Neurosurgery Practice QnA 2nd Part Flashcards
(255 cards)
Relative contraindications for surgery for spinal metastasis include all of the following EXCEPT:
A. Multiple myeloma
B. Recurrence after maximal radiation
C. Multiple lesions at multiple levels
D. Total paralysis for > 48 hours
E. Expected survival < 3 monthsB. Recurrence after maximal radiation
Recurrence after maximal radiation is an indication to operate.
Which of the following is the usual radiation dose for spinal epidural metastasis?
A. 20 Gy in 2 Gy fractions over 10 days
B. 30 Gy in 3 Gy fractions over 10 days
C. 60 Gy in 6 Gy fractions over 10 days
D. 100 Gy in 10 Gy fractions over 10 days
E. 200 Gy in 50 Gy fractions over 30 days
There is a predilection to sensory and motor nerves of the limbs and ciliary muscle/nerve.
Match the following toxins with the appropriate fi ndings:
A. Tetanus
B. Botulism
C. Diphtheria
D. Reye’s syndrome
Diphtheria toxin has a predilection to sensory and motor nerves of the limbs
and ciliary muscles or nerves.
It typically presents with risus sardonicus.
Match the following toxins with the appropriate findings:
A. Tetanus
B. Botulism
C. Diphtheria
D. Reye’s syndrome
Tetanus may typically present with trismus, risus sardonicus, tonic spasms,
and generalized convulsions.
The initial symptom is usually diffi culty in convergence of the eyes.
Match the following toxins with the appropriate fi ndings:
A. Tetanus
B. Botulism
C. Diphtheria
D. Reye’s syndrome
Symptoms appear 12–48 hours after ingestion and may be preceded by nausea, vomiting, and diarrhea. The convergence diffi culty is usually followed by
ptosis and extraocular muscle paralysis
Encephalopathy typically develops 4 to 7 days after the onset of the illness
Match the following toxins with the appropriate fi ndings:
A. Tetanus
B. Botulism
C. Diphtheria
D. Reye’s syndrome
This is a typical feature of Reye’s syndrome
Which statement is true regarding the presentation of multiple myeloma in the spine?
A. Hypocalcemia occurs in 25% of patients.
B. Bone pain is characteristically at rest and with movement.
C. There is occurrence of amyloidosis.
D. Invasion of the spinal canal occurs in over 50% of patients.
E. Defi nitive diagnosis can be made by plain X-ray.
Patients with spinal multiple myeloma typically present with hypercalcemia,
bone pain characteristically absent at rest, and spinal canal invasion in about
10% of cases. Multiple myeloma (MM) and amyloid light-chain (AL) amyloidosis are caused by the expansion of monoclonal plasma cells and secretion
of dysproteinemia (Bence Jones protein and free light chain).
Criteria for the diagnosis of multiple myeloma include all of the following EXCEPT:
A. Biopsy-proven plasmacytoma
B. Myeloma cells in a single peripheral blood smear
C. Plasma cells > 10 of 1000 cells on marrow morphology
D. Radiographic survey demonstrating lytic lesions
E. Monoclonal immunoglobulins in the urine or blood
Myeloma cells in two or more peripheral blood smears are required.
The Batson plexus route of spinal metastases spread represents which type of spread?
A. Perinervous
B. Arterial
C. Venous
D. Direct extension
E. All of the above
It represents spread via spinal epidural veins. The Batson venous plexus is a
network of valveless veins in the human body that connect the deep pelvic
veins and thoracic veins to the internal vertebral venous plexuses.
Facioscapulohumeral dystrophy (Landouzy–Dejerine’s syndrome)
Match the following chromosomal abnormality with the appropriate disease or
syndrome:
A. 5q
B. 5p
C. 4
D. 9
E. None of the above
Facioscapulohumoral dystrophy, or Landouzy-Dejerine’s syndrome is associated with a defect on chromosome 4.
Match the following chromosomal abnormality with the appropriate disease or
syndrome:
A. 5q
B. 5p
C. 4
D. 9
E. None of the above
Werdnig-Hoff mann’s disease has autosomal recessive inheritance on chromosome 5q.
Myotonic muscular dystrophy
Match the following chromosomal abnormality with the appropriate disease or
syndrome:
A. 5q
B. 5p
C. 4
D. 9
E. None of the above
Myotonic muscular dystrophy has autosomal dominant inheritance on chromosome 19.
