Hodgkins Lymphoma Flashcards

1
Q

generally occurs at multiple nodal sites and its spread to other lymphoid or extranodal sites is random

A

non‐Hodgkin Lymphoma (NHL)

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2
Q

stage: constitutional symptoms of fever, night sweats, weight loss

A

B

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3
Q

CD15 and CD30 negative

A

Lymphocyte predominant

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4
Q

usually no fevers night sweats

A

stage I or II

Nodular sclerosis and lymphocyte predominant

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5
Q

generally will arise in a single lymph node chain and will spread to adjacent sites in a contiguous pattern

A

Hodgkin Lymphoma (HL)

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6
Q

The lacunar cells express (1)

A

CD15, CD30 and PAX5 a pan B‐cell marker; nodular sclerosis

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7
Q

a variant of the Reed‐Sternberg cell which shows a large clear space surrounding the nucleus

A

lacunar cell; refers to nodular sclerosis

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8
Q

CD15, CD30 and PAX5 a pan B‐cell marker

A

lacunar cells; nodular sclerosis

also seen in mixed cellularity, lymphocyte rich and lymphocyte depletion

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9
Q

constitutional B symptoms - weight loss, night sweats, fever

A

Mixed cellularity and lymphocyte depletion stage III or IV

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10
Q

promotes survival and proliferation of lymphocytes along with survival of germinal B‐cells that would normally be destined to undergo apoptosis but instead produce Reed‐Sternberg cells

A

NF‐Κb activation

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11
Q

stage: one side of diaphragm

A

stage II

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12
Q

shows characteristic nodules surrounded by bands of collagenous tissue and containing mixtures of lymphoid cells, inflammatory cells and lacunar cells

A

nodular sclerosis

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13
Q

It is interesting to note that (1) in (2) have striking resemblance to Reed‐Sternberg cells again suggesting the role of (3) in the pathogenesis of HL

A
  1. EBV infected B‐cells 2. infectious mononucleosis 3. EBV
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14
Q

older patients and in HIV+ patients of any age

A

Lymphocyte depleted

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15
Q

(1) has also been shown to be effective in treatment with much less toxicity

A
  1. Anti CD30
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16
Q

only rarely shows Reed‐Sternberg cells

A

lymphocyte predominant

17
Q

typical B‐cell markers CD20 and BCL6

A

Lymphocyte predominant

18
Q

(1) is a significant part of the pathogenesis in HL. It is believed to occur from (2)

A
  1. NF‐Κb activation( a transcription factor) 2. EBV infection
19
Q

Reed‐Stern berg cells are easily found and they are set in a rich inflammatory background of lymphocytes, plasma cells and numerous eosinophils

A

mixed cellularity

20
Q

Fever, night sweats, constitutional B symptoms

A

mixed cellularity

21
Q

How to diagnosis HL

A

Physical exam for lymph nodes

CT scan to stage disease

bone marrow biospy

22
Q

Liver, spleen and bone marrow involvement may also occur

A

nodular sclerosis

23
Q

features a multilobed nucleus resembling a popcorn kernel and is called a “popcorn cell”

A

lymphocyte predominant

24
Q

stage: single lymph node region

25
stage: disseminated
IV
26
stage: both sides of diaphragm
stage III
27
may transform to DLBCL
Lymphocyte predominant
28
Nodular infiltrate lymphocytes and macrophages
Lymphocyte predominant
29
treatment for low stage disease
radiation therapy
30
stage: asymptomatic
A
31
presents usually as a mass in the cervical, supraclavicular or commonly the mediastinal area in young adolescents
Nodular Sclerosis type HL
32
Stereotypic spread of HL
nodal --\> splenic --\> bone marrow
33
can develop second malignancies of lung, breast cancer or even melanoma
radiation therapy for low stage disease
34
germinal center or post germinal center BCells in origin
Reed‐Sternberg cell
35
second malignancies such as Acute Myeloid Leukemia
chemotherapy for advanced Stage III or Stage IV disease
36
Reed‐Sternberg cell
Hodgkin Lymphoma (HL) cell with owl eye nucleus
37
Most of the tumor will consist of mixtures of inflammatory cells such as (1) in Hodgkin Lymphoma (HL)
1. lymphocytes, plasma cells and frequently numerous eosinophils