Non-hodgkins lymphoma Flashcards

(39 cards)

1
Q

Differences between HL and NHL

AGE

A

Bimodal 15-30 and 50 yrs in H

Increaseswith age, median age being 50. Low grade NHL is 55-60

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2
Q

Gender difference

A

M;F =5;1 IN H

M;F=7;1 IN NHL

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3
Q

Hodgkins lymphoma

A

More in males

rises in adolescence peaks in 3rd decade

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4
Q

Stages difference

A

stages 1 and 2 at presentation in H

stages 3 and 4 at presentation in NHL

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5
Q

b symptons and signs

A

25-40% in H

15% in NHL

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6
Q

direction of spread difference

A

predictable axial spread in H

Random spread in NHL

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7
Q

Leukemic phase

A

rare in H

Common in NHL

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8
Q

ORIGIN DIFFERENCE

A

MAjority originate from nodal region -H

80% nodal and 20% extranodal NHL

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9
Q

Trochlear, mesenteric, pharyngeal nodes

A

Rarely involves these areas-H

Occasional involvement-NHL

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10
Q

mediastinum involvement

A

50% involvement-H

20% NHL

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11
Q

Lymph node involvement

A

subdiaphragmatic LN. gENERALISED ln AND EXTRA LYMPHATIC DX LATER-H

Widespread LN involvemenr- NHL

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12
Q

Bone marrow involvement

A

less than 10% in H

70% in NHL

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13
Q

Spread

A

Contiguous-H

Non contiguous- NHL

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14
Q

GIT AND LIVER INVOLVEMENT

A

Rare-H

COMMON-NHL

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15
Q

Superior vena cava obstruction

A

Common-NHL

Non common- H

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16
Q

CAUSES OF NHL

A

EBV
HTLV 1
immunosuppression

17
Q

First implicated virus

18
Q

What type of infection by EBV is associated with lymphomas

19
Q

Type 1 EBV latency causes

A

burkitts lymphoma

20
Q

Type 2 EBV latency causes

A

hodgkins dx

nasopharyngeal ca

21
Q

Type 3 EBV latency causes

22
Q

Classification of NHL

A

Indolent NHL
B cell lymphomas
T cell lymphomas

23
Q

Examples of B cell lymphomas

A
Diffuse large B cell lymphomas
Follicular lymphoma
Mantle cell lymphoma
Marginal zone lymphomma
Burkitts lymphoma
Lymphoplasmacytic lymphoma
24
Q

Example of T cell lymphoma

A

Cutaneous T cell lymphoma
Angioimmunoblastic T cell lymphoma
Anaplastic large cell lymphoma
Enteropathy type t cell lymphoma

25
Investigations in NHL
Investigation of waldeyers group of LN Bone biopsy
26
is staging laparatomy justifies in NHL
no
27
Symptom status B meaning
unexplained fever Drenching night weats weight loss greater than 10%
28
Bulk
Mediastinal mass greater than 1/10 the max diameter of the chest
29
Recommendations for clinical imaging
``` size - >1.5 Spleen- physical exam,Chest X rat, CT Lymph angiography to identify abnormal LN Gallium scan MRI ```
30
Clinical features of NHL
Lymphadenopathy-widespread Hepatosplenomegaly Fever, night sweats, weight loss
31
Systemic symptoms and signs
due to involvement of particular organs like GIT, lungs, CNS Can cause delay in diagnosis and can decrease survival
32
Less frequent symptoms
``` abdominal pain fatigue painful adenopathy malaise dysphagia cough bone pain edema pruritus ```
33
Burkitts lymphoma presents with
extranodal dx in the jaw in africa in GIT and intraabdominal sites in the west
34
Lymphoblastic lymphoma symptoms
Thymic mass Systemic symptoms Bone marrow failure
35
In advanced NHL about half obtain
Complete remission | the rest obtain useful dx control
36
Those who have complete remission
Relapse in 5 yrs
37
Front line therapy being studied
Fludarabine and 2 chloro deoxyadenosine
38
Management of treatment failures
Repeat previous combination after a long period of remission Quick relapse after chlorambucil; give CHOP/fludarabine
39
Valuable in 2/3 of patients heavily pretreated
Fludarabine, mitoxantrone, dexamethasone