paracortex

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4
Q

CD19, CD20, CD5

A

Naive B lymph CD markers

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5
Q

CD3, CD5, CD2, CD7, CD4, and CD8

A

T cell CD markers

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6
Q
  • Formation of new B lymphocytes
  • Processing of specific immunoglobulins
  • Filtration of matter, debris, and bacteria
A

Lymph node functions

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7
Q

In the pathology laboratory (moist)
- sliced into 3 mm-thick sections
-touch imprints
- thin sections

A

Lymph node processing

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8
Q

Morphology
Immunophenotype
Molecular Characteristics
Clinical Characteristics

A

Lymphoma subtypes are distinguished by…

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9
Q

Abnormal, destructive lymph node enlargement

A

Lymphoma characteristic

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10
Q

Progression into a leukemia

A

Peripheralization

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11
Q
  1. Mature B cell lymphoma
  2. Mature T cell lymphoma
A

Lymphoma categories

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12
Q

Reed sternberg cell

A

Hodgkin’s lymphoma

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13
Q

More common in kids

A

Hodgkin’s lymphoma

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14
Q

Happens to ALL ages

A

Non-Hodgkins Lymphoma

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15
Q

Unifocal origin with predictable spread along lymph node chain

A

Hodgkins

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16
Q

Presents with painless, englarged cervical lymph nodes

A

Hodgkins

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17
Q

Prognosis good if still localized (>90% cure)

A

Hodgkin’s lymphoma (HL)

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18
Q

Multifocal origin with unpredictable spread

A

Non-Hodgkins Lymphoma (NHL)

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19
Q

Malignant cell is B lymph in 95% of cases

A

Non-Hodgkins Lymphoma (NHL)

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20
Q

“owl-eyes”

A

Reed- Sternberg cell

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21
Q

Accurate staging crucial to treatment

A

Hodgkin’s lymphoma (HL)

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22
Q

Staging not as crucial

A

Non-Hodgkins Lymphoma (NHL)

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23
Q

Pleomorphic cells, some normal, some malignant

A

Hodgkin’s lymphoma (HL)

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24
Q

Uniform, malignant cells

A

Non-Hodgkins Lymphoma (NHL)

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25
Presents with painless, enlarged cervical lymph nodes & at a more advanced stage
Non-Hodgkins Lymphoma (NHL)
26
Prognosis worse
Non-Hodgkins Lymphoma (NHL)
27
fever, weight loss, night sweats (poor prognostic indicator)
B-symptoms
28
Popcorn cells
Nodular lymphocyte-Predominant Hodgkin Lymphoma (NLPHL)
29
Cells are positive for CD20 and CD45
Nodular lymphocyte-Predominant Hodgkin Lymphoma (NLPHL)
30
strong association w/ cmyc proto-oncogene rearrangement on chromosome 8
Non-Hodgkin’s Lymphoma (NHL)
31
NHL typically_____ have a leukemic presentation at the end stage of the disease
does
32
Essential to accurately stage disease to determine treatment and prognosis!
Diagnosis of HL
33
Radiation and chemo. Can affect 90% cure rate if disease is localized!
Hodgkins treatment
34
slow-growing
Low grade NHL
35
extranodal disease
Intermediate grade NHL
36
rapidly growing - rapidly fatal
High grade NHL
37
ranks according to aggressivity: low, intermediate or high grade
NHL (1982)
38
All produce monoclonal light chain immunoglobulin gene rearrangements, or both
Mature B cell lymphomas
39
Derived from circulating IgM, IgD B-cells
Small Lymphocytic Lymphoma/CLL
40
positive for CD19, CD20, and CD23 (+/- CD5)
Small Lymphocytic Lymphoma/CLL
41
Linked to t(11;14) defect
Mantle Cell Lymphoma
42
CD5, CD19, CD20; but negative for CD23!
Mantle Cell Lymphoma
43
Linked to t(14:18) and (q32;q21) - positive for CD19 and CD20
Follicular Lymphoma
44
- Diffuse proliferation of large lymphocytes (Twice the size of normal lymphs) - Most common lymphoma (30-40%)
Diffuse large B cell Lymphoma (DLBCL)
45
- “Starry sky” - CD10, CD19, and CD20 - MYC gene
Burkitt Lymphoma
46
Diagnosis is considered a medical emergency
Burkitt Lymphoma
47
skin presentation stage of a T cell lymphoma
Mycosis Fungoides
48
Typically see pruritus, followed by weepy erythroderma
Mycosis Fungoides
49
Mycosis fungoides is THE most ____ cutaneous lymphoma
common
50
P.B presentation stage of T cell lymphoma
Sezary syndrome
51
Sezary syndrome has _____ prognosis
BAD
52
"butt cells"
Sezary Syndrome (not specific for this)
53
Topical chemo. & superficial radiation for _____ _______
mycosis fungoides
54
HAART
Highly Active Antiretroviral Therapy
55
increases CD4 counts, unfortunately does not ↓ rate of incidence of HIV-related lymphomas
HAART
56
- HIV infection increases general lymphoma risk (by ~ 60X) - Many types (NHL, HL, Burkitt’s, etc.) may occur, especially late in AIDS - Usually very aggressive
HIV-Related Lymphoma
57
MM occurs when a tumor of ________ overgrows in the bone marrow
malignant plasma cells
58
plasma cells that contain ____ ______(rounded accumulations of IG in rER), are called Mott cells/grape cells/morula cells
Russell bodies
59
Plasma cell seen in IgA myeloma is called a ___ ___
flame cells
60
_______(starch-like protein deposits) are deposited throughout body, causing multiple organ defects
Amyloid
61
_____ – new drug; strengthens bones
Aredia
62
Occurs when absolute # of circulating plasma cells exceeds cutoff (>2000/uL)
Plasma Cell Leukemia (PCL)
63
proteasome inhibition causes more _______ in malignant cells than in normal cells!
apoptosis
64
Malignant plasmacytoid lymphocytes
Waldenstrom's Macroglobulinemia (WM)
65
- Oversecretion of IgM - Abnormally increased CD20 cell surface markers
Waldenstrom's macroglobulinemia
66
moderate rouleaux in p.b.
Multiple Myeloma
67
Length of survival - WORSE
Multiple myeloma
68
More common prevalence
Multiple Myeloma
69
Rare hepatosplenomegaly
Multiple Myeloma
70
Marked lytic bone lesions
Multiple Myeloma
71
May occur as end-stage sequela of MM or by itself
Plasma Cell Leukemia