PPQ Imp Flashcards
What is the most common parasitic infection in the duodenum causing malabsorption?
Giardiasisi Duodenalis
40 year old,with low TSH and very high T4, what sign would you likely see in/around her eyes if you look closely?
Periorbital myxoedema/
If phrased differently think about Exophthalmos
What are the vaccines that are offered in pregnancy?
Influenza, Whooping cough and Covid
What is the method to help reduce the chances of acute ABO rejection in the transfer of an ABO incompatible kidney?
Plasmaphoresis
Apparently Hyperacute doesnt have a treatment?
As prevention plasmophoresis
Hospital is low on O- what is the most approapriate method to give blood who comes in as a casualty?
Give O+ if male or female who can’t get pregnant
If there is a patient with poorly controlled diabetes and an eye infection that is oozing, What is the most approapriate immidiate pharm Tx?
The diagnosis is Mucormycosis
Treated by Amphotericin B
Patient has joint pain and a rash. She has an autoimmune condition what is it called? Results show a reduced C1q
SLE (Systemic Lupus Erythematosus)
Man has intermittent mouth and tongue swelling for 2 years. This is unresponsie for over the counter anti-histamines. He is also on Aspirin and ACE inhibitor. what is the most likely cause?
Drug induced reaction
A woman has mouth and lip swelling following a dental procedure, and her mother reports a similar problem in the past?
C1 esterase inhibitor deficiency
Heridatory angiooedema
What is the genetic mutation in digeorge syndrome?
22q11.2
What natural antibody is protective against HIV?
HIV-gp120
gp41
What allergy is more likely to present in a child?
Egg
What is the Maintanence treatment against allograft rejection?
Induction agents are?
MAINTANENCE :Mycophenolate mofetil/Azath +pred + Tacrolimus
INDUCTION : OXT3/ATG, anti-CD52, anti-CD25
§ Given at time of transplantation or just before to prepare the patient to receive the foreign organ
What is the mechanism of hyperacute allograft rejection?
This where antibodies are against HLA or ABO
These antibodies are preformed and occur within an hour of transfusion
What is the effect of gene mutation in Familial mediterranean fever?
There is a mutation in MEFV and this causes a problem in the pyrin-marenostrin which then leads to increased IL-1, NF kappa B and apoptosis
What type of hypersensitive causes serum sickness ?
This is a type 3 complex mediated hypersensitivity
What infections are covered by conjugate vaccines?
Encapsulated infections.
Pneumococcal vaccines or Hib vaccines
What does PD-1 inhibit
T-cells
Nivolumab is an example and treats Malignant melanoma
cAnca with glomerularnephritis and lung changes what does he have
Wegner;s or granulamatosis with polyangitis
Rituximab which acts on CD 20, effects what cell type?
B-cells.
What is the max number of HLA mismatches?
What if this is between mother and son
So max mismatch is 6
Mother and son max is 3
What condition is NOD2/CARD15 associated with?
Crohn’s disease
What is the receptor /cytokine mutation that can be protective in HIV?
CCR5/MIP-1a or b
What is found in coeliac biopsy?
Crypt hyperplasia
Non-caseating granuloma
Intraepithelial lymphocytes
I think Villous atrophy as well
Chimeric antigen receptor T-cell (CART) therapy Cd19: What type of haematological malignancy foes it target?
ALL and some non-hodgkins lymphomas
Multiple myeloma
Mantle cell lymphoma
CART therapy essentially creates T-cells that search for C19 cells which are B-cells therefore targeting them
Pleuritic chest pain, joint pain, positive ANA and Anti SM but there is no abnormal liver enzyme derangement, raised ESR. what is the likely diagnosis?
SLE (Systemic Lupus Erythematosus)
For the treatment of ankylosing spondyitis, NSAIDs TNF inhibitor have been tried what else can be targeted?
