The Lymphoid System Flashcards

1
Q

What are the steps in the production of lymphoid cells?

A

Haematopoietic stem cells - precursor lymphoid cells - maturation in bone marrow or thymus - secondary lymphoid organs

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2
Q

What cells mature in the bone marrow?

A

B cells

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3
Q

What cells mature in the thymus?

A

T cells

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4
Q

What are the central (primary) lymphoid tissues?

A

Bone marrow and thymus

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5
Q

What are the peripheral (secondary) lymphoid tissues?

A

Lymph nodes, spleen, tonsils, epithelio-lymphoid tissues, bone marrow

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6
Q

What are some functions of the lymphatic system?

A

Returns lymph to circulation = important in fluid homeostasis and preventing oedema
Permits cell traffic, cell trapping and interaction of cells and molecules with cells of the immune system

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7
Q

How are lymph node groups identified?

A

Distinct groups can be palpated = cervical, axillary, inguinal
Major groups can be viewed radiologically (e.g para-aortic)

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8
Q

How is lymph drainage by nodes arranged?

A

Groups of nodes drain particular territories

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9
Q

What are lymph nodes?

A

Small oval bodies up to 2cm in size that are located along the course of lymphatic vessels

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10
Q

What are lymphatic vessels?

A

Blind ending vascular channels that collect fluid from tissues and return to bloodstream

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11
Q

What do lymphatic vessels allow?

A

Passive movement of fluid = valves ensure direction of flow

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12
Q

What drains lymph through the capsule of lymph nodes?

A

Afferent channels = drain through capsule and into peripheral sinus

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13
Q

Where does the efferent vessel of the lymph node drain to?

A

Cisterna chyli/thoracic duct
Left jugular, subclavian or bronchomediastinal trunks
Right jugular, subclavian or bronchomediastinal trunks

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14
Q

Where does lymph drain into the venous system?

A

At the junction of the left or right subclavian and jugular veins

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15
Q

Where do the arterial and venous vessels serving the lymph node enter/exit from?

A

At the hilum

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16
Q

Where is lymph filtered in the lymph node?

A

Filtered within the node parenchyma before returning to the bloodstream = traffic of cells between lymph and node parenchyma

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17
Q

How is the lymphoid system involved in the immune response?

A

Houses cells of innate immune system = traffics APCs to link innate and adaptive systems
Seat of adaptive immune response

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18
Q

What lymphocytes are present in the lymphoid system that serve in the immune response?

A

B cells
T cells = T helper cells, T cytotoxic cells
Natural killer cells

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19
Q

What are some features of the B cells involved in the lymphoid system?

A

Associated with follicles and germinal centres = interfollicular, plasma cells (mainly in medulla)

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20
Q

What immune cells does the lymphoid system conatin?

A

Lymphocytes, macrophages, antigen presenting cells (APCs), dendritic cells, endothelial cells

21
Q

What are some CD numbers associated with B and T cells?

A

CD20 is associated with B cells

CD3 is a T cell marker

22
Q

What are some causes of lymphadenopathy?

A

Local inflammation = infection, vaccination
Systemic inflammation = viral infection, autoimmune
Malignancy = metastatic, leukaemia/lymphoma
Others = sarcoidosis, Castleman’s, IgG4 related

23
Q

How should regional lymphadenopathy be examined for?

A

Examine the territory that drains the particular group of nodes

24
Q

What is associated with some causes of superficial inflammation causing regional lymphadenopathy?

A

Lymphangitis = red lines extending from an inflamed lesion, may be first sign of underlying malignancy

25
What is generalised lymphadenopathy a sign of?
A systemic inflammatory process or widespread malignancy = lymphoma/leukaemia are high on differentials (check FBC)
26
What are the different processes that cause lymph nodes to be enlarged?
Predominant B cell response = autoimmune, infection Predominant phagocytic response = draining a tumour site Predominant T cell response = viral infections, drugs
27
Where is the spleen loacted?
High in left upper quadrant of abdomen = usually non-palpable unless substantially enlarged
28
What are the two surfaces of the spleen?
Diaphragmatic and visceral
29
What structures is the visceral surface of the spleen in contact with?
Left kidney, gastric fundus, tail of pancreas, splenic flexure of colon
30
What is the vasculature of the spleen?
Supplied by splenic artery = branch of coeliac axis | Drained by splenic vein = joins with superior mesenteric vein to form portal vein
31
What effect does a disease spleen have on the likelihood of rupture?
Diseased spleen is more likely rupture
32
Is the spleen encapsulated?
Yes
33
What does the parenchyma of the spleen contain?
Red pulp = contains sinusoids and cords | White pulp = contains CD4+ T cells
34
What are some features of splenic sinusoids?
Fenestrated with a lining of endothelial cells | Supported by hoops of reticulin
35
What do splenic cords contain?
Macrophages and some fibroblasts | Cells in transit = RBC, WBC, PC and some CD8+ T cells
36
What are some of the functions of the spleen?
Detects, retains and eliminates unwanted, foreign or damaged red material Facilitates immune response to blood-borne antigens
37
What does the white pulp of the spleen comprise?
Peri-arteriolar lymphoid sheath (PALS) = contains CD4+ T cells and is expanded by lymphoid follicles
38
How does the white pulp of the spleen trigger an immune response?
Antigen reaches white pulp via blood and APCs in the white pulp present antigen to immune reactive cells = T and B cell responses can then occur
39
What are some of the features associated with splenomegaly?
Dragging sensation in LUQ, discomfort with eating, pain (if ischaemia present), hypersplenism
40
What is the triad of hypersplenism?
Splenomegaly, fall in one or more cellular components of blood, correction of cytopenias by splenectomy
41
What are some causes of splenomegaly?
Infection = TB, EBV, malaria, typhoid Congestion and haematological disease Inflammatory conditions = SLE, rheumatoid Storage disease = Gaucher's, Niemann-Pick disease Others = amyloid, tumours, cysts
42
What are some causes of congestion that lead to splenomegaly?
Hepatic cirrhosis, cardiac failure, portal or splenic vein thrombosis
43
What haematological disease cause splenomegaly?
Lymphoma and leukaemia, haemolytic anaemia, ITP, myeloproliferative disorders
44
What is hypersplenism associated with?
Conditions that cause splenomegaly
45
What is the diagnostic test for hypersplenism?
Splenectomy
46
What must be considered in patients with hypersplenism and bone marrow failure?
May have to balance productivity of spleen with its role in excessive removal of circulating blood cells
47
What are the causes of hyposplenism?
Most commonly due to splenectomy | Others = Coeliac, sickle cell disease, sarcoidosis, iatrogenic
48
What is mostly responsible for the features of hyposplenism?
Reduced red pulp function = Howell-Jolly bodies, other red cell abnormalities
49
What can be an additional feature of hyposplenism?
Immune deficiency = especially if spleen is removed in childhood