Pathalogical Diseases Flashcards

1
Q

What is the link between gallstones and hepatic abscess? What disease can this lead to

A

Blockage is the main problem (blockage of bile duct by gall stones)
Liver produces bile and its important because it emulsifies fat.

It comes down to the hepatic duct and bile duct, the gall bladder joins to as it concentrates the bile and comes from the common bile duct.

Gall stones blocks these ducts and causes bile not to be secreted.

Another purpose is that it releases toxic material to detoxify the body, but if its blocked the body will not be able to detoxify the body.

This will causes infection and causes pus to form. Pus cant pass through so it will go back to the liver which will cause an abscess

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2
Q

Differnce btw osteoarthritis and RA on xray?

A

Loss and less

osteoarthritis

L – loss of joint space
O – osteophytes
S – subchondral sclerosis
S – subchondral cysts

RA

L – loss of joint space
E – erosions
S – soft tissue swelling
S – soft bones (osteopenia)

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3
Q

A 38 year old Afro-Caribbean woman presents with tiredness and a cough. A chest x-ray shows enlarged hilar lymph nodes. What diagnosis can u consider (differentials?)

A
  • TB
  • LYMPHOMA
  • sarcidosis

SHE HAS SARCIDOSIS

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4
Q

explain what happens when Mycobacterium TB enters the lungs

A

once engulfed by the alveoli macrophages, they produce proteins to inhibit lysozomes from englufing them! this allows them to survuce and they also proliferate!>> PRIMARY INFECTION

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5
Q

A 40 year old woman gives a history of joint pain that began in her fingers but then spread to her wrists and ankles. She says her symptoms are worse in the mornings. Metacarpophalangeal and proximal interphalangeal joints of the hands appear most affected. The joints are warm, swollen and painful.

A

Rhematoid arthritis!

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6
Q

what is hereditary angio oedema?

A

autosomal dominaot, inherited deficiency of c1-esterase inhibitor (component of complement system).

  • Episodic attacks of swelling that may affect the face, extremities, genitals, gastrointestinal tract and upper airways.
  • family history of sudden death Disorder of acute inflammation
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7
Q

chronic granulomatous disease

A

deficiency in one of components of NADPH oxidase responsible for generating superoxide.. the bacteria r phagocysted, but cannot be killed, since pahgocytes cannot perform the ‘oxygen burst’ this will result in many chronic infections!

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8
Q

Coal- workers pneumonia (CWP)

what it is

presentation

complications

A

“black lung disease”

is an occupational disease (type of pneumoconiosis) caused by exposure to coal dust free of silica (washed coal).

the spectrum of lung fidings vary from

1) atmpytomic anthracosis

2) simple CWP w/ little or no pulmonary dysfunction

3) complicated CWP w/ fibrosis!

in a nutshell>> prolonged coal dust exposure> alveolar or intersitial macrophages loaded with carbon> Inflammation and FIBROSIS

blackened scars in UPPER LOBE, since its next to the respiratory bronchi (site of initial dust acummalation)

may lead to FIBROSIS> Emphysema & chronic bronchitis

anthracosis: “the asymptomatic, milder type of pneumoconiosis as caused by the accumulation of carbon in the lungs due to repeated exposure to air pollution or inhalation of smoke or coal dust particles”

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9
Q

give complication of gallstones and explain why they occur.

Give four other complications of gallstones and explain why they occur.

A

-jaudndince -bilary cholic -gall stone ileus- -pancretitis

Pancreatitis

Acute cholecystitis

Cholangitis

Obstruction if bile duct

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10
Q

what is TB? describe how the granuloma looks like?

A

-caused by mycobacterium, it doesn’t produce any toxins or lytic enzymes, they just survive, and use the body immune’s reaction to kill the human (causes chronic inflammation) -giant cells r formed, they surround bacteria and cause granuloma, they do this to wall off the bacteria to prevent it from spreading! the tissue in the middle dies as a result causing CASEOUS necrosis.

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11
Q

what type of bacteria can cause a bloody stool?

A

shigella and E coli

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12
Q

what type of giant cell is seen in TB?