IL17
What is the mechanism of graft versus host disease?
presentation?
prophylaxis
Treatment
Donor T-cells react to host cells
??CD4+ activated and assists CD8+ and B cells
Presentation is Days-weeks –> N+V, bloody diarrhoea, abdo pain and jaundice
Methotrexate /cyclosporin prophylaxis IRRADIATE BLOOD
Treated with steroids
What virus causes progressive multifocal leukoencephalopathy?
John cunningham virus
What condition is a complication of the John Cunningham virus?
The JC virus causes progressive multifocal leukoencephalopathy
Diffuse large B-cell is lymphoproliferative disease caused by this virus
Autoimmune hypothyroidism (Hashimoto’s is associated with which antibody)
Anti thyroglobulin
What is dry eyes and parotid sweling associated with (antibody)?
Diagnosis
Anti-ro and anti la (Which are both Anti ENAs)
Sjrogrens syndrome
Swollen joinst of the hand and X-ray showing erosive changes antibody
Anto CCP
What is the treatment of Osteoperosis? (When bisphosphonates are not tolerated)
RanK L -> Denosumab
What is the treatment for Chronic granulomatous diase?
IFN gamma
Which immune cell is produced in the bone marroe and then migrated to ht site of injury. It has oxidative and non-oxidative killing abilities and dies when the job is done?
What will they be if after they did their jobs they would ace as APCs
Neutrophils
The APCs would be Macrophages
Foxp3+ And CD25+ cells, they mature in the thymus
Treg cells
What immune cells detects antigen in the periphery and moves to lymph nodes
Dendritic Cells
What immune cell detects MHC1 and kills virus infected/cancer cells. Is inhibited by MHC I
NK cells or CD8+ cells
NK cells -> MHC 1 inhibition
When infected or cancerous loose some MHC 1 and so loose the inhibition
CD8+ recognise abnormal MHC1 antigen presentation leading to them attacking the cell
I think
What immune cells is targeted by HIV
Memory CD4+ ccells
Sle with recurrant clotting
Diagnosis
Antibody
Phospholipid syndrome
Anti cardiolipin
72 year old women with stiff limb girdles. Aches all over and joint stiffness
Diagnosis
Antibody
Polymyositis? - Anti Jo 1 or anti srp
Polymyalgia rheumatica -> Most representative of symptoms imo but not really associated with antibody
Rheuamtic arthritis –> AntiCCP –> More likely than polymyositis current thinking
polymyalgia rheumatica mainly refers to the shoulder girdles, not peripheral joints - if there’s peripheral joint involvement more likely RA –> BENJI
CREST syndrome antibody
Anti-centromere
(EMQ) A teenage girl who when she goes cross country running gets an erythematous rash on her legs. It is well controlled by antihistamines
Diagnosis
Cold urticaria
(EMQ) Man can eat apple pie. But if he eats fresh apples and pears, he gets inflamed lips
Oral allergy syndrome
(EMQ) Man has an allergic reaction during surgery and who’s lips becomes swollen/oedematous when blowing up balloons as his daughter’s birthday party
Type 1 hypersensitivity latex allergy
(EMQ) Bloated after drinking milk but not IgE mediated
Lactose intolerance
(EMQ) A girl with a sore throat is given penicillin and develops a rash. She is found to have EBV
Drug reaction
(EMQ) What cells do Myasthenia gravis antibodies bind to?
They bind to skeletal muscle
(EMQ) What will be measured in a patient with well controlled HIV, who is currently on HAART?
Lymphocyte subset
A woman with known SLE presents with an exacerbation of her SLE/ worsening symptoms, what would you measure?
