Lymphoma Flashcards

(32 cards)

1
Q

Histological Features of Hodgkin Lymphoma (HL)

A

Reed-Sternberg cells (RS cells)

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

HL positive for ……… , but often negative for standard B-cell markers (CD19, CD20, CD21, CD22).

A

CD15+ and CD30+

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

Clinical Features of HL :
Most commonly presents as lymphadenopathy :

A

o Neck (cervical, supraclavicular nodes) most common.
o Non-tender, firm, rubbery nodes.
o May present as an anterior mediastinal mass.

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

Predictable spread for HL

A

from one lymph node group to the next.

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

Key diagnostic test: for HL

A

Lymph node biopsy.
o Presence of Reed-Sternberg cells confirms HL.

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

Risk factors for HL

A

o Epstein-Barr virus (EBV) infection.
o Immunosuppression (HIV, transplant).
o Autoimmune diseases (RA, SLE).

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

WHO Classification of HL

A

Classical Hodgkin Lymphoma (cHL)
Nodular Lymphocyte-Predominant HL (NLPHL) (rare).

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

Classical Hodgkin Lymphoma (cHL)

A

o Nodular Sclerosing HL (most common, 60-80%).
o Mixed Cellularity HL (inflammatory infiltrate).
o Lymphocyte-Rich HL (excellent prognosis).
o Lymphocyte-Depleted HL (poor prognosis).

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

Staging via PET/CT scan (Lugano classification) for HL

A
  1. Stage I: Single node or group.
  2. Stage II: Multiple nodes on one side of the diaphragm.
  3. Stage III: Nodes on both sides of the diaphragm.
  4. Stage IV: Extranodal disease (e.g., liver, bone marrow).
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Treatment:of HL

A

o Chemotherapy + radiation.
o Common regimen (ABVD):
 Adriamycin (Doxorubicin).
 Bleomycin.
 Vinblastine.
 Dacarbazine

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

Classification of NHL

A
  1. Based on Cell Type:
    o B-cell NHL (most common).
    o T-cell NHL.
  2. Based on Growth Pattern:
    o Aggressive (rapid growth, B symptoms).
    o Indolent (slow-growing, waxing/waning course).
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Most common NHL.

A

Diffuse Large B-Cell Lymphoma (DLBCL

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

CD19+, CD20+

A

Diffuse Large B-Cell Lymphoma

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

Diffuse Large B-Cell Lymphoma treatment

A

rituximab (anti-CD20 antibody).

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

t(14;18) translocation → BCL2 overexpression.

A

Follicular Lymphoma:

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

Can transform into DLBCL (poor prognosis)

A

Follicular Lymphoma

17
Q

t(11;14) translocation → Cyclin D1 overexpression.

A

Mantle Cell Lymphoma:

18
Q

Poor prognosis (median survival: 3-4 years).

A

Mantle Cell Lymphoma

19
Q

Associated with chronic inflammation

A

Marginal Zone Lymphoma (MZL)

20
Q

Marginal Zone Lymphoma (MZL)
o Associated with chronic inflammation
Include

A

 MALToma (H. pylori infection → stomach lymphoma).
 Sjogren’s syndrome (salivary gland lymphoma).
 Hashimoto’s thyroiditis (thyroid lymphoma).

21
Q

Highly aggressive B-cell malignancy.

A

Burkitt Lymphoma

22
Q

t(8;14) translocation → c-myc activation

A

Burkitt Lymphoma

23
Q

“Starry sky” histology.

A

Burkitt Lymphoma

24
Q

Strongly linked to Epstein-Barr virus (EBV).

A

Burkitt Lymphoma:

25
There are 3 forms of Burkitt Lymphoma
 Endemic (African): Facial/mandibular mass.  Sporadic: Abdominal involvement.  Immunodeficiency-associated (HIV).
26
B cell NHL
Diffuse Large B-Cell Lymphoma (DLBCL) Follicular Lymphoma Mantle Cell Lymphoma Marginal Zone Lymphoma (MZL) Burkitt Lymphoma
27
T-Cell NHLs
Adult T-Cell Leukemia/Lymphoma (ATLL) Cutaneous T-Cell Lymphomas (CTCL)
28
Presents with lymphocytosis, skin lesions, and lytic bone lesions with hypercalcemia
Adult T-Cell Leukemia/Lymphoma (ATLL)
29
Caused by HTLV-1 virus
Adult T-Cell Leukemia/Lymphoma (ATLL)
30
Adult T-Cell Leukemia/Lymphoma (ATLL) is ………… prognosis.
Poor prognosis (rapidly fatal in months)
31
Sezary syndrome
 Diffuse skin involvement (erythroderma).  Circulating Sezary cells (malignant T-cells with "cerebriform" nuclei).
32
Diagnosis of lymphoma relies on
biopsy, immunophenotyping, and genetic studies.