Week 9 Flashcards

1
Q

What is immunohistochemistry used for

A

Diagnostic use
Metastatic cancer
Looking at response to treatment

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2
Q

Describe epithelium - Arrangement, types, forms what surfaces? What sits below this layer?

A

Closely packed
Form membranes or glands
Separated from connective tissue by basement membrane
Squamous, columnar, cuboidal cells

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3
Q

Describe layers and purpose of stratified epithelium

A

Two or more cell layers

Purpose = protection

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4
Q

Describe the layers and purpose of transitional epithelium

A

Type of stratified - Transitional epithelium is a layer of cells that forms the mucosal lining of your ureters, a portion of your urethra, and your urinary bladder. These cells are called transitional because they can undergo a change in their shape and structure.

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5
Q

What is connective tissue composed of? And purpose

A

Extracellular matrix - Fibres, amorphous ground substance, ECF
A few cells - fibroblasts, adipocytes, macrophages, lymphoid cells (plasma, leucocytes)
Purpose = structure and metabolic support

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6
Q

What do adipose cells look like under a light microscope?

A

Look like clear gaps - because the dye shows where the fat cells were

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7
Q

What is cartilage? What are the different types?

A

Supporting framework

Hyaline cartilage (articular bone)
Elastic (ear)
Fibrocartilage (intervertebral discs)
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8
Q

Purpose of bone (3)

A

Support
Protect
Hemopoiesis

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9
Q

What are the three types of muscle? Describe

A

Skeletal - Striated, attached to skeleton
Smooth - No striations, present in hollow organs
Cardiac - connected by intercalated discs with gap junctions

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10
Q

Define metaplasia, dysplasia, neoplasia

A

Metaplasia - One cell type switched for another (ex. Squamous now columnar)
Dysplasia - Abnormality of development
Neoplasia - Abnormal and excessive growth of tissue (can be benign or malignant)

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11
Q

Describe the basic structure of GI tract from lumen outwards (5)

A

Mucosa (epithelium, lamina propia, muscularis mucosae), submucosa, muscularis propia, subserosa, serosa/adventitia

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12
Q

Three parts of the mucosa

A

epithelium, lamina propia, muscularis mucosae

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13
Q

Which structures have adventiatia rather than serosa?

A

Eosphagus and lower rectum (structures outside peritoneal cavity)

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14
Q

What lines the lumen of the oesophagus?

A

squamous epithelium

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15
Q

Causes of GORD

A

Pregnancy/obesity, hiatal diaphragm, stress, smoking, drinking

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16
Q

What are the key cells involved in inflammation during GORD

A

neutrophil polymorths

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17
Q

Complications of GORD

A

peptic ulceration, replacement of squamous mucosa by glandular mucosa
Stricture
Cancer risk increases

18
Q

What is granulation tissue?

A

Found during repair - loose arrangement of fibroblasts with new capillaries coming to repair

19
Q

What is barrett’s oesphagus?

A

Squamous mucosa undergoes metaplasia from normal squamous epithelium to columnar / glandular mucosa
Two types
Gastric - no goblet cells
Intestinal metaplasia - goblet cells

20
Q

How do you characterise dysplasia? (3)

A

Premalignant change

Impaired cell differentiation
Atypical nuclear features
Increased mitsosi

21
Q

adeno

A

glandular cell origin

22
Q

Two types of adenocarcinoma of oesophagus

A

Intestinal types

Diffuse (signet-ring cell) type

23
Q

Where do squamous cell vs adenocarcinoma tend to occur (most commonly)?

A

SCC - mid/upper oesophagus

AC - Lower oesophagues, gastro-oesophageal junction

24
Q

Cell types involved in gastritis

A

Plasma cell, lymphocyte, neutrophil

25
Main causes of inflammation in the gut (2)
NSAIDs | H. pylori
26
What are the complications of stomach/duodenum ulcers? (5)
Iron deficiency anaemia Erosion of a major submucosal blood vessel (haematemesis, melaena) Perforation into peritoneal cavity (chemical peritonitis) Erosion into an adjacent organ (like pancreas) Healing with scar formation, narrowing
27
Various sensations from within the gut - discuss examples (from top to bottom) (8)
``` Oesophageal distension Gastric distension (fullness) Nutrient density in stomach/duodenum Nausea (toxins or excess nutrients) Movement of gas Pain Urgency Awareness of rectal content ```
28
What are the mechanisms behind visceral sensation?
Afferent nerves send signals to CNS
29
Types of sensory neurons in the gut? (6)
``` Intraganglionic afferent Enteric viscerofugal neuron Intramuscular Vascular afferent Muscular-mucosal Mucosal afferent ```
30
Role of mucosal afferents
Respond to mucosal distortion / stroking
31
Types of pain (4)
Somatic - musculoskeletal, cutaneous, well localized | Visceral - hollow organs, smooth muscle, usually referred (poorly localized)
32
Which organs are not sensitive to pain? Why?
Liver, lungs, kidneys, others | No nociceptors
33
Examples of stimuli for visceral pain (6)
``` Hollow organ distension Traction Ischaemia Acid/irritant chemicals Inflammation Electrical stimulation 'pinching' does NOT cause pain ```
34
Describe pain caused by structural vs functional causes
Structural - inflammatory, neoplastic | Functional - IBS (inclu bloating), dyspepsia (inclu. nausea)
35
Visceral pain becoming somatic - describe example
Acute appendicitis xxx
36
Describes levels of hypersensitivity to pain (3)
Hyperalgesia (primary, local) Allodynia (to non-painful stimuli) Secondary hyperalgesia (generalised)
37
When is it best for patients to take PPI?
30 mins before meal
38
Signs that may differentiate gastric from duodenal pain
Duodenal - often awakens patient at night, 2-3 hrs after meal, relief from meal Gastric - less relief from food/antacids, symptoms shortly after meal
39
tachyphalyxis
lack of response to treatment develops over time
40
Treatment options for GORD (3 types, with examples)
Lifestyle Medical - antacids, alginates, H2RA, PPI, prokinetics Surgical - fundoplication