A

Langhans giant cell

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13
Q

classification and manifestation and treatment of sarcoidosis

A
  • young adult women (african-american females)
  • non-caseating granulomas, giant cells involves lymph nodes, lung
  • high ACE levels
  • enlarged lymph nodes

Treat: steroids (if symptomatic)

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14
Q

joint findings in osteoarthritis vs rheumatoid arthritis

A

osteoarthritis>> osteophytes, joint space narrowing, synovial fluid noninflammatory, heberdens nodes, does not involve MCP joint

rhematoid: soft tissue swelling, sublimation of fingers, ulnar deviation, swan neck, synovial fluid inflamed, ivolves the MCP joint.

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15
Q

TB symptoms

A

fever, night sweats, cough, weight loss

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16
Q

differentiate btw chron’s disease and ulcerative colitis.

A
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17
Q

what is a paradoxical embolism

A

emboli can pass through an inter-atrial or inter-ventricular defect and gain access to the SYSTEMIC circulation

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18
Q

explain the formation of a granuloma in TB and what is a ghons focus and ghons complex?

when does the granuloma form?

A

3 weeks later after primary infection occured,

the immune system kicks in and immun ecells surround the site of infection making a GRANULOMA. attempting to wall off the bacteria and prevent it from spreading.

the tissue in the middle dies as a result and CASEOUS NECROSIS

this forms a GHONS FOCUS

When Tb goes to near by hilar lymph nodes. there it causes caseation there as well! >> ghon Complex

usually subpleural & seen il lower lobes

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19
Q

what is a Ranke complex in Tb? ghons complex?ghons focus

A

the tissue that is encapsulated by the granuloma undergoes FIBROSIS and CALCIFICATION>> this calcified ghons complex is called a = RANKE COMPELX

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20
Q

What is the definition of an ulcer?

A

Ulcer = breach in mucosa to level of submucosa or deeper.

Breach : make a gap in and break through

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21
Q

How does Helicobacter pylori cause gastritis?

Which malignancies are associated with Helicobacter pylori gastritis? (2)

A

By stimulating production of pro-inflammatory cytokines and by directly injuring epithelial cells and increasing acid secretion.

Gastric adenocarcinoma.

MALT lymphoma.

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22
Q

What r the findings u get in multiple myeloma?

A
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23
Q

Define multiple myeloma?

A

Myeloma is a cancer that affects cells in the bone marrow, called plasma cells. As the cancerous plasma cells fill the bone marrow, you are not able to make enough normal blood cells. This can lead to anaemia, bleeding problems and infections.

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24
Q

Difference btw liver cirhosiss and fibrosis

A

Fibrosis is the first stage of liver scarring. When scar tissue builds up and takes over most of the liver, this is a more serious problem called cirrhosis

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25
Q

a patient with RA, develops subcutaneous lumps on the extensor aspect of her forearms. What are these lumps and how do they appear microscopically?

A

Rheumatoid nodules

is a local swelling or tissue lump, usually rather firm to touch, like an unripe fruit.

Fibrin necrosis in the middle, surrounded by granuloma formation.

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26
Q

how can u distiguish btw Sarcoidoisis and TB?

**hint= blood tests?

A

Xiehl-neelsen stain to stain micro bacterium for suspecting TB. (Mycobacteria dont stain cause they don’t have cell wall. )

ACE>> higher in sarcoidosis

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27
Q

A woman had breast augmentation five years ago. She now presents with distortion and firmness of her right breast. what type of giant cell will be see/n

A

Foreign body giant cell>> nulcei scattered

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28
Q

what is pott’s disease?

A

TB in vertebrae.

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29
Q

what tissues does miliary TB effect?

A
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30
Q

what is Bacillus Calmette-Guérin (BCG)

A

is a vaccine against TB that is prepared

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31
Q

What is a Scrofula?

A

TB nodes in cervical region.

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32
Q

what is an

* Acid fast test

* Mantoux test test

in TB

A

* Acid fast- retains stains even on treatment with mixture of acid and alcohol.

* Mantoux test– a screening test for TB. It is a delayed hypersensitivity

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33
Q

how does Miliary TB form?

A

Ghon focus can be reactivated and spread to the lung.

immune sytem memory T cells releases cytokines to try to control the new outbreak, which forms more areas of caseous necrosis which cavitates>

this allows the bacteria to dissaminate> or spread throughout the lungs> bronchopneumonia

it can also spread via the vascular tissue and effect other tissues in the body!