Cri du chat syndrome
Match the following chromosomal abnormality with the appropriate disease or
syndrome:
A. 5q
B. 5p
C. 4
D. 9
E. None of the above
Cri du chat syndrome is due to a 5p deletion and results in microcephaly,
hypertelorism, and congenital heart disease.
Friedreich’s ataxia
Match the following chromosomal abnormality with the appropriate disease or
syndrome:
A. 5q
B. 5p
C. 4
D. 9
E. None of the above
Friedreich’s ataxia has autosomal recessive inheritance on chromosome 9. It
is named after German pathologist and neurologist Nikolaus Friedreich who
identifi ed this disease in 1863.
Preferred agent for patients with systolic heart failure
Match the antiarrhythmic with the appropriate statement:
A. Verapamil
B. Diltiazem
C. Digoxin
D. Procainamide
E. Esmolol
Diltiazem is the preferred agent for patients with systolic heart failure because it produces less myocardial depression than verapamil.
Side effects of hypotension and negative inotropic effect
Match the antiarrhythmic with the appropriate statement:
A. Verapamil
B. Diltiazem
C. Digoxin
D. Procainamide
E. Esmolol
Verapamil’s side eff ects include hypotension and worsening of systolic heart
failure due to negative inotropic eff ect.
Indicated for chronic rate control of atrial fi brillation
Match the antiarrhythmic with the appropriate statement:
A. Verapamil
B. Diltiazem
C. Digoxin
D. Procainamide
E. Esmolol
Digoxin is indicated for chronic rate control of atrial fi brillation. Because of
its delayed action it is not indicated in acute atrial fi brillation.
Contraindicated in patients with prolonged QT interval
Match the antiarrhythmic with the appropriate statement:
A. Verapamil
B. Diltiazem
C. Digoxin
D. Procainamide
E. Esmolol
Procainamide is contraindicated in patients with prolonged QT interval because it prolongs QT interval and may be pro-arrhythmic. It is used to convert atrial fi brillation to normal sinus rhythm.
Indicated for rate control of atrial fi brillation in the setting of a hyperadrenergic state
Match the antiarrhythmic with the appropriate statement:
A. Verapamil
B. Diltiazem
C. Digoxin
D. Procainamide
E. Esmolol
Beta-blockers are indicated for rate control of atrial fi brillation in the setting
of a hyperadrenergic state such as acute myocardial infarction after bypass
surgery
A 56-year-old woman just had a large frontal tumor resected that stained positive for reticulin on immunostaining. The tumor histology contained mitotic fi gures as well as necrosis and pseudopalisading. The most likely diagnosis is
A. ganglioglioma.
B. gliosarcoma.
C. glioblastoma multiforme.
D. gliomatosis cerebri.
E. germinoma.
A. ganglioglioma.
B. gliosarcoma.
C. glioblastoma multiforme.
D. gliomatosis cerebri.
E. germinoma.
Gliosarcoma has the same histological features as glioblastoma multiforme.
In addition, it does stain for reticulin in the sarcomatous part of the tumor.
Approximately 2% of glioblastomas are gliosarcomas
Which of the following is true regarding management of the blunt injury shown here?
A. Those with mild neurological defi cits and accessible lesions are better managed by repair than ligation.
B. Proximal occlusion may be accomplished by an anterior approach with mobilization of the sternocleidomastoid.
C. Endovascular embolization with detachable balloons may be used for management.
D. All of the above are true.
E. None of the above are true.
Blunt trauma injuries to the cervical vertebral artery are more often managed by ligation than repair. Ligation may be risky since only ~ 20% of the
general population has a complete collateral circulation. Proximal occlusion
may be accomplished by an anterior approach with mobilization of the sternocleidomastoid. Endovascular treatment with detachable balloons is a valid
option for management.
Peripheral neuropathy, malaise, nausea, and vomiting
Match the following metals with the corresponding syndrome:
A. Mercury
B. Manganese
C. Arsenic
D. Aluminum
E. Lead
Arsenic causes peripheral neuropathy, nausea, and vomiting.
Encephalitis in children
Match the following metals with the corresponding syndrome:
A. Mercury
B. Manganese
C. Arsenic
D. Aluminum
E. Lead
Lead causes encephalitis in children as well as pica, irritability, seizures, abdominal cramping, ataxia, coma, and high intracranial pressure.
Rigidity, bradykinesia
Match the following metals with the corresponding syndrome:
A. Mercury
B. Manganese
C. Arsenic
D. Aluminum
E. Lead
Manganese causes a Parkinson-like syndrome.