Chronic Inflamation Flashcards

1
Q

What is chronic inflammation?

A

Chronic response to injury with associated fibrosis

Know less about it at cellular/molecular/signalling level than acute

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2
Q

What are 2 ways call injury leads to tissue repair?

A

Acute insult -> acute inflammation -> if damage is slight resolution is possible
-> if damage is not slight CHRONIC INFLAMMATION - repair and scarring

OR

Chronic insult -> chronic inflammation -> repair and scarring
Ie skipping the acute phase - de novo

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3
Q

How does chronic inflammation arise?

A
  1. May take over from acute inflammation if damage is too severe to be resolved within a few days
  2. May arise de novo
    – Some autoimmune conditions (e.g. RA)
    – Some chronic infections (e.g. viral hepatitis)
    – “chronic low-level irritation”
  3. May develop alongside acute
    inflammation …in severe persistent or repeated irritation
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4
Q

What does chronic inflammation look like?

A

• What does it look like?
– Characterised by the microscopic appearances which are much more variable than acute inflammation.
– Most important characteristic is the type of cell present.

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5
Q

What cells are important in chronic inflammation?

A

Macrophage
• Derived from blood monocytes - monocyte = circulating, macrophage = in tissue (same thing)
• Important in acute and chronic inflammation
• Various levels of activation - not activated until tissue is injured. Long lived whereas polymorphs are short lived

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6
Q

What are the unctions of macrophages?

A

– Phagocytosis and destruction of debris & bacteria
– Processing and presentation of antigen to
immune system
– Synthesis of not only cytokines, but also complement components, blood clotting factors and proteases
– Control of other cells by cytokine release

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7
Q

Describe the appearance of macrophages lymphocytes neutrophils and eosinophils

A

Macrophages - large in comparison to erythrocytes, kidney shaped nucleus off to one side
Lymphocytes - large nucleus, not much cytoplasm
Neutrophils - multi lobed nucleus,
Eosinophils - bilobed nucleus, darker stained colour

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8
Q

Briefly, what are the functions of lymphocytes?

A

Functions:
– Complex, mainly immunological.
– B lymphocytes differentiate to produce antibodies.
– T lymphocytes involved in control & some cytotoxic functions.

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9
Q

Name 3 other cell invoved in the chronic inflammatory response

A

• Plasma cells:
– Differentiated antibody-producing B lymphocytes.
Usually implies considerable chronicity.

• Eosinophils:
– Allergic reactions, parasite infestations, some Timor’s

• Fibroblasts / Myofibroblasts:
– Recruited by macrophages; make collageb

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10
Q

What are giant cells

A
• Multinucleate cells made by fusion of macrophages 
• Frustrated phagocytosis 
• Several types recognised
– Langhans  -> tuberculosis 
– Foreign Body Type 
– Touton -> Fat necrosis
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11
Q

Describe Langhans type giant cell in tuberculosis

A

Pale foamy cytoplasm
Nuclei around the edge
See slide

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12
Q

Describe foreign body type giant cells

A

See slide

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13
Q

Describe Touton giant cells

A
See slide
Cell
Fatty tissue = avascular
Let of fatty material o get rid of 
Clump togteher to make these 
Giant cells
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14
Q

How do cell types vary in different conditions in chronic inflammation

A

• Morphology of most chronic inflammatory reactions is non-specific, BUT proportions of each cell type may vary in different conditions.
• For example:
– Rheumatoid arthritis: Mainly plasma cells.
– Chronic gastritis: Mainly lymphocytes.
– Leishmaniasis (a protozoal infection): Mainly macrophages.
– Giant cell type may be a help to diagnosis.

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15
Q

What are the effects of chronic inflammation?

A
• Fibrosis
e.g. gall bladder (chronic cholecystitis), chronic peptic ulcers, cirrhosis thyrotoxicosis
• Impaired function
e.g. chronic inflammatory bowel disease
– Rarely increased function e.g. mucus secretion, 
• Atrophy (reduction in size)
– gastric mucosa, adrenal glands 
• Stimulation of immune response
– Macrophage - lymphocyte interactions
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16
Q

What is chronic cholecystitis?

A

See slide

  • Repeated obstruction by gall stones
  • Repeated acute inflammation leads to chronic inflammation
  • Fibrosis of gall bladder wall
Mucosal surface normal red here it is whyute
Wall has thickened 10-15x
Repeated attacks of acute inflammation 
Pain 
Removing it is useful

Add more

17
Q

What is inflammatory bowel disease?