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34
Q

Ehlers-Danlos syndrome

A
  • inherited disorder
  • procollagen doesn’t convert to tropocollagen
  • Type 3> Three ED
    1) Skin- hyperextensible, thin, fragile & susceptible to injury
    2) Joints – hypermobile, predisposition to joint dislocation

**Because the collagen in internal organs is also affected patients can suffer from rupture of the colon and, in some forms, large arteries. Corneal rupture and retinal detachment can also be seen.

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35
Q

what is scurvy? causes? presentation?

A

vitamen C deficiency > procollagen can’t do hydroxylation in ER > reduced cross- linking and defective helix formation > ppl unable to heal wounds 3adl>tendacy to BLEED

  • bleeding gums
  • loss of tooth

ppl had black bones when they died> bc there was a lot of bleeding in ur bones!

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36
Q

Osteogenesis imperfecta

A

“brittle bone disease” It results in bones that break easily.

TYPE 1 COLLAGEN

Patients have too little bone tissue (osteopenia) and hence extreme skeletal fragility.

  • Blue sclera>due to decreased collagen in the sclera, making it translucent that permits visualisation of the underlying choroid
  • Hearing loss> due to abnormality in bone formation in ears
  • Dental imperfections

-multiple fractures

(may be confused with child abuse)

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37
Q

Alport syndrome

A

-X-linked disease > patients usually male

Type 4 collagen abnormal > BASEMENT MEMBRANE ! (type 4> floor)

Dysfunction of the:

glomerular basement membrane

Cochlea of the ear

lens of the eye

(Also neural deafness and eye disorders _

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38
Q

describe what this is? and exaplin its macroscropic appearence

A

parenchymal nodules> containing hepatocytes with fibrotic bands in btw

Nodularity> result from hepatocytes regeneration and scarring

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39
Q

Find out what numbers I, 2 and 3 refer to.

With reference to these numbers, in which direction does blood flow in the lobule?

Which area therefore do you think is most susceptible to ischaemic damage?

A

Oxygenation Zones within a liver acinus

Zone 1> closest to vascular zone

Zone 2> intermediate

Zone 3> furthest

Zone 3 is most susceptible to ischaemic damage as it is the furthest from the oxygenated arterial supply

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40
Q

this is a microscopic slide of a cirhottic liver, describe its microscopic feautres

A

blue area> sclerosis around central vein

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41
Q

what is cirhossis?

causes?

A

Cirrhosis is Irreversible scarring of the liver caused by continuous long-term liver damage.

Scar tissue replaces healthy tissue in the liver + prevents the liver working properly.

Causes: ABCDEF

Alcohol

B hepatits

C Hepatits

Drugs

Ethanol

Fe overload (hemochromatosis)

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42
Q

pathogenesis of Cirhossis

A

***Cirhossis> balwa in the space of dissse***

(normally type 1 & 3 collagen r in> portal tract and around central vein, while collagen 4> is in space of disse)

in Cirhossis>> Collagen 1 & 3 r in space of disse!!

Hepatocytes r injured>kupffer cells activation> releases cytokines that allow stellate cells to change and r constantly active>secrete TGF-B> becomes highly fibrogenic & myofibroblast-like> besides laying down collagen and scar tissue in the space of disse, due to their myofibroblast talent, these cells r contracting and increased vascular resistence! alllll of this will contribute to compressing the sinusoids!

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43
Q

Complications of Cirhossis

A
44
Q

Clinical feautures of cirhossis

A

Arise due to portal hypertension or promblems with liver function itself

45
Q

Fat embolism

pathophysiology

presentation

A

after trauma or liposuction.

when a bone is fractures, bone marrow fat cells that r injured break up and realease oil droplets. these oil droplets stick together & r sucked into the ruptured veins.

  • (Respiratory & neurological symptoms)*
  • breathless, madness*

can reach to the brain!

mostly seen in those with pelvic or long bone fracture!

or sometimes it doesn’t have to be due to long bone, it can be bc of a biochemcial abnormality, theres a depostition of fat in the blood.

46
Q

what is DVT?

Pathophysiology

Predisposing factors

Can DVT be treated and prevented?