C3 and C4
A 60 year old lady with recurrent chest infections now has reduced total serum protein and has autoimmune thrombocytopenia
Common variable immunodeficiency
A 12 year old boy has recurrent chest infections and has an ear infection. He doesn’t have any B Cells
Bruton’s Agammaglobulinaemia
Boy with recurrent abscesses has a negative NBT test
Chronic granulomatous disease
A Girl is found to have no CD4 cells, but CD8 cells and B cells are present
Bare lymphocyte syndrome 2
A boy’s father has TB. The same boy develops a mycobacterium infection, following their BCG
What is their primary immune deficiency
Interferon gamma receptor deficiency
Young boy with normal B cell numbers and absence of CD8+ and CD4+
They have a deficiency in the common gamma chain protein
X-linked SCID
Normal B and T cells, high IgM but absence of IgA, IgE and IgG
Hyper IgM syndrome
Encampsulated bacteria infections that are recurrent suggests what primary immune deficicencys
Complement deficiency e.g. C7
Either the complement deficiency alternate or common
What is used to treat lymphoma and rheumatoid arthritis
Rituximab
What is used to prevent transplant rejection by blocking T cell activation
Tacrolimus or Cyclosporin
What is used to treat severe ankylosing spondylitis not controlled by NSAIDs.
etanercept (Anti-TNF alpha)
1st NSAIDS
2nd Anti TNF alpha
3rd Anti 1l 17
Monocytes found in the tissue are called
Macrophages
Liver - Kupffer cells
What is the name of the differentiated B cells that produce immunoglobulins
Plasma cells
What condition is associated with DR4 and CCP
Rheumatoid arthritis
What is the condition that is associated with a mutation in the FAS pathway, with lymphocytosis, lymphomas and autoimmune cytopenia
Autoimmune lymphoproliferative syndrome
ALPS
A woman with periorbiital purple rash and rash on knees, which enzyme is elevated?
Grotton’s papules - Red violet bumps outside joints of the hand
Creatine kinase (dermatomyositis)
Within muscle → perivascular CD4 T and B cells
o Immune complex mediated vasculitis – T3 response
What virus can lead to post traplantation lymphoproliferative disease?
Epstein barr virus diffuse large b cell lymphoma
Patient presents with clear discharge from the nose every summer. These symptoms seems very allergic like. What is the cause?
Allergic rhinitis
A diabetic patient with Hypertension is being treated, and develops angioedema.
What is the cause?
This is a drug reaction to ACE inhibitor?
What zoonotic disease does Ixodes Tick cause?
Lyme disease
What is the main class of drugs that are used to treat HIV?
Nucleoside reverse transcriptase inhibitor
What is the amyloid that is deposited in multiple myeloma and what type of amyloidosis is this?
Amyloid light chain amyloidosis which is a primary amyloidosis?
What is Behcet’s Disease?
Epi
Pres
Some of the other symptoms
Systemic Vasculitis of unknown cause
This is a multisystem disorder of the small, medium and large sized blood vessels.
Epi- Easter Mediterranean mainly in men 20-40 yrs
PRESENTATION
Cant see, cant pee and cant eat spicy
Anterior uveirtis
Genital ulcers
Oral ulcers
What is Polyarteritis Nodosa?
Cause
Presentation
Ix
A vasculitis affecting the medium sized vessels.
Aetiology: Idiopathic / Hep B infection
Presenation:
- Renal -> HTN + Renal failure
- Abdo: Abdo pain
- Skin: Livedo reticularis
- Nerves
- Arthralgia
- Systemic Flaws
Investigations:
CTA/MRA: ROSARY SIGN
Takayasu’s Arteritis
What is it?
Presentation? (6)
Associations?
Treatment?
- Large vessel vasculitis.
- Typically occludes the aorta and questions commonly refer to an absent limb pulse.
- More common in females and Asian people.
Features
- Systemic features of a vasculitus e.g malaise, headache.
- Unequal blood pressure in upper limbs
- Carotid bruit
- Intermittent claudication
- Aortic regurg
Associated with renal artery stenosis.
Manage with Steroids
Which vasculitis causes a disease in a branch of the external carotid artery?
This is a large vessel vasculitis and so is probably Giant cell arthritis
Takayasu arthritis is possible but more rare.