A
  • Family of Idiopathic inflammatory disease affecting large and small bowel
  • Patients present with diarrhoea, rectal bleeding and other symptoms
  • Ulcerative colitis and Crohn’s disease

See slide for histology

18
Q

Describe differences between ulcerative colllitis ad chrons disease

A
• Ulcerative colitis is superficial
– Diarrhoea, bleeding
• Crohn’s disease is transmural
– Strictures, fistulae
N.B. Fistula = abnormal connection between two epithelium-lined organs eg loops of bowel come attached to each other
19
Q

What are common causes of cirrhosis?

A
Common causes of cirrhosis 
Alcohol (commonest UK cause)
Infection with HBV, HCV (commonest overall cause)
Immunological 
Fatty liver disease 
Drugs and toxins
20
Q

Describe the appearance and histology of a liver

A
See slide 
Cirrhosis - histological section 
Severe damage leading to cirrhosis
Nodules
Cirrhosis = irreversible
21
Q

What ca lead to cirrhosis?

A

Fibrosis and impaired function

22
Q

What is Graves’ disease

A

Thyrotoxicosis
Antibodies against tosh receptor
GSH normallybinedes to GSH receptor - thyroid hormones produced
Antibodies produced by plasma cells bind to GSH receptor - increased thryroid function
Difficult to manage

23
Q

Describe the histology of gastric musics a atrophy

A
See slide
Reduced function 
Reduction in size of cels 
Atrophied gastritis = autoimmune disease 
Normal gastric mucosa
Tightly packed gastric glands 
Big are where glands gone - replaced by chronic inflammatory cells
Doesn’t produce right acid and enzymes
24
Q

Describe the overlap between inflammation and immune response?

A

• Chronic inflammation and immune responses overlap
– Immune diseases cause pathology by chronic inflammation
– Chronic inflammatory processes can stimulate immune responses

25
Q

What is granulomatous inlammation?

A

Chronic inflammation with granulomas

26
Q

What is a granuloma?

A

Cohesive localised group of chronic inflammatory cells
Macrophages most important (big in the middle)
Histiocyte = old word for monocytes/macrophage
Epitheioid = like epithelium - cells that stick together
Groups of macrophages sticking together like epithelium
Lymphocytes arounfd the Edget helper macrophage communication

27
Q

What causes granulomas?

A
  • Persistent, low-grade antigenic stimulation
  • Hypersensitivity

• Mildly irritant ‘foreign’ material
• Infections
– Mycobacteria: Tuberculosis, leprosy (commonest persistent low grade antigenic stimulation - body struggles to kill these)
– Other infections e.g. some fungi

• Unknown causes
– Sarcoid
– Wegener’s granulomatosis
– Crohn’s disease

28
Q

What are the main causes of granulomatous inflammation?

A

Low grade antigenic stimulation from foreign material
Body struggles to get rid of them
Granulomatous activity to deal with them
Can get this from sutures
Recognise that tehse are the consequences

See slide

29
Q

What is tuberculosis

A

• Caused by Mycobacteria
– especially M. tuberculosis. Difficult & slow
to culture.
• Nature of organism: see microbiologists
– n.b. wall lipids (Mycosides).
• Produces no toxins or lytic enzymes
• Causes disease by persistence and induction of cell-mediated immunity.

Tb can survive in phagolysosomes as it has resistant ell walls
Tb gets into body, survives, illicit inflammatory reaction
Die if Tb proliferates
Can get acute w/pneumonia
Often long term effection = bc of inflammation
Scarrung ->cancer?
Couching
Use=creationsa=carrying in the gut
Reaction to organism - body cant get rid of i t

30
Q

Describe the histology of a tuberculous granuloma in lung

A

See slide

31
Q

What is an indicator for Tb

A

Langhan = indicator that biopsy is Tb
Often show caseous necrosis = cheese like
Pale or pink down microscope

32
Q

Describe BCG granuloma

A

See slide

33
Q

What are some granulomatous diseases of unknown cause?

A

• Sarcoidosis
– Variable clinical manifestations
Young adult women Non-caseating granulomas, giant cells Involves lymph nodes, lungs…
- Sarcoidosis - young ppl - non caseosating granulomatous
Mediastinal lymphadenopathy
Hard to treat
Immunosuppressive but this has consequences
Can ve progressing
Often doesn’t progress
Sarcoidosis in liver can lead to cirrhosis

• Crohn’s Disease
– ‘Regional enteritis’: patchy full-thickness
inflammation throughout bowel
- granulomatous in abt 50%

• Wegener’s granulomatosis
- rarer
- usually affects kidneys
(and many others)

In all - magaement issues = getting diagnosis to see how to treat