A

A blood clot that develops within a deep vein in the body, usually in the leg.

predisposing factors

– immobility/bed rest

– post-operative

– pregnancy and post- partum

oral contraceptives

– severe burns

– cardiac failure

– disseminated cancer

Treatment:

1) give IV heparin (doesn’t really dissolve thrombus, but prevents it from getting bigger) (helping it)
2) oral Warfarin **starts with heparin (bc it starts quickly)

Prevention

1) give stockings> they compress veins to prevent stagnation

2) flowtron boots> they inflate, activating muscle calf pump!

47
Q

Pulmonary thromboembolism

Presentation

Pathophysiology

Risk factors

A
48
Q

Air embolism

Pathophysiology

A

An air or gas embolism is a bubble that becomes trapped in a blood vessel and blocks it.

Decompression sickness (a form of gas embolism) = occurs when ppl experience a sudden decrease in atmospheric P.

When air is breathed out at high p. (during deep see dive) increased amounts of gas (mostly nitrogen) is dissolved in the blood & tissues.

when divers ascends (depressurizes) too rapidly!> the nitrogen comes OUT of the solution and into the blood!

49
Q

Amniotic fluid embolism

Pathophysiology

***Extra: why can it cause DIC?

A

During delivery, c- section, a tear in the amniotic membrane can occur and amniotic fluid can get into the maternal circulation.

ARDS, hypotension, seizures, loss of conciousness, DIC

(bc amnionic fluid has prothrombotic substances)

50
Q

Colorectal carcinoma

  • Predisposing factors
  • Presentation
  • Macroscopic and microscopic appearance
  • Principals of staging
  • Tumour marker
  • Screening program
A
51
Q

Uterine leiomyomata

  • Presentation
  • Macroscopic and microscopic appearance
A
52
Q

Osteosarcoma

  • Presentation (location)
  • Macroscopic and microscopic appearance
A

a cancer type of cancer that starts in the bones

a malignant mesenchymal tumor where the cencerous cells produce bone matrix

sarcoma=mesenchymal origin

–>mostly in metaphyisis of long bones, around the KNEE

Macroscopic: codmann’s triangle or sunburst pattern on xray (from elevation of periosteium)

coarse, gritty, gray and white lacelike pattern od neoplastic bone

treat w/ chenotherapy

53
Q

decribe the term for this finding, what disease is is associated with

A

onycholysis

separation of the nail plate from the underlying nail bed

psorasis!!

54
Q

Chronic lymphocytic leukaemia

  • What it is
  • Presentation
A

B cells live too long beyond their life span>> many abnormal B lymphocyte wbc>> lymphocytes look normal under a microscope, but are abnormal as they do not function properly.

55
Q

Malignant melanoma

  • Predisposing factors
  • Presentation
  • Macroscopic and microscopic appearance
A
56
Q

Pancreatic adenocarcinoma

  • Macroscopic and microscopic appearance
  • Complications
A
57
Q

Well differentiated neuroendocrine tumour

(carcinoid tumour)

  • Presentation
  • Complications
A
58
Q

what is sarcoidosis?

A

Sarcoidosis is a rare condition that causes small patches of red and swollen tissue, called granulomas, to develop in the organs of the body. It usually affects the lungs and skin.

The symptoms of sarcoidosis depend on which organs are affected, but typically include:

tender, red bumps on the skin

shortness of breath

a persistent cough

59
Q

Describe how amniotic fluid embolism occurs & the symptoms it can cause.

how can it cause DIC?

A

During delivery, ceserian section, a tear in the placental membrane or rupture of uterine veins & amniotic fluid can get into the maternal circulation.

ARDS, hypotension, seizures, loss of conciousness,

DIC

(bc amnionic fluid has prothrombotic substances)

60
Q

just for fun lalls,

a more chronic form of decompression sicjness is_-___

A

Chaissans disease: persistance of gas emboli in the skeleteal system leads to multiple foci of ischemic necrosis>>

more common istes r at the tibia, femoral heads, humerus

61
Q

What is Barrett’s oesophagus?

cause?

complication ?

A

Metaplasia of oesophageal stratified squamous epithelium to gastric glandular or intestinal type epithelium w/ Goblet cells

Cause: due to chronic acid reflux esophagitis (GERD) , that occurs w/ a hiatus hernia

Complication: asssociated with ^ risk of adenocarcinoma

ur esophageous doesnt like that reflux and decides to change its identity) :P

62
Q

What r these findings of?

