Lymphoma Flashcards

1
Q

define hodgkins lymphoma?

A

lymphomas are disorders caused by malignant proliferations of lymphocytes ->accumulate in lymph nodes causing lymphadenopathy-> can also be found in peripheral blood or infiltrate organs

histologically divided into Hodgkins and non- Hodgkin

s Hodgkin’s lymphoma ( 15% of all lymphomas) diagnosed by presence of reed-sternberg cells (cells with mirror image nuclei)

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2
Q

what is a histopathological feature of Hodgkin’s lymphoma?

A

Reed-sternberg cells ( binucleate lymphocytes)- OWL EYES

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3
Q

what are the signs of Hodgkin’s lymphoma?

A

Painless enlarging mass – enlarged, painless, non-tender, rubbery, superficial

  • Most commonly in the neck
  • Can also be in the axilla or groin

The mass may become painful after alcohol ingestion

Mediastinal lymph node involvement can cause mass effect e.g. bronchial/SVC obstruction

B symptoms of Lymphoma (systemic)

  • Fever > 38 degrees
  • If this is cyclical it is referred to as Pel-Ebstein fever
  • Night sweats
  • Weight loss > 10% body weight in the past 6 months

Other symptoms

  • Pruritis
  • Cough
  • Dyspnoea
  • Chest/abdo pain – if extensive mediastinal adenpathy
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4
Q

what are the B symptoms of a lymphoma?

A

fever > 38 degrees-> if this is cyclical it is referred to as Pel- Ebstein fever Night sweats Weight loss> 10% Of body weight in the past 6 months

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5
Q

what are the 2 divisions of lymphomas?

A

Hodgkins and and non-Hodgkins

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6
Q

Explain the aetiology / risk factors for hodgkins

A

UNKNOWN

Likely to be an environmental trigger in a genetically susceptible individual

EBV genome has been detected in 50% of Hodgkin’s lymphomas

Risk factors

  • FHx
  • EBV
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7
Q

Summarise the epidemiology of Hodgkin’s lymphoma

A

Bimodal age distribution with peak at 20-30 years and more than 50 More common in males (2:1)

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8
Q

What are the appropriate investigations for Hodgkin’s lymphoma?

A

Bloods

Lymph node biopsy

Bone marrow aspirate and trephine biopsy-> Can spread to bone marrow in late stage

Imaging - CXR, CT, PET

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9
Q

What bloods do you need for hodkin’s lymphoma and describe the results?

A

FBC:

  • high WCC
  • Low Hb and plts
  • Leucocytosis
  • High neutrophils
  • High eosinophils
  • High ESR and CRP
  • High LDH (released during cell turnover)

Baseline thyroid, renal and liver functions

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10
Q

What will be seen in the lymph node biopsy in Hodgkin’s lymphoma

A

Reed- sternberg cells

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11
Q

what is the Ann Arbor staging?

A

I= single lymph node region II= 2+ lymph node regions on one side of the diaphragm III= lymph node regions on both sides of the diaphragm IV= extranodal involvment

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12
Q

outline the different letters to describe each stage?

A

A= no systemic symptoms other than pruritis B= presence of B symptoms-> worse prognosis E= extranodal extension S= involvement of spleen

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13
Q

What are the subtypes of Hodgkin’s lymphoma?

A

Mixed cellularity subtype: It is pathologically characterized by a mixture of lymphocytes and Reed Sternberg cells, and is the subtype often noted to have the greatest abundance of Reed Sternberg cells. It has the closest association with Epstein-Barr Virus among all the subtypes.

Nodular Sclerosing subtype: While the nodular sclerosing subtype is the most common type of HL (65-75%), it predominantly occurs in young middle-aged women. Its pathology shows collagen banding separating nodular regions- good prognosis

Nodular lymphocyte predominant subtype: It is pathologically characterized by an abundance of lymphocytes relative to Reed-Sternberg cells. It occurs more often in younger men. This has the best prognosis.

lymphocyte depleted- poor prognosis

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14
Q

define a non-Hodkin’s lymphoma?

A

All lymphomaas without Reed-sternberg cells ( makes 85% of all lymphomas)

most derived from B cell lines-diffuse large B cell lymphoma is commonest

not all centre nodes ( extranodal tissue generarting lymphoma include mucosa- associated lymphoid tissue- eg gastric MALT)

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15
Q

what are the 2 types of non-Hodgkin’s lymphoma?

