Professional Documents
Culture Documents
-Most of the questions- answers are in the intensive course lecture slides esp physiology of
renal/respi/GI and antibiotics and organisms-so really need to study the slides. Only a few anatomy
questions.
-transitional cell
-spinothalamic (no lateral spinothalamic as answer choice). (Answer has lateral corticospinal to
confuse you).
7. Pseudomonas antibiotics:
-cefipime
- E. Coli
9. Clamydia antibiotics
- doxycycline
10. Gas gangrene organism and antibiotics : clostridial, penicillin and clindamycin, most
common Clostridium perfringens. Clostridium perfringens, Clostridium septicum, and Clostridium
histolyticum. C. septicum
- tertiary bonchus
- posterolateral
- supraspinatus
- pretracheal (thyroid)
- opthalmic nerve
- fat necrosis
22. PT, aptt, platelet normal; what underyling disease will cause hypercoagubility for the pt ?
Christmas disease ?factor v mutation ?Protein c mutation ?anti thrombin III mutation
https://oxfordmedicine.com/view/10.1093/med/9780190862800.001.0001/med-9780190862800-
chapter-67#:~:text=Definition.,may%20be%20multiple%20factors%20present.
Inherited clotting disorders
1. i. Factor V Leiden mutation is the most common inherited factor associated with
hypercoagulability. This mutation causes resistance of factor V to the cleaving action of
activated protein C.
2. ii. Prothrombin G20210A mutation is the second most common inheritable factor
associated with hypercoagulability and results in an mRNA that has an increased half-
life, leading to elevated levels of prothrombin protein. When coinherited with a factor V
Leiden mutation, patients have a substantially increased risk for the development of a
clot as well as an increased risk for recurrent DVT.
3. iii. Protein C or Protein S deficiency is uncommon but displays a high penetrance for
the occurrence of venous thromboembolism (VTE). These proteins normally function to
reduce levels of factor Va and factor VIIIa, leading to decreased thrombin generation.
Patients with deficiencies fail to properly regulate the coagulation cascade.
4. iv. Antithrombin (or antithrombin III) deficiency is a rare autosomal dominant
disorder with a relatively high level of penetrance for DVT. The normal protein functions
as a protease inhibitor of factor IIa (thrombin) and factor Xa Its activity is modulated by
heparin, leading to the basis of its clinical use. Deficiencies in antithrombin lead to
dysregulation of the clotting cascade.
5. v. Rare disorders include dysfibrinogenemia, plasminogen deficiency, heparin cofactor
II deficiency, factor XII deficiency, and elevated clotting factor levels.
-facial nerve
24. Midshaft humerus fracture nerve involved
- radial nerve
- Pt undergoing TURP
37. Immediately after birth what will happen- closure of foramen ovalae
38. Blood supply for brain visual field - posterior cerebral artery
from the facial veins (via the superior and inferior ophthalmic veins) as well
as the sphenoid and middle cerebral veins
44. Oral contraceptive pills causing liver tumour type- liver adenoma.
50. How renal compensatory reabsorp hco3 , which channel which tubule
53. MEN2A pt. Most likely has high level of - calcitonin (Medullary thyroid ca)
57. Why capillaries has lowest flow? Surface area/distance from heart/
61. Pregnant lady rectal bleed stops after given birth. ?Cause - haemorrhoids
69. Father has colon ca age 53. Daughter also colon ca age 45. What genetic disease? Hnpcc/fap
70. Pt after horseriding/biking. Haematoma butterfly shape in perineal area not involving inguinal
canal. Which part of urethra involved -membranous urethra/bulbar urethra/prostetic urethra/penile
urethra
71. What growth factor cause angiogenesis? vascular endothelial growth factor (VEGF),
fibroblast growth factor (FGF), tumor necrosis factor-alpha (TNF-α), transforming growth
factor-beta (TGF-β), and the angiopoietins (Ang).
74. Nodules on elbow excised; hpe shows cholesterol. What is it? -xanthoma
75. Name of bacteria that invade and live in host to avoid phagocytosis.
78. Autosomal dominant disease pattern. What is the chance to get for the son if one parent has the
disease.
79. Meckels diverticulum origin- yolk stalk (the same name as vitello intestinal duct)