A

Osteosarcoma

the periosteum here has been lifted, has laid down a proximal traingular shell of bone known as Codmans triangle 🔺

63
Q

name this condition

A

anthracosis: aysymptomatic condition dound in many urbna dwellers exposed to sooty air

64
Q

what is traumatic myositis ossificans?

A

if use had a traumatic injury, and u start to exersize and go back to what u were doing tooo soon……..

fibroblasts can undergo metaplasia into osteoblasts! SHIITT and can produce bone IN THE FREAKING MUSCLE! this is reversible with rest

65
Q

A 23 year old man is involved in a car accident in which his right leg is fractured in three places. He is immobilised in bed, because of other injuries for three weeks. The leg is in plaster for ten weeks, and he cannot weight-bear.

What changes can occur to his leg due to the immobilisation, and why?

A

Skeletal muscle atrophy (atrophy of disuse) due to a decrease in cell and tissue size. This is the result of decreased functional demand/workload.

Osteoporosis of disuse as a result of increased bone resorption. This is as a result of lack of mechanical stress on the bone.

66
Q

What conditions can occur as a result of prolonged immobilisation?

A

  • Decreased pulmonary ventilation, atelectasis and pneumonia.
  • Thromboembolism.
  • Pressure sores.
  • Skeletal muscle atrophy
  • Osteoporosis of disuse
67
Q

Benign prostatic hyperplasia (BPH)

macroscopic appearnece

complications

treatment

A

increase in size of the prostate gland occurs during aging.

occurs in periutheral zone and presses on the urethra and partially obstruct the flow of urine,

Macroscopic: smooth, elastic, firm nodular enlargment

Complications:

  • bladder outflow obstruction.
  • urinary tract infection (UTI)
  • acute urinary retention
  • Bladder muscle hypertrophy
  • Bladder distension

Symptoms:

  • nocturia or dysuria
  • difficulty starting & stopping urine
  • urge to urinate

Treatment

A1-antagonist> relaxes smooth muscle (terazosin, tamsulosin)

**does not cause cancer!

68
Q

Left-ventricular hypertrophy

Causes

complication

A

enlargement and thickening (hypertrophy) of the walls of ventricle

LVH can occur when some factor makes your heart work harder than normal to pump blood to your body:

  • aortic stenosis
  • hypertension
  • Hypertrophic cardiomyopathy
  • athletic training

complications:

  • can compress on its own blood supply
  • HF
  • arrythmeia
  • atrial fibrillation
  • IHDaortic root dilation
  • cardiac arrest
  • stroke
69
Q

Psoriasis

Which areas of the body are commonly affected?

presentation

macro and microscopic appearence

pathophysiology?

A

Thickened Stratum Coreum with a highly proliferative epidermis and thickining (acanthosis)

Commonly seen in> The skin of the elbows, knees, scalp, ears, lumbosacral area, intergluteal cleft and the glans penis.

Macroscopically – papules, pink to salmon-coloured plaques covered by loosely adherent scales which are silver/white in colour.

Microscopically – acanthosis & parakeratosis w/ a low or absent granular layer.

  • microabscesses of neutrophils .
  • The epidermal rete are elongated and clubbed.
  • thinning of the epidermis over the dermal papillae w/ dilated blood vessels within the papillae
  • Pinpoint bleeding points when the psoriatic scale is scarped off.

Pathophysiology:

Psoriasis is a T cell-mediated disease (CD4+ and CD8+) with increased keratinocyte proliferation.

unknown antigen > triggers T cells > produce GF for keratinocytes & induce them to proliferate at approximately 10x the normal rate!!

Psoriasisssss> ssscaly, microabsseeesss

70
Q

psorasis.

A
71
Q

Apart from the skin which other parts of the body can be affected by psoriasis? (2)

A
  • Nails
  • Psoriatic arthritis

(They can show yellow-brown discolouration (‘oil-slick nails’), pitting, dimpling, separation of the nail bed (onycholysis), thickening and crumbling.)

72
Q

Ovarian teratoma

Presentation

Macroscopic and microscopic appearance

A
73
Q

shrinking of the frontal and temporal anterior lobes of the brain.. (Frontotemporal dementia)

name the disease

A
  • picks disease.
74
Q

a women has been taking prednisone for a yr in order to ensure that she doesnt have an a asthma attack,

what change could be seen in her adrenal glands & why?