Man with cough, SoB and weight loss. Hyponatraemia, low serum osmolality, urine Na and osmolality were inappropriately normal, what is the cause of the low sodium?
SIADH secondary to small cell lung carcinoma
Elderly woman with C. diff colitis and profuse diarrhoea, Presents with low sodium, what type of hyponatremia will be present?
Hypovolaemic hyponatraemia
Man who has been in a car accident, raised sodium and plasma osmolality, low urine osmolality
Cranial Diabetes insipidus
There is a raised Na and a low K but there is a raised Renin, What is the cause of this presentation
Renal artery stenosis.
Could have been hyperaldosterone but the raised renin tells us it is renal artery stenosis.
What are the indications for dialysis?
A - Acidosis pH<7.1
E - electrolytes - Refractory Hyperkalaemia
I - Intoxification/Ingestions Toxic alcohol, salicylates, lithium
O - Overload - Congestive heart failure
U - Uraemia - Uremix pericarditis and uremic encehaloppathy
What is described by true positives divided by the total number of people who have the disease describe?
Sensitivity
What is the true negative divided by the total number of people who don’t have the disease describing?
Specificity
What is described by the people who are true positive divided by the number of people who tested positive?
Postive predictive value
What is described by the people who are true negative divided by the the number of people who tested negative?
Negative predictive value
What ion is likely to be outside the normal range in an alkalotic picture?
K+
Na+
Ca 2+
Mg 2+
K+ (I think) It decreaseas
What is the best investigation to confirm cushings disease?
High dose dexamethasone
Apparently inferior pituitary petrosal sinus sampling
A man has gout and is kept up at night by it. His symptoms are relieved by ibuprofen, but when he stops taking it, the symptoms come back. His neighbour is on allopurinol, and he would like to be on it too. Which of these medications would need to be altered for them to be able to be prescribed allopurinol?
Azathioprine
Azathioprine is a powerful immunosuppressant drug used in the treatment of inflammatory bowel disease and other conditions.
{{c1::Thiopurine methyltransferase (TPMT)}} deficiency is a congenital deficiency in an enzyme used to convert 6-mercaptopurine, a breakdown product of azathioprine, into less toxic, excretable metabolites. Approximately 1 in 300 people are deficient.
There are only two ways the body can clear 6-mercaptopurine: {{c1::Thiopurine methyltransferase (TPMT}} and the {{c2::Xanthine Oxidase pathway}}.
If a patient is on both azathioprine and allopurinol AND they have {{c1::Thiopurine methyltransferase (TPMT}} deficiency - this leads to a buildup of toxic metabolites that may lead to profound leukopenia and death.
All patients starting azathioprine need {{c1::Thiopurine methyltransferase (TPMT}} levels checked
Be cautious about patients on both {{c3::allopurinol (Xanthine Oxidase inhibitor)}} + azathioprine - have their {{c1::TPMT}} levels been checked?
A person have a pituitary adenoma removed. What is the medication that needs to be provided if they are discharged?
DDAVP
Fludrocortisone
Testosterone
DDAVP
But if hydrocortisone or a a steroid is present choose that one
Ilan said he remebered something about hydrocort, thyroxine then sex steroids depending on gender?
ChatGPT said DDAVP pick whatever you want
Describe the metabolic picture in the most common form of congenital adrenal hyperplasia?
Na
K
volume
Na+ this will be low
K+ Will be high
Hypovolaemia
Most common version is 21 hydroxylase
Low glucose high insulin
What needs to be measured?
C-peptide
Low glucose high insulin High C-peptide
Insulinoma, or Surreptitious gliclazide
What ion is raised in red cell lysis?
K+
What does PCSK9 inhibitor halve?
Evolucumab - halves LDL
Which molecule takes cholesterol and moves it to liver and steroidogenesis organs?
HDL
Look where the L is, HDL (L at the end cause to the liver)
LDL L at the start so from the liver
Vitamin deficiency that causes both megaloblastic anaemia and Neural tube defects>?
