INactive hydatid cyst

Q According to WHO-IWGE ultrasonographic classification for Hydatid cyst, inactive cysts belong to which group
a) Group I
b)  Group 2
c) Group 3
d) Group 4

More question at www.mcqsurgery.com/hydatid

Answer: C

WHO Informal Working Group on Echinococcosis (WHO-IWGE) classification

Group 1: Active group – cysts larger than 2 cm and often fertile.
Group 2: Transition group – cysts starting to degenerate and entering a transitional stage because of host resistance or treatment, but may contain viable protoscolices.
Group 3: Inactive group – degenerated, partially or totally calcified cysts; unlikely to contain viable protoscolices.

Primary Hyperparathyroidism

Primary Hyperparathyroidism MCQ - Free Question
Q) Which is not a feature of primary hyperparathyroidism?
a) Increase Parathormone
b) Increase Calcium
c) Decreased phosphate
d) Dystrophic calcification
Answer – Free

Answer: d) Dystrophic calcification

Explanation: Clinical features of primary hyperparathyroidism include subperiosteal bone resorption, increased serum calcium, decreased phosphate levels, and elevated PTH. Dystrophic calcification is not typically seen in this condition.

Primary hyperparathyroidism is most commonly caused by parathyroid adenoma (75%) and can be localized using sestamibi scan. Kidney stones are the most frequent symptomatic manifestation. It is defined by hypercalcemia with inappropriately normal or elevated PTH.

Associated disorders: peptic ulcers, pancreatitis, bone disease, and CNS symptoms.

Indications for surgery in asymptomatic patients include:

  • Age < 50 years
  • High urinary calcium excretion
  • Low creatinine clearance
  • Kidney stones
  • Very high serum calcium

Reference: Bailey and Love, 27th Edition, Page 826

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Paraneoplastic syndrome in HCC

Q) Paraneoplastic Syndrome in HCC which also occurs in End stage liver disease ?

a) Hypercholesteremia

b) Hypoglycemia

c) Hypercalcemia

d) Carcinoid

Ans -  b

Hypoglycemia (also seen in end stage liver disease) 

Erythrocytosis

Hypercalcemia

Dysfibrogenimea

Carcinoid Syndrome

Thyroxin binding globulinincreases

Porphyria cutanea tarda

Gynecomastia, testicular atrophy, early puberty

Timing of cholecystectomy in biliary pancreatitis

Q) What is true regarding timing of cholecystectomy in biliary pancreatitis ?

a) Cholecystectomy should be done before discharge in severe pancreatitis to prevent recurrent attacks

b) Cholecystectomy should be done in same admission as pancreatitis when severe disease is excluded

c) Early cholecystectomy has been shown to have more complications than interval cholecystectomy

d) Early cholecystectomy increases technical complications

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Questions on Bile ducts?

 Ans b

"Poncho trial " answers this question of timing of cholecystectomy in biliary pancreatitis 

Early cholecystectomy (just before discharge, when the patient has recovered and severe disease excluded), compared to interval cholecystectomy, effectively reduces---

  1. The rate of recurrent gallstone-related complications in patients with mild biliary pancreatitis,
  2. low added risk of complications.

Evidence on the timing of cholecystectomy in severe pancreatitis is scarce. Cholecystectomy is recommended after all signs of pancreatic necrosis have been resolved or if they persist more than 6 weeks

  • Cholecystectomy during the same admission is recommended for patients with mild biliary pancreatitis to prevent recurrent attacks.
  • In cases of severe pancreatitis, surgery is generally delayed until the inflammation subsides.
  • Studies have shown that early cholecystectomy during the same admission for mild to moderate biliary pancreatitis does not increase complications compared to delayed or interval cholecystectomy.

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Skin grafting

Q) In preop evaluation before placing skin graft over wounded area…bacterial colony count must be less than

a) 10000
b) 100000
c) 1000000
d) 10000000

ans b)  10 raise to the power 5

In advanced surgical practice, the bacterial colony count is a critical factor when considering the placement of a skin graft over a wounded area. The threshold for bacterial contamination in the wound is typically 100,000 colony-forming units (CFU) per gram of tissue. If the bacterial count exceeds this limit, the risk of postoperative infection, graft failure, and delayed healing increases significantly.

This threshold is based on several key factors:

  • Wound infection: A bacterial count above 100,000 CFU per gram is associated with a high risk of wound infection, which can lead to graft failure.
  • Graft survival: A sterile or minimally contaminated wound is crucial for graft take. Any significant bacterial load can compromise the graft's survival due to the impaired healing environment.

Prerequisites for skin grafting:
The recipient site should be assessed for potential bacterial load, blood supply,
presence of devitalized tissue, and exposed vital structures.
Donor site availability
Perform recipient site tissue culture if history or concern for infection (counts <100000
CFU/g tissue for most pathogens required before grafting).

Presence of group a beta heamolytic streptococci is absolute contraindication for skin grafting
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Skin grafting cultures