Order Diseases of the Blood Discussion

Order Diseases of the Blood Discussion
Order Diseases of the Blood Discussion
. A patient with chronic myelogenous leukemia who developsleft upper quadrant pain radiating to the left shoulder probably has
A. splenic infarction
B. perforated gastric ulcer C. pancreatitis D. ischemic colitis E. renal stone
566. The highest titers of heterophil reactions
172 / Diseases of the Blood
568. Acute myeloblastic leukemia (AML) is characterized by
A. peak incidence in childhood
B. high leukocyte alkaline phosphatase
C. Philadelphia chromosome
D. Auer bodies in blast cells E. response to vincristine and prednisone
569. Red urine may be caused by all of the following EXCEPTA. urobilinuria
B. hemoglobinuria
C. porphyrinuria D. myoglobinuria
E. presence of red corpuscles
570. All of the following are generally associated with secondary
polycythemia EXCEPT
A. Cushing’s syndrome
B. uterine myomata
C. hypernephroma
D. gastric malignancy
E. cerebellar hemangiomas
571. Elevation of the serum acid phosphatase is seen in A. Hodgkin’s disease
B. multiple myeloma
C. Gaucher’s disease D. Niemann-Pick disease
E. acute leukemia
572. All of the following hemoglobins migrate slower on paper
electrophoresis than type A hemoglobin EXCEPT
A. S
B. C
C. D
D. Barts
E. A:
Order Diseases of the Blood Discussion
573. Infectious mononucleosis is characterized by all of the following EXCEPT
A. antibodies to EB virus B. heterophil antibodies C. antinuclear antibodies D. anti-I antibodies
E. antibodies to sheep red cells
Diseases of the Blood / 173574. Normal hemoglobin molecules are composed of
A. two alpha and two beta chains
B. one alpha and one beta chain
C. four alpha chains D. four beta chains
E. two alpha and two delta chains
575. In chronic granulomatous disease of childhood, infectionsresult from
A. low complement levels B. defective bacterial killing by neutrophils C. defective bacterial ingestion by neutrophils D. neutropenia
E. lymphopenia
576. Bleeding from von Willebrand’s disease is best treated withA. platelet infusion
B. cryoprecipitate C. stored plasma
D. prothrombin complex
E. whole blood
577. All of the following purpuras have thrombocytopenia EX-CEPT
A. idiopathic thrombocytopenia purpura
B. disseminated lupus erythematosus
C. infectious purpura (e.g., rubeola, varicella) D. acute leukemia
E. Henoch-Schonlein purpura
578. Quick prothrombin time is prolonged in all of the followingconditions EXCEPT
A. fibrinogen deficiency
B. vitamin K deficiency C. Factor V deficiency D. hemophilia (AHG deficiency)
E. Factor VII deficiency
579. Hemophilia A can be characterized by A. normal immunoreactive Factor VIII
B. normal functional Factor VIII
C. decreased immunoreactive Factor VIII
I), prolonged bleeding time
E. platelet function abnormality
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