Folate
What hormone would be raised in the most common cause of CAH?
Sex Steroid hormones (Androgens)
And
ACTH
What hormone leads to increased levels of prolactin?
What causes a decrease in prolactin?
Increase- Thyroid Releasing hormone
Decrease- Dopamine
What is produced by a medullary carcinoma of the thyroid?
Calcitonin
A man develops signs of hyperthyroidism. Bloods show low TSH and high thyroxine. A technetium scan shows no uptake. What is the likely diagnosis?
Viral thyroiditis/ De Quervain’s thyroiditis
An old man who fell over, been on the floor for days. Severely dehydrated. Dark urine. Not blood on microscopy. What causes dark urine?
What enzyme will be raised?
Rhabdomyolysis leading to Myoglobin
Creatinine kinase
What liver enzyme is raised in an MI?
Aspartate aminotransferase
Could be ALT???
What enzyme is used to confirm cardiac failure?
B-type natriuretic peptide
5yr old, tetany, bone pain. Widened epiphyses + ‘Cupping’ of metaphysis shown on x-ray. What is the cause?
Rickets
Publican with diabetes, fatty stools, weight loss, ‘slate grey skin’ and joint pains. What is the underlying diagnosis causing this?
Haemochromatosis (joint pain, skin changes, pancreatitis, liver deposition)
Swollen joint, needle-shaped aspirate with negative birefringence, which enzyme manufactures the material that makes up the crystals?
Treatment for previous question, specifically one you should use acutely
Xanthine oxidase
Acute: Colchicine or an NSAID
Chronic: Allopurinol or probenecid
T1DM with hypoglycaemia, what is the management option if no IV access?
IM glucagon
Patient with GI conditions, lack of which substance leads to B12 being malabsorbed?
Intrinsic factor
Which thyroid cancer is most commonly metastsisises to the lymph nodes?
Papillary
What is the most common cause of pancreatitis?
Gallstones
GET SMASHED
First three are in order
Gallstones, Alcohol and then trauma
Gallstones is likely if acute pancreatitits,
Alcohol is the answer if it is chronic pancreatitis
What is the best test that will help with the diagnosis of temporal arthritis?
ESR
If asking for gold standard this would be a biopsy. Normally however this cant get an affected part of the vessel so is not helpful
40 y/o woman presents with headache, but normal visual fields. MRI shows a 4mm pituitary adenoma. Investigations:
Cortisol 400 (high end of normal)
ACTH 30 (normal)
Prolactin 1400 (high)
TSH 3.3 (normal)
Free T4 17 (normal)
What is the most likely diagnosis?
Acromegaly
Hypopituitarism
Nonfunctioning pituitary macroadenoma
Prolactinoma
TSHoma
Prolactinoma
40 y/o woman presents with headache and a bitemporal hemianopia. MRI shows a 2cm pituitary adenoma. Investigations:
Cortisol 400 (high end of normal)
ACTH 30 (normal)
Prolactin 1400 (high)
TSH 3.3 (normal)
Free T4 17 (normal)
What is the most likely diagnosis? – same as prev question but with hemianopia?
Acromegaly
Hypopituitarism
Non-functioning pituitary macroadenoma
Prolactinoma
TSHoma
Non-functioning pituitary macroadenoma
40 y/o woman has post-partum haemorrhage and is then unable to breastfeed. Investigations:
Cortisol <50 (very low)
ACTH <10 (very low)
Prolactin <50 (very low)
TSH 0.9 (normal)
Free T4 12 (normal)
What is the most likely diagnosis?
Acromegaly
Hypopituitarism
Non-functioning macroadenoma
Prolactinoma
TSHoma
Hypopituitarism
Which of the following would be consistent with obstructive jaundice?
Normal ALP
Normal AST
Normal GGT
Dark stools
Increased bilirubin in the urine
Increased bilirubin in the urine.
Normally dark urine is because of urobillin. In obstructive jaundice the dark urine is because the bilirubin gets into the urine however.
