A. Malignant melanoma
B. Squamous cell carcinoma
C. Kaposi’s sarcoma
D. Ewing’s sarcoma
Related Mcqs:
- A 3-year old child presented with progressive anaemia, jaundice & failure to thrive. O/E: pallor, splenomegaly are seen Peripheral smear showed normoblasts and small round intensely stained red cells. The likely diagnosis is________________?
A. Here ditary spherocytosis
B. Thalassaemia
C. Sickle cell anaemia
D. Vitamin B12 deficiency anaemia - A child’s CSF was examined I contains slightly raised or normal PMN cells, raised lymphocytes, absence of mycotic growth, value of protein is normal or above normal, glucose level is normal. The most probable diagnosis is____________?
A. Pyogenic bacterial meningitis
B. Viral meningitis
C. Fungal meningitis
D. Tuberculous meningitis - Frozen sections can be used for the demonstration of_____________?
A. Fat
B. Mucin
C. Cartilage
D. Iron - Stain used for demonstration of amyloid is______________?
A. Congo Red
B. Masson’s toichrome
C. Vonkosa
D. Reticulin - Muscle glycogen, which cannot contribute to blood glucose due to the absence of which enzymes ?
A. Phosphoglutamase
B. Branching enzyme
C. Debranching enzyme
D. Glucose-6-phosphotase - Muscle glycogen cannot contribute directly to blood glucose level because___________?
A. Muscle lacks glucose 6 phosphatase
B. Muscle lacks phospho gluco isomerase
C. Absence of glucokinase
D. Muscle does not contain glycogen phosphorylase - Glycogen synthesis is increased by_____________?
A. Cortisone
B. Insulin
C. GH
D. Epinephrine - In which type of glycogen storage disease is hyper uricemia a feature ?
A. I
B. II
C. III
D. IV - Glycogen breakdown leads to formation of______________?
A. Glucose
B. Lactic acid
C. Glucose & Lactic acid
D. Glycoprotein - Type II glycogen storage disorder is due to deficiency of______________?
A. Alpha -Glucosidase
B. Alpha galactosidase
C. Muscle phosphorylase
D. Acid Lipase
