Lymphoid System Flashcards

1
Q

Where do B cells mature?

A

Bone Marrow

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2
Q

Where do T cells mature?

A

Thymus

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3
Q

What areas are considered Primary Lymphoid Tissue?

A

Central Bone Marrow

Thymus

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4
Q

What areas are considered Secondary Lymphoid Tissue

A
  • Lymph nodes
  • spleen
  • tonsils (Waldeyer’s ring)
  • epithelio-lymphoid tissue (e.g. in bowel/ skin)
  • peripheral bone marrow
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5
Q

What are the functions of the Lymph system?

A
  • return lymph to circulation
  • prevents accumulation of fluid in tissue (oedema)
  • permits cell traffic
  • allows cell trapping (i.e. traps abnormal cells in lymph)
  • cells can interact with immune system
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6
Q

When does lymphoedema commonly appear?

A

post axillary surgery for breast cancer
=> no lymph nodes to drain fluid from arm
=> swelling

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7
Q

What is chylous ascites and when does it occur?

A
  • lipid rich lymph
  • accumulates in peritoneum
  • due to trauma/obstruction
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8
Q

What major lymph node groups must be visualised radiologically?

A

Mediastinal

para-aortic

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9
Q

How large can lymph nodes become when swollen?

A

2.5cm

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10
Q

Describe the passage of lymph through a lymph node

A

IN = afferent lymph vessel
travel round peripheral sinus
diffuse through parenchyma
to EFFERENT lymph vessel

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11
Q

What type of immune cell links the innate and adaptive immune system?

A

Antigen Presenting Cells (APC’s)

present antigen to mature B/T cells in lymph node to create memory bank cells and Ab

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12
Q

B Cells accumulate where in lymph nodes?

A

Germinal Centres

- allows them to differentiate into IgG and memory B cells

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13
Q

Aside from B and T cells, what other cells are found in a lymph node?

A

Natural Killer Cells (NKCs)
Macrophages
APCs
Dendritic Cells

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14
Q

What surface antigens are used to differentiate B and T lymphocytes on immunophenotyping?

A

B cell - CD20

T cell - CD3

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15
Q

What are the potential causes of lymphadenopathy?

A
  • local inflammation (e.g. bacterial infection)
  • systemic inflammation (e.g. viral infection, autoimmune)
  • malignancy (haem or non-haem)
  • metastatic disease

OTHERS: sarcoidosis

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16
Q

What percentage of sarcoidosis cases experience lyphadenopathy

A

15%

17
Q

Sarcoidosis can potentially hide a malignancy in a lymph node. TRUE/FALSE?

A

TRUE

- granulomatous disease can make it difficult to identify other pathology in node

18
Q

How can regional lymphadenopathy be identified on examination?

A
  • red lines may extend from inflamed lesion due to pattern of draining
    => lymphangitis
  • superficial lymphadenopathy (e.g. first sign of underling cancer e.g. breast)
19
Q

A predominant B cell response in a lymph node that is enlarged would make you consider what causes?

A
  • autoimmune

- infection

20
Q

A predominantly phagocytic response in an enlarged lymph node would make you consider what causes?

A

Drainage of a tumour site

21
Q

A T cell response in an enlarged lymph node was cause you to consider what pathology?

A
  • viral infection

- drug induced (phenytoin)

22
Q

GIve an example of a disease during which the spleen is more likely to rupture? How is this prevented?

A
  • glandular fever (EBV)

- encourage patients to not participate in contact sport

23
Q

What types of tissue make up the spleen and what is found in each?

A

Parenchyma includes red pulp and white pulp

Red pulp contains sinusoids and cords which have cells in transit

White pulp contains T helper cellls

24
Q

What is the main function of the spleen?

A

Filters blood like lymph node filters lymph

25
Q

What symptoms do patients experience in splenomegaly?

A
  • dragging feeling
  • pain/discomfort on eating
  • low blood count often seen (due to increased splenic breakdown of blood cells)
26
Q

What can cause splenomegaly?

A
  • infection
  • congestion (portal hypertension)
  • haematological cancer
  • inflammation (RA, SLE)
  • Storage disease (e.g. Goucher’s Niemann-Pick disease)
27
Q

What causes HYPOsplenism?

A
- usually occurs due to splenectomy
OTHERS:
- coeliac
- sickle cell
- sarcoid
- iatrogenic
28
Q

What is usually required in hyposplenism to prevent infection?

A

various vaccinations

prophylactic antibiotics

29
Q

What are Howell Jolly Bodies and what do they indicate

A

DNA nucleated RBCs
- these are usually removed by spleen
=> in HYPOsplenism these are not removed