Lymphoma - Non-Hodgkin Flashcards

1
Q

How does lymphoma differ from leukaemia

A

The neoplastic cells predominantly involved the lymph nodes and extra nodal sites, unlike leukaemia which mainly involves the bone marrow + blood

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2
Q

Epidemiology

A

50+
MALE

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3
Q

Risk Factors

A

Infection: HIV, EBV, H.pylori
Autoimmunity: Hashimotos, Sjorgrens
Immunodeficiency: HIV as well as hereditary immunodeficiency e.g. Wiskott-Aldrich syndrome

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4
Q

Pathophysiology

A

Non-Hodgkin’s Lymphoma can be divided by cell type: proliferation of B cells, T cells, or NK cells or grade: High or Low
- B cell is the most common type (85%)
* Low grade = follicular lymphoma, marginal zone lymphoma, hairy cell leukaemia
* High grade = diffuse large B cell lymphoma (80%)
* High grade = Burkett’s lymphoma (linked to EBV in Africa causes MASSIVE JAW LYMPHADENOMPATHY)
* Mantle cell lymphoma

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5
Q

Signs

A

Lymphadenopathy
- PAINLESS, hard, rubbery, fixed, non-contiguous spread unlike in HL - NOT AFFECTED BY ALCOHOL
Splenomegaly - more common in NHL
Extra nodal disease - bone marrow, thyroid, salivary gland, GI tract, CNS

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6
Q

Symptoms

A

B symptoms:
- Fever, weight loss, night sweats

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7
Q

Investigations

A

FIRST LINE:
- FBC = Low Hb, Platelets, High ESR, lactose dehydrogenase
GOLD STANDARD:
- Lymph node biopsy = will NOT show Reed-Sternberg cells
CT chest, abdo, pelvis
- Ann Arbour Criteria

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8
Q

Treatment

A

R-CHOP
- Rituximab
- Cyclophosphamide
- Hydroxydaunorubicin
- Vincristine (Oncovin)
- Prednisolone
CNS involvement = intrathecal methotrexate
Low grade = radiotherapy may be curative

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9
Q

How does rituximab work?

A

Monoclonal antibodies which binds to CD20 receptors on B cells to cause apoptosis.

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10
Q

Complications

A

Myelosupression + neutropenia sepsis
Tumour lysis syndrome

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