mrcp part 1 Flashcards
(283 cards)
quinolones mechanism of action
inhibit topoisomerase II (DNA gyrase) and topoisomerase IV
most common cause of viral meningitis
human enteroviruses- coxsackievirus/ echovirus
specificity
people who DO NOT have the disease and test NEGATIVE
TN/ (TN + FP)
sensitivity
people who HAVE the disease and test POSITIVE
TP/ (TP + FN)
mechanism of action of cisplatin
can cause cross linking in DNA
( CC- Ciplatin= Crosslinking)
Mechanism of action of vincristine
inhibits microtubules formation
positive predictive value
the chance the person has the disease if the test is positive
PPV= TP/ (TP +FP)
negative predictive value
the chance the person DOES NOT have the disease if the test is NEGATIVE
NPV= TN/ (TN + FN)
Burkitts lymphoma gene
c-myc gene translocation
normallt t(8;14)
receptor for EBV
CD21
(21 year olds can get EBV)
treatment for widened QRS in tricyclic overdose
IV sodium bicarb
Loffler’s syndrome
Transient respiratory illness (fever, cough, night sweats) causing blood eosinophilia and CXR shadowing.
Can be caused by parasites
Treatment for acute eosinophilic pneumonia
highly responsive to steroids
secondary messenger system stimulated by NO
cGMP
Action of proteasome
Degredation of polypeptides through breaking polypeptide bonds
Found in nucleus and cytoplasm
Von Hippel-Lindau method of inheritence and location of gene
Autosomal dominant
VHL gene on chromosome 3 (VHL=3letters= chromosome 3)
Von Hippel-Lindau associated tumours
cerebellar haemangiomas–> subarachnoid haemorrhages
retinal haemangiomas–> vitreous haemorrhage
renal cysts (premalignant)
phaeochromocytoma
extra-renal cysts: epididymal, pancreatic, hepatic
endolymphatic sac tumours
clear-cell renal cell carcinoma
Cancer associated with Hashimotos
MALT tumours
can present without typical B featuresf
CLL treatment regime
FCR
Fludarabine cyclophosphamide rituximab
Non Hodgkins lymphoma treatment
RCHOP
Rituximab doxorubicin cyclophosphamide vincristine
Gene defect in AIP Acute intermittent Porphyria
Porphobilinogen deaminase
Aip- porphobilinogen deAminase
Gene defect in PCT porphyria cutanea tarda
uroporphinogen decarboxylase
pCt= uroporphinogen deCarboxylase
investigation for betathalasaemia trait
haemoglobin electrophoresis
causes of upper zone fibrosis
C - Coal worker’s pneumoconiosis
H - Histiocytosis/ hypersensitivity pneumonitis
A - Ankylosing spondylitis
R - Radiation
T - Tuberculosis
S - Silicosis/sarcoidosis
Think up in the charts