A
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16
Q

What are the causes of non-Hodkin’s lymphoma?

A

Complex process involving the accumulation of multiple genetic lesions

The changes in the genome in certain lymphoma subtypes have been associated with the introduction of foreign genes via oncogenic viruses (e.g. EBV and Burkitt’s lymphoma)

Radiotherapy

Immunosuppressive agents

Chemotherapy

HIV, HBV, HCV, HTL-V1

EBV and Burkitt’s

H pylori

Connective tissue disease (e.g. SLE)

Sjogren’s

Coeliac’s

17
Q

Outline extranodal disease in non hodgkin’s lymphoma and give the symptoms related to this?

A
extranodal disease ( 50% ) 
**gut ( commonest)**

1) Gastric MALT- caused by H pylori -> symptoms same as gastric cancer
- MALT usually involved altrum, is multifocal and metastasises late
2) non- MALT gastric lymphomas ( 60% ) - usually diffuse large cell lymphomas- high grade and not responding well to H-pylori eradication
3) small- bowel lymphomas eg IPSID) or EATCL- presents with diarrhoea, vomiting, diarrhoea, vomiting, abdominal pain and decreased weigh- poor prognosis

skin ( second most common)

- Eg clonal T cells in mycosis fungoides

Oropharynx

  • Waldeyer’s ring lymphoma causes sore throat, obstructed breathing

other sites- bone, CNS, lung

18
Q

what are the symptoms of non- Hodgkin’s lymphoma?

A

Painless enlarging mass (in neck, axilla or groin) – superficial lymphadenopathy

Systemic Symptoms (occurs less frequently than in Hodgkin’s):

Fever

Fatigue/malaise

Night sweats

Weight loss > 10% body weight

Symptoms of hypercalcaemia

Symptoms related to organ involvement

Extranodal disease is MORE COMMON in NHL than in Hodgkin’s lymphoma

Skin rashes

Headache

Sore throat

SOB – pleural involvement

Cough

Headache/change in mental status – meningeal involvement

Abdominal discomfort

Testicular swelling

Dizziness and ataxia – CNS involvement

Bone and back pain – bone involvement

Jaundice – liver infiltration

19
Q

What are the systemic symptoms of non-Hodgkin’s?

A

less common than in hodkin’s lymphoma and indicates

Fever

Fatigue/malaise

Night sweats

Weight loss > 10% body weight

Symptoms of hypercalcaemia

20
Q

What are the signs of non-Hodkin’s lymphoma?

A

Painless firm rubbery lymphadenopathy

Skin rashes- Mycosis fungoides - pruritic cutaneous plaques - looks like a fungal infection but is in fact a cutaneous T-cell lymphoma

Abdominal mass

Hepatomegaly

signs of bone marrow involvement

  • anaemia
  • infections
  • purpura
21
Q

What are the appropriate investigations for non-Hodkins lymphoma?

A

bloods

blood film- lymphomas may be visible in some patients

bone marrow aspiration and biopsy

imaging- CT, CXR, PET

Lymph Node Biopsy - allows histopathological evaluation, immunophenotyping and cytogenetics

Staging - Ann-Arbor

22
Q

What can be seen in the bloods when investigating a non-Hodkin’s lymphoma?

A

FBC

-anaemia

  • lymphocytosis
  • neutropenia
  • thrombocytopenia

High ESR and CRP

Raised LDH

Renal and liver baseline test s

Calcium may be raised

HIV, HBV and HCV serology

23
Q

summarise Hodkins lymphoma?

A

Hodgkin’s : B cell symp (systemic symp) + lymph N hurts with alcohol + pruritis + NT rubbery lymphadenopathy + reed stern burg cells , associated with EBV - high WCC, low Hb and low plts

24
Q

summarise non-Hodkin’s lymphoma?

A

Non-Hodgkin’s : painless enlarging cervical lymph N + organ involvement (skin rashes, headache, hepatosplenomegaly + sore throat/ cough + BM fail signs) – associated with Sjogrens

Burkitts lymphoma: African, large N in jaw growing quick and starry sky appearance

25
Q

summarise a typical presentation of Burkitt’s lymphoma?

A

subtype of NHL ( B cell)

- African child

- large lymph node in jaw ( fast growing)

- under microscopy- starry appearance