Lymphoreticular pathology Flashcards

1
Q

What makes up the primary immune system?

A

bone marrow, thymus

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2
Q

What makes up the secondary immune system?

A

lymph nodes, spleen, MALT

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3
Q

What cells are inside the bone marrow?

A

Haemopoietic stem cells

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4
Q

What can haemopoietic stem cells become?

A

MYLOID PROGENITOR CELLS - platelets, eosinophils, basophils, neutrophils, monocytes, erythrocytes
LYMPHOID PROGENITOR CELLS - T cells, B cells

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5
Q

What makes up a lymph node?

A

Afferent lymph vessel
Primary lymphoid follicle ( B cell area)
Secondary lymphoid follicle
Germinal centre
Medullary cords (macrophages and plasma cell area)
Efferent vessel

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6
Q

How do we classify lymphoreticular disorders? (cancers)

A

Benign - reactive lymph node

Malignant - lymphocytic leukaemia, lymphomas, myeloma

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7
Q

What predisposes (causes) someone to lymphoreticular disorders?

A

Infective - acute (bacterial, viral), chronic (TB)
Autoimmune
Immunocompromised
Unknown

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8
Q

What is leukaemia?

A

Malignant clonal proliferation of one of the bone marrow cell lines - white blood cells
Acute (ALL, AML) or chronic (CLL,CML)

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9
Q

What causes leukaemia?

A

Multifactorial
Host factors
Random
Damage to DNA during cell division

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10
Q

Describe ALL?

A
Acute lymphoblastic leukaemia
Overproduction and accumulation of cancerous, immature white blood cells (lymphoblasts)
Most common childhood
Cure 60- 90%
Age 2 - 10 yrs
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11
Q

Describe AML?

A

Acute myloid leukaemia
Possible involvement of all cell lines
Overproduction of immature white blood cells, called myeloblasts or leukaemic blasts. These cells crowd the bone marrow, preventing it from making normal blood cells.

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12
Q

What are some oral signs of leukaemia?

A
lymphadenopathy
nerve palsy
infection
hyperplasia
bleeding
hairy leukoplakia
ANUG
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13
Q

What problems may occur secondary to treatment?

A
Bone marrow failure due to irradiation
Salivary gland damage
Swelling 
Dry mouth
Osteonecrosis
Mucositis
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14
Q

Describe CML?

A

Chronic myloid leukaemia
Production of pleuripotent stem cells together with philadelphia chromosome (9 and 22 translocation)
Non specific symptoms - malaise, weight loss
Mainly adults

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15
Q

Describe CLL?

A

Chronic lymphocytic leukaemia
Clonal proliferation of mature B cells
Painless, lymphadenopathy, recurrent infections, anaemia
Elderly

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16
Q

What is a lymphoma?

A

Malignant proliferation in lymph nodes

Two forms : Hodgkins and Non - Hodgkins

17
Q

What is the difference between leukaemia and lymphoma?

A

LEUKAEMIA - proliferation of WBC - circulating cells

LYMPHOMA - proliferation of cells originally in one place - static tumour

18
Q

What is Hodgkins lymphoma?

A

Malignant proliferation of atypical lymphocytes with a reactive inflammatory background within a lymph node
M>F 20-30 yrs and then 50-60 yrs
Many types : nodular sclerosing, mixed cellularity, lymphocyte depletion, lymphocyte rich
Linked to EBV and HIV
Present with reed - sternberg cells which are multinucleatd enlarged leukocytes
Symptoms - lymphadenopathy, splenomegaly, sweats, fever, weight loss

19
Q

What is Non - Hodgkins lymphoma?

A

Slow growing, incurable and non aggressive or fast growing, aggressive, cureable, sudden
Most common in B cell
Destruction of normal nodal architecture, capsular invasion, and extension to soft tissues
Can arise outside the lymph node
Symptoms - lymphadenopathy, lesions intra-orally,
Lined to Sjogrens syndrome

20
Q

How does lymphadenopathy present?

A

Local or generalised

21
Q

What is the cause of local lymphadenopathy?

A

Infection, inflammation

22
Q

What is the cause of generalised lymphadenopathy?

A

Lymphoma, RA, HIV

23
Q

What is the prognosis for leukaemia?

A

Depends on the grade, type and stage
Stage 1 - involves single lymph node or localised organ
Stage 2 - 2+ lymph nodes on same side of diaphragm
Stage 3 - lymph nodes on both sides of diaphragm
Stage 4 - organs with or without lymph nodes, distal involvement

24
Q

What is the treatment for leukaemia?

A

Radiotherapy

Chemotherpay

25
Q

What is a multiple myeloma?

A

Proliferation of lymphoid cells where the malignant cells show differentiation towards plasma cells.
Common in the elderly
Plasma cells produce Ig’s
Presents as jaw lesions, soft tissue mass, bone pain, tenderness, anaemia, impaired renal function

26
Q

How do we treat multiple myeloma?

A

Chemo