Which of the following is found in haemolytic jaundice?
Raised AST
Raised CK
Normal bilirubin
Pale stools
High urobilinogen in urine
This is high Urobilinogen in the urine
The liver function is fine and so is the movement of bilirubin in the blood. This means that the normal process can occur leading to more urobillin in the urine.
Calcium high, PTH low
Bone Mets
Could also be Sarcoid, thyrotoxicosis, High Vit D etc
Patient can’t fit in her shoes or put on her wedding ring and has prognathism, what test do you need to do to confirm?
serum IGF then oral glucose tolerance test
BP 190/100, thin skin, overweight, high-normal sodium, low normal potassium, OGTT done (glucose high normal)
low dose dexamethasone suppression test then
inferior pituitary petrosal sinus sampling
Pt with low Na, High K + postural hypotension
Ix?
Addison’s
Therefore SyncACTH test.
Patient with low sodium, potassium normal, low plasma osmolality and urine osmolality was 70
Primary polydipsia,
fluid deprivation test
Women with colicky pain.
Elevated mildly elevated ALP, ALT, GGT, & Bilirubin.
GGT + Bilirubin most raised of results provided.
Gallstones
Acute Cholestasis
Any Post hepatic cause of jaundice probably
A 57 year old man presents following hematemesis and is found to have high ALT + GGT, slightly raised ALP, and low Albumin
Diagnosis
Cirrhosis
An elderly gentleman has massively elevated ALP on its own, and the other results are normal. He also reports a history of headaches.
Diagnosis
Paget’s
What is the bicarbonate level of someone with pyloric stenosis?
High Bicarbonate
Therefore you would expect to see a low potassium, normal sodium and high bicarbonate
PATHOPHYSIOLOGY
You would expect low CL because of vomiting of HCL from stomach.
You would expect an individual to become dehydrated from vomiting. So you would expect the kidneys to respond to dehydration by increasing water reabsorption via Vasopressin/Anti-diuretic hormone and Aldosterone.
Aldosterone allows trading of water in the renal tubules back into the blood in exchange for potassium in the blood. Just like how Insulin allows trading of water from within cells, back into the blood, in exchange for potassium to flow into the cells (from the blood). Another effect of aldosterone on the kidneys (in the renal tubules) is to allow H+ trading into the urine, in exchange for HCO3- from the urine. This results in a metabolic alkalosis (= H+ lost from the blood, and HCO3- reabsorbed into the blood).
Therefore in Pyloric stenosis, the sodium is reabsorbed to draw the water into the body, and result in a high bicarbonate.
What is the K+ level in a patient with DKA?
Raised K+
K+ matches H+ conc most of the time
Man with impaired glucose tolerance fasting value
Between 6.1 and 6.9
WHO criteria for diabetes and blood glucose impairment:
NORMAL fasting glucose (FGP): {{c1::≤6.0}} mmol/L
IMPAIRED fasting glucose (IFP): {{c1::6.1‒6.9}} mmol/L
Diabetes Mellitus: {{c1::≥7.0}} mmol/L
WHO criteria 2-hour glucose tolerance test
Impaired fasting glucose :{{c1::≥6.1 - 6.9}} mmol/L
Normal Glucose tolerance : {{c1::<7.8}}
Impaired glucose tolerance {{c1::≥7.8 -11.0}} mmol/L
Diabetes : {{c1::≥11.1}} mmol/L
Deficiency of which enzyme leads to hyperuricemia?
HGPRT ->
hypoxanthine-guanine phosphoribosyltransferase
This is Lesch Nyhan disease?
Rare inherited disorder that effects the metabolism of purines.
Developmental delay, junenille gout and self mutilation.
What enzyme is raised in Mumps?
Amylase-S or P?
Mumps is associated with Pancreatitis and so leads to an increase in amylase levels.
S stands for salivary gland so it is that one
Baby with seizures: low Ca, low PTH
Primary hypoparathyroidism?
