Chronic Inflammation Flashcards

1
Q

Define chronic inflammation

A

Chronic inflammation is chronic response to injury with associated fibrosis

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2
Q

State the cells primarily found in chronic inflammation

A

Macrophages, lymphocytes, plasma cells, eosinophils, fibroblasts/myofibroblasts

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3
Q

Describe the role of macrophages in chronic inflammation

A

Derived from blood monocytes
Various levels of activation
Functions - phagocytosis
Presentation of antigen to immune system
Synthesis of cytokines, complement components, blood clotting factors, proteases
Control of other cells by cytokine release

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4
Q

Describe the appearance and role of lymphocytes in chronic inflammation

A

Small blue dots - large nucleus and small cytoplasm
Mainly immunological function
B lymphocytes differentiate to produce antibodies
T lymphocytes involved in control and some cytotoxic functions

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5
Q

Describe the appearance and role of plasma cells in chronic inflammation

A

Open nucleus (clot face), lumps of chromatin around nucleus
Can see cytoplasm and Golgi (pale area)
Differentiated antibody-producing B lymphocytes

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6
Q

Describe the appearance and role of eosinophils in chronic inflammation

A

Stains bright pink
Bi-lobe nucleus
Allergic reactions, parasite infestations, some tumours

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7
Q

Describe the role of fibroblasts in chronic inflammation

A

Recruited by macrophages, make collagen - cause scarring

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8
Q

Describe the different types of giant cells and where they are classically seen

A

Langhan’s type giant cells - horseshoe of nuclei around periphery
Associated with tuberculosis
Foreign body type giant cells - disorganised irregular aggregated nucleus with foreign material in the middle
Cement and metal in replacement, sand in injury, stitches, fracture where bone moves to new place
Touton giant cell - fat necrosis (high lipid content)

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9
Q

What are giant cells

A

Giant cells - frustrated phagocytosis - macrophages can’t phagocytose
Multinucleate cells made by fusion of macrophages

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10
Q

Describe the situations where chronic inflammation arises

A

Acute inflammation that does not get better
If acute inflammation damage is too severe to be resolved within a few days
De novo - autoimmune conditions, chronic infections (viral hepatitis), ‘chronic low level irritation’
Develop alongside acute inflammation in severe, persistent or repeated irritation
Prolonged exposure to toxic agents

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11
Q

Describe the possible complications of chronic inflammation

A

Abnormal fibrosis - replace normal tissue and impair function of liver
Eg. Gall bladder (chronic cholecystitis), chronic peptic ulcers, cirrhosis
Impaired function - immune system attacks own cells
Eg. Chronic inflammatory bowel disease
Rarely increased function - eg. Mucus secretion, thyrotoxicosis
Atrophy - eg. Gastric mucosa, adrenal glands
Stimulation of immune response - eg. Macrophages - lymphocyte interactions

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12
Q

Chronic cholecystisis description

A

Abnormal fibrosis
Gall bladder with thickened fibrotic wall
Yellow pigment stones
Repeated attacks of acute inflammation
Repeated obstruction by gall stones - tries to move obstruction leading to inflammation

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13
Q

Define granulomas

A

Groups of epitheloid macrophages and lymphocytes that stick together
Histiocytes = macrophages
Epitheloid - looks like epithelium where cells stuck together

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14
Q

Describe the causes of granulomas

A

Irritant foreign material (cement and metal in replacement, sand in injury, stitches, fracture where bone moves to new place)
Infections
Idiopathic granuloma diseases (unknown causes)
Sarcoid, Wegener’s granulomatosis, Crohn’s disease

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15
Q

Rheumatoid arthritis presentation, microscopic features, rheumatoid nodule description

A

Presentation - swelling, stiffness
Microscopic - finger like projections of inflamed epithelial cells, macrophages, lymphocytes, plasma cells
Nodules - swelling with inflammatory cells and necrosis inside

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16
Q

Ulcerative colitis presentation, differential diagnosis, microscopic and macroscopic appearance, complications

A

Presentation - bloody diarrhea, abdominal pain, constipation
Differential diagnosis - Crohns, GI infection
Microscopic/Macroscopic - crypt abscess, distorted crypt architecture, inflammation superficial (mucosa and submucosa)
Complications - severe bleeding, increased risk of colon cancer, liver disease, joint pain, skin ulcers

17
Q

Crohn’s disease presentation, differential diagnosis, microscopic and macroscopic appearance, complications

A

Presentation - abdominal pain, diarrhea
Microscopic/macroscopic - ‘cobblestone’ appearance to bowel mucosa, granuloma present, anal lesions, bowel fistulae
Complications - obstruction and perforation of small intestine, risk of colon cancer, skin ulcers, liver disease, joint pain

18
Q

Distinguish between Crohn’s disease and ulcerative colitis

A

Ulcerative colitis limited to colon, Crohn’s affects any part of GI system
Ulcerative colitis limited to mucosa and submucosa, Crohn’s transmural (entire wall) inflammation
Crohn’s has ‘cobblestone’ appearance, discontinuous distribution, granulomas present, anal lesions, bowel fistulae
Ulcerative colitis has distorted crypts, crypt abscesses

19
Q

Helicobacter pylori associated chronic gastritis role of bacteria, microscopic appearance, complications

A

Bacteria stimulates production of pro-inflammatory cytokines and by directly injuring epithelial cells and increasing acid secretion
Microscopic - chronic inflammation in epithelial and lamina propria layer, lamina propria fibrosis, mucosal atrophy, intestinal metaplasia
Complications - gastric adenocarcinoma, MALT (mucosal associated lymphoid tissue) lymphoma

20
Q

Cirrhosis description, microscopic and macroscopic appearance, causes, complications

A

Fibrosis (scarring) and impaired function of liver
Microscopic - regenerative nodules of hepatocytes surrounded by fibrous tissue that bridges between portal tracts, lymphocytes
Bands of fibrosis tissue
Causes include alcohol, obesity, hepatitis, drugs, toxins, fatty liver disease
Complications - portal hypertension, oedema in legs, splenomegaly, bleeding, infections, malnutrition, jaundice

21
Q

Tuberculosis pathophysiology, microscopic appearance, differentiation from sarcoidosis

A

Mycobacterium tuberculosis bacteria (MTB) enters macrophages by endocytosis, replicates within phagosome and proliferates
After 3 weeks, T-helper cells response which activates macrophages
Activated macrophages produce TNF, recruits monocytes which differentiate into granulomas
Results in tissue damage and infection
Microscopic - langhans giant cells, caseous necrosis
Differentiation - sarcoidosis have discrete separate granulomas, no caseous necrosis, microRNA produced in inflammatory response detected in blood test

22
Q

Sarcoidosis presentation, microscopic appearance

A

Presentation - fever, fatigue, airflow obstruction in lungs

Microscopic - granuloma with no caseous necrosis