A

Atrophy

cuz the best way to shute doen and atrophy an endorcrone gland is to give it doses of its own hormones!

the administration of glucocorticoids

ex: Prednisone, can suppress the hypothalamic-pituitary-adrenal-pathway!

the resulting drop in ACTH levels will cause the adrenal glands to atrophy!

75
Q

what is a hernia?

what is hiatus hernia?

A

Any time an internal body part pushes into an area where it doesn’t belong,

it’s called a hernia.

is when part of the stomach squeezes up into the chest through an opening (“hiatus”) in the diaphragm.

76
Q

What is GOUT?

A
77
Q

Peripheral vascular disease

  • Role of atherosclerosis
  • Presentation/symptoms
A

affecting blood supply to legs due to atheroscleotic plaque!

  • intermittent claudication> pain in calf when walking
  • leriche syndrome>Pain that radiates to back of hips and buttocks.
  • ischemic rest pain
  • Gangrene
78
Q

Describe the finding of this angiogram

A

theres a gap in the left iliac artery, meaning there is a blockage! but u can see collateral circulation developed!

79
Q

Abdominal aortic aneurysm

  • Role of atherosclerosis
  • Complications
A
80
Q

Bowel ischaemia

  • Role of atherosclerosis
A
81
Q

Transient ischaemic attack (TIA) and cerebrovascular infarction

  • why does it occur?
  • Pathophysiology
A

a ‘mini’ stroke

u get neurological symptoms similar to that of a stroke!

BUTTTT they resolve w/ in 24 hrs!

Usually secondary to microemboli originating from the heart or carotid or vertebral arteries.

Cerebral infarction= symtoms dont resolve w/ in 24 hrs!

82
Q

What is a cerebral stroke?

A

A rapid onset of cerebral deficit (usually focal) lasting more than 24 hours or leading to death,

with no cause apparent other than a vascular one.

83
Q

Distinction between ischaemic and haemorrhagic stroke

One risk factor is particularly common in haemorrhagic stroke. What is it?

A

Ischemic= A stroke due to reduction or cessation of blood flow to a localised area of brain due to arterial occlusion or hypoperfusion.

Haemmorrhagic= A stroke due to to bursting of a bv

Hypertension!

84
Q

Heterozygous familial hypercholesterolaemia

  • What it is
  • Consequences
  • clinical signs
A

defects in the LDL receptor > decreased hepatic uptake of LDL and therefore increased circulating LDL

  • tend to have MI before age of 20!!!
  • “my family did not receive the RECEPIT to the butter”*
85
Q
A
86
Q

A 74 year old woman describes an episode of weakness in her right arm which lasted about a minute. Afterwards she returned to normal. She is a smoker and has a history of hypertension.

What is the likely diagnosis?

A

Transient ischaemic attack (TIA).

87
Q

What is a berry aneurysm?

Are these usually due to atherosclerosis?

Where do they tend to occur and where does the blood accumulate after they rupture?

A

A common form of intracranial aneurysm.

No, they are congenital or secondary to blood vessel injury.

circle of Willis and the adjacent arteries.

After rupture the blood accumulates in the subarachnoid space.

88
Q

what is arotic dissection?

A

inner layer of tunica media tear! open and blood enter the tear,

this seperates the media into 2 layers!

89
Q

What is this

A

Erythema nodosum

is a type of panniculitis. Panniculitis occurs when there is inflammation of the layer of fat lying underneath the skin. The inflammation causes red rounded lumps (nodules) to form just below the skin surface, which are tender. Erythema nodosum most commonly affects both shins.

90
Q

A 67 year old woman presents with fever and lower abdominal pain.
She has an abdominal ultrasound scan and a sigmoidoscopy. A
diagnosis of diverticular abscess is made. She has a BMI of 32 kg/m2
and has a history of hypertension, diabetes mellitus, chronic
obstructive pulmonary disease and rheumatoid arthritis. Her
medication consists of frusemide, metformin and prednisolone. She
undergoes a sigmoid colectomy.

a) This patient has three risk factors for poor healing. What are they?

A

 Obesity

 Diabetes mellitus

 Treatment with steroids

91
Q

What are abdominal adhesion?

A

Bands of fibrous tissue that form between abdominal tissues and organs

92
Q

Chronic cholecystitis

microscopic and macroscopic appearence

A
93
Q

Kaposi’s sarcoma

what is is

what causes it?