10 year old with seizures: low Ca, high PO4, high PTH
Renal osteodystrophy
Secondary hyperparathyroidism is probably correct, but this would cause a low phosphate or high phosphate depending on the cause. In the cases where the phosphate is high there must be a problem with the kidney leading to the diagnosis of renal osteodystrophy, as opposed to a vitamin D deficiency cause,
Colour blindness is caused by which Vitamin deficiency?
Vit A
What vitamin deficieny causes pellegra?
How does thie condition present?
Niacin / B3
It is associated with Diarrhoea, dementia and dermatitis
DEATH if untreated
What vitamin deficicency is associated with beriberi?
What is the presentation of this? (Wet/Dry)
Vitamin B1/ thiamine.#
Wet - > heart related overload
Dry -> neurological deficits like Wernickes. Pabrinex
A man requires a 6 unit transfusion after a traffic collision, and two hours later becomes
breathless, feverish, and tachycardic
What is the diagnosis?
Transfusion related acute lung injury?
OR
Transfusion associated circulatory overload (MOST COMMON ACUTE REACTION)
What are causes of acute transfusion reaction under 24 hours?
o Acute haemolytic (ABO incompatible)
o Allergic/anaphylaxis –> improvves with antihistamine and hx of atopy/ Often associated with facial swelling
o Infection (bacterial)
o Febrile non-haemolytic –> Will have high temperature during transfusion
o Respiratory
▪ Transfusion associated circulatory overload (TACO)
* Often pre-existing cardiac/respiratory problems
* 1 in 100,000 mortality risk (very preventable)
* MOST COMMON ACUTE REACTION
▪ Acute lung injury (TRALI)
What are the causes of delayed transfusion reactions?
o Delayed haemolytic transfusion reaction (antibodies) – Duffy and Kidd
o Infection (viral, malaria, vCJD)
o TA-GvHD (week or 2 after transfusion)
o Post transfusion purpura
o Iron overload
A thalassemia patient presents with malaise and erectile dysfunction
Transfusion-related
haemosiderosis
A Lady with myelodysplastic syndrome requires regular monthly blood transfusions. 10
minutes after her latest transfusion she becomes tachycardic, has transfusion site pain, and
is hypotensive
ABO incompatibility
ABO incompatibility occurs when the recipient’s antibodies react with the transfused red blood cells that have different ABO antigens. This immune reaction leads to the destruction of the transfused red blood cells and subsequent release of substances that can cause symptoms such as tachycardia, transfusion site pain, and hypotension. AHTR is a serious and potentially life-threatening complication.
While anaphylactic reactions can occur during blood transfusions, they typically present with symptoms such as hives, itching, respiratory distress, wheezing, and significant hypotension. However, anaphylactic reactions are less common compared to AHTR in the context of blood transfusions.
Man feels itchy after transfusion, calms down with cetirizine <24 hrs
Allergic reaction
Alcoholic has an AAA repair and several days later develops a fever, low Hb, and jaundice
Delayed transfusion reaction
Rank the following in the likihood of infection?
RBC
Platelets
FFP
Platelets (room temperature)
RBC
FFP
What temperature is platelets kept in?
shelf life
room temp
22 degrres celc
7 days
What temp RBC storage?
shelf life
4 deg cel
35 days
Platelet levels in pregnancy. Normal vs ITP
Normal > 70 x 10^9
ITP if less than, or some other pathology
Protein S levels in pregnancy?
decreased
A woman after placental abruption and surgery has:
low fibrinogen, prolonged APTT,
prolonged PT
DIC
Bascically every clotting thing will be fkd
Which test is used to detect beta thalassaemia ?????
High performance liquid chromatography
OR
Electrophoresis (Gold standard)
there will be raised Alpha globulin because of less beta globulins being created (NOT SUREEEE)
What tumour is associated with Pseudomyxoma peritonei?
Mucinous tumour of the ovary