Model Test 8.6.13 and 9.6.13 Flashcards

(40 cards)

0
Q

MOP associations

A

Congenital malformation of hallux and over expression of BMP 4

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1
Q

Myosotis ossifficans progressiva

A

Involves all skeletal muscles except diaphragm and extra ocular

Smooth and cardiac muscles not involved

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2
Q

Splenic injury

A

1-sub capsular hematoma< 10% or non bleeding capsular laceration50% or intraparenchymal hematoma >2 cm or laceration > 3cm
4-ruptured intraparenchymal hematoma with bleed >25% devascularisation
5-avulsed spleen
4 and 5– splenectomy

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3
Q

Most common site of heterotopic ossification in MOP

A
  1. Neck
  2. spine
  3. shoulder girdle
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4
Q

Non absorbable suture materials

A
Silk
Polypropylene
Polyethylene
Cotton
Linen
Polyester
Polyamide
Nylon
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5
Q

Natural suture materials

A

Catgut
Silk
Cotton
Linen

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6
Q

Vertical gaze centre

A

Rostral interstitial nucleus of MLF and interstitial nucleus of cajal

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7
Q

Diseases transmitted by sandfly

A

Kala azar
Oriental sore
Oraya fever
Sandfly fever

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8
Q

Diseases transmitted by tsetse fly

A

Sleeping sickness

T.brusi

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9
Q

Diseases transmitted by louse

A

Pediculosis
Epidemic typhus
Relapsing fever
Trench fever

PERT

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10
Q

Chagas’ disease transmitted by

A

Reduvid bug

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11
Q

Diseases transmitted by rat flea

A

Bubonic plague
Endemic typhus
Chiggerosis
Hymenolepsis diminuta

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12
Q

Flexner wintesteiner rosettes

A

Retinoblastoma

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13
Q

Homer wright rosettes

A

Medulloblastoma

Neuroblastoma

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14
Q

Extended spectrum penicillins

A

Amino: ampicillin ,amoxicillin
Carboxy: carbenicillin,ticarcillin
Ureido: mezlocillin,azlocillin,piperacillin

Carboxy and ureidopenicillins : anti pseudomonal activity

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15
Q

Beta lactamase resistant penicillin

A
Oxacillin
Cloxacillin
Dicloxacillin
Nafcillin
Methicillin
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16
Q

Perivascular pseudo rosettes

A
Ependymoma
Medulloblastoma
PNET
Central neurocytoma
Glioblastoma
Pilomyxoid astrocytoma
17
Q

Lipoprotein lipase activators

A

Apo-c2 and apo c1

18
Q

Lipoprotein lipase inhibitors

A

Apo c3 and apo A2

19
Q

LCAT activator

20
Q

Systemic causes of hyperprolactinemia

A
Chronic renal failure
Hypothyroidism 
Cirrhosis 
Epilepsy
Pseudocyesis
21
Q

Drugs causing SIADH

A
Vincristine 
Vasopressin 
Oxytocin 
Nicotine 
CBZ
Chlorpropamide
Cyclophosphamide
Phenothiazine 
TCA
MAO inhibitors
SSRI
22
Q

Tx of choice for SIADH

A

Hypertonic saline
Water restriction

If unsuccessful DOC: demeclocycline

23
Q

Appearance of amyloid with Congo red on light microscopy

A

Pink or red colour to tissue deposits

24
Appearance of amyloid on light microscopy
Amorphous eosinophilic extra cellular substance
25
Appearance of amyloid with Congo red stain on polarising microscopy
Apple green birefringence
26
Appearance of amyloid on electron microscopy
Non branching fibrils of indefinite length | Diameter - 7.5 to 10 nm
27
Appearance of amyloid X-ray crystallography and infrared spectroscopy
Beta pleated sheet
28
Amyloid ANF deposition in
Isolated atrial amyloidosis | Misfolded prion protein disease
29
Amyloid alpha deposition in
Familial renal amyloidosis
30
Most common organ involved in secondary amyloidosis
Kidneys
31
Involvement of splenic follicles in amyloidosis
Sago spleen
32
Involvement of splenic sinuses and red pulp in amyloidosis
Lardaceous spleen
33
Most specific feature of AL amyloidosis
Macroglossia
34
Best site for biopsy in amyloidosis
Rectum
35
Specific site for biopsy in amyloidosis
Abdominal fat aspirate
36
Appearance of amyloid with iodine
Mahogany brown If sulfuric acid is added it turns violet
37
Infections affecting epididymis first
Gonorrhoea and tuberculosis
38
Infections affecting the testis first
Syphilis
39
Most sensitive screening test for SI carcinoid
Plasma level of chromogranin A