A

Kaposi’s sarcoma is a rare type of vascular tumor cancer caused by a virus.

94
Q

Xeroderma pigmentosm

genetic changes

presentation

A

Xeroderma pigmentosum (XP) is a rare, autosomal recessive disorder. There is an impairment of the skin’s ability to repair damage from ultraviolet (UV) light,

🌞🌞🌞🌞🌞🌞🌞🌞🌞🌞🌞🌞🌞🌞

The main presenting features of XP are photosensitivity, skin changes and a high incidence of skin cancer and 👁 damage at a very young age. Skin changes occur first over the areas most exposed to light, initially on the face.

XP is an autosomal recessive genetic condition caused by alterations (mutations) in 9 different genes.

>> Eight of the genes make up the nucleotide excision repair pathway (NER) that identities and repairs UV induced DNA damage. The ninth gene acts to bypass unrepaired damage.

95
Q

Excessive alchohol intake

Effects on liver?

Lab?

A

causes fatty liver, mallory’s hyaline accumalated in hepatocytes

96
Q

What is a traumatic neuroma? What symptoms might it produce?

A

A disordered proliferation of axons resulting in a tangled mass

97
Q

Hepatitis B

Presentation?

Lab findings?

A

Hepatitis can be classified as acute or chronic. Chronic hepatitis is defined as over 6 months history with histology of inflammation and necrosis.

Laboratory diagnosis:

Raised serum ALT, AST and LDH. These are cytosolic hepatocellular enzymes and their presence in the blood indicates poor hepatocyte integrity.

Raised bilirubin (often conjugated) – indicates poor biliary excretory function.

Decreased albumin, raised PT (reliant on factors 2,7,9,10 produced by the liver), raised ammonia – these findings indicate poor hepatocyte function.

98
Q

Acute pancreatitis

Lab?

A

Raised serum amylase in first 24 hours.

Raised serum lipase from 72-96 hours.

In 10% see glycosuria.

Hypocalcaemia possible – due to precipitation of calcium salts in fat necrosis

99
Q

Hereditary Haemochromatosis:

A

What it is – Genetically disorder resulting in increased intestinal absorption of dietary iron Presentation – may be asymptomatic, or present with multiple-organ-related symptoms

Complications - liver damage, heart dysfunction and multiple endocrine failures, especially of the pancreas, arthropathy, hypogonadism

Treatment – Therapeutic phlebotomy (bleed the buggers)

100
Q

Acute Appendicitis

Macroscopic

Microscopic

Causes?

A

lymphoid follicles r collection of lympohcytes that get to their maxium size in the appendix during adolecense.

if infection occurs> the immun esystem ramps up and the follicles can grow!

101
Q

Appendicitis

Complciaiotn?

A

the appendix can keep on swelling and eventually compress on the surrounded blood vessels causing Ischmeia!

increased pressure causes the appendix to burst and rupture and the Pus leaks out c=and goes into the perotineal cavity

Sepsis, abscess, peritonitis

102
Q

Why does the inflamed appendix (in appendicitis) appear plumper than normal?

why do u get abdominol pain

A

the appendix is always secreting mucos like the instestines.

when it gets obstructed, the mucos accumalates and compresses on agencent visceral nerves leading to>> abdominol pain

103
Q

meningitis

shnu ahwa?

complications?

A

Meningitis is an acute inflammation of the protective membranes covering the brain and spinal cord, collectively known as the meninges.

  • Raised intracranial p>> death
  • Septecemia
104
Q

Macroscopic appearnece of meningtis in brain

Given the anatomy of the skull, what effect might this have?

A

Sulci cant be seen due to the filling of the lines by Purulent exudate pus, due to acute inflammation.

Compression of the brain because the skull is rigid.

Raised intra cranial pressure

105
Q

What organisms commonly cause meningitis in the following age groups?

Neonates:

Children:

Young Adults:

Older age groups:

A

Neonates:

Group B strep, organism acquired from the mother. Usually during a UTI. E Coli, Streptococcus pneumonia

Children:

Strep pneumonia, Group B streptoccus

Young Adults:

Menogococal meningitis, Strep. pneumonia

Older age groups:

Streptococcus pneumonia

106
Q

Ascending Cholangitis

~link w/ gall stones

common causative organisms

complicatons

A