In a woman who presents in her first trimester of her first pregnancy with a platelet count of 80 F1F1F1S1F1F1F10 109/L, you must consider which of the following diagnoses?

A) Gestational thrombocytopenia B) ITP C) Eclampsia [HELLP syndrome (hemolytic anemias, elevated liver enzymes, and low platelet count)] D) Folic acid deficiency E) All of the above A) Gestational thrombocytopenia B) ITP C) Eclampsia [HELLP syndrome (hemolytic anemias, elevated liver enzymes, and low platelet count)] D) Folic acid deficiency E) All of the above

Exam 25: Disorders of Primary Hemostasis: Quantitative and Qualitative Platelet Disorders and Vascular Disorders

Laboratory findings in the storage pool deficiencies include all of the following except:

(Multiple Choice)

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Question 21

Which laboratory findings differentiate vWD from Glanzmann's thrombasthenia?

(Multiple Choice)

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Question 22

Glanzmann's thrombasthenia and congenital afibrinogenemia are qualitative disorders of platelet __________.

(Multiple Choice)

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Question 23

A patient whose serum contains or is known to have contained the antibody to the P1^A¹ antigen should receive __________ in all subsequent transfusions.

(Multiple Choice)

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Question 24

All of the following are possible mechanisms for the pathogenesis in TTP except:

(Multiple Choice)

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Question 25

The treatment of choice for chronic ITP after failure to maintain an adequate response to steroid therapy is _________.

(Multiple Choice)

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Question 26

Treatment of patients with Glanzmann's thrombasthenia who present with severe bleeding episodes is __________.

(Multiple Choice)

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Question 27

__________ is an immune disorder that presents with thrombocytopenia one week after transfusion of blood or blood products containing platelets.

(Multiple Choice)

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Question 28

Thrombocytosis may result from which of the following?

(Multiple Choice)

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Question 29

Quantitative congenital disorders that produce hypoplasia of megakaryocytes include all of the following except:

(Multiple Choice)

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Question 30

A qualitative disorder of platelet secretion is __________.

(Multiple Choice)

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Question 31

The most common clinical and diagnostic finding of vascular disorders is _____________.

(Multiple Choice)

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Question 32

Which laboratory findings differentiate Bernard-Soulier syndrome from Glanzmann's thrombasthenia?

(Multiple Choice)

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Question 33

Which strongly immunogenic antigen is associated with isoimmune neonatal thrombocytopenia?

(Multiple Choice)

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Question 34

In a woman who presents in her first trimester of her first pregnancy with a platelet count of 80  10⁹/L, you must consider which of the following diagnoses?

(Multiple Choice)

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Question 35

__________ is a frequently observed complication of heparin therapy.

(Multiple Choice)

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Question 36

The treatment of choice for patients diagnosed with TTP is __________.

(Multiple Choice)

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Question 37

The __________ is used to detect quantitative platelet disorders.

(Multiple Choice)

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Question 38

Laboratory findings that are hallmarks of Glanzmann's thrombasthenia include all but which of the following?

(Multiple Choice)

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Question 39

The platelet count is a routine screening test used to detect __________ changes such as thrombocytosis and thrombocytopenia.

(Multiple Choice)

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Question 40

Showing 21 - 40 of 62

Exam 25: Disorders of Primary Hemostasis: Quantitative and Qualitative Platelet Disorders and Vascular Disorders

Laboratory findings in the storage pool deficiencies include all of the following except:

Which laboratory findings differentiate vWD from Glanzmann's thrombasthenia?

Glanzmann's thrombasthenia and congenital afibrinogenemia are qualitative disorders of platelet __________.

A patient whose serum contains or is known to have contained the antibody to the P1A¹ antigen should receive __________ in all subsequent transfusions.

All of the following are possible mechanisms for the pathogenesis in TTP except:

The treatment of choice for chronic ITP after failure to maintain an adequate response to steroid therapy is _________.

Treatment of patients with Glanzmann's thrombasthenia who present with severe bleeding episodes is __________.

__________ is an immune disorder that presents with thrombocytopenia one week after transfusion of blood or blood products containing platelets.

Thrombocytosis may result from which of the following?

Quantitative congenital disorders that produce hypoplasia of megakaryocytes include all of the following except:

A qualitative disorder of platelet secretion is __________.

The most common clinical and diagnostic finding of vascular disorders is _____________.

Which laboratory findings differentiate Bernard-Soulier syndrome from Glanzmann's thrombasthenia?

Which strongly immunogenic antigen is associated with isoimmune neonatal thrombocytopenia?

In a woman who presents in her first trimester of her first pregnancy with a platelet count of 80  109/L, you must consider which of the following diagnoses?

__________ is a frequently observed complication of heparin therapy.

The treatment of choice for patients diagnosed with TTP is __________.

The __________ is used to detect quantitative platelet disorders.

Laboratory findings that are hallmarks of Glanzmann's thrombasthenia include all but which of the following?

The platelet count is a routine screening test used to detect __________ changes such as thrombocytosis and thrombocytopenia.

Morphology of Human Blood and Marrow Cells: Hematopoiesis

Bone Marrow

The Red Blood Cell: Structure and Function

Anemia: Diagnosis and Clinical Considerations

Evaluation of Red Blood Cell Morphology and Introduction to Platelet and White Blood Cell Morphology

Iron Metabolism and Hypochromic Anemias

Megaloblastic Anemias

Aplastic Anemia Including Pure Red Cell Aplasia and Congenital Dyserythropoietic Anemia and Paroxysmal Nocturnal Hemoglobinuria

Introduction to Hemolytic Anemias: Intracorpuscular Defects: I Hereditary Defects of the Red Cell Membrane

Hemolytic Anemias: Intracorpuscular Defects: II Hereditary Enzyme Deficiencies

Hemolytic Anemias: Intracorpuscular Defects: III the Hemoglobinopathies

Hemolytic Anemias: Intracorpuscular Defects: Iv Thalassemia

Hemolytic Anemias: Extracorpuscular Defects

Hypoproliferative Anemia: Anemia Associated With Systemic Diseases

Cell Biology, Disorders of Neutrophils, Infectious Mononucleosis, and Reactive Lymphocytosis

Introduction to Leukemia and the Acute Leukemias

Chronic Myeloproliferative Disorders I: Chronic Myelogenous Leukemia

Chronic Myeloproliferative Disorders Ii: Polycythemia Vera, Essential Thrombocythemia, and Idiopathic Myelofibrosis

Myelodysplastic Syndromes

Chronic Lymphocytic Leukemia and Related Lymphoproliferative Disorders

The Lymphomas

Multiple Myeloma and Related Plasma Cell Disorders

Lipid Lysosomal Storage Diseases and Histiocytosis

Introduction to Hemostasis

Disorders of Plasma Clotting Factors

Interaction of the Fibrinolytic, Coagulation, and Kinin Systems; Disseminated Intravascular Coagulation; and Related Pathology

Introduction to Thrombosis and Anticoagulant Therapy

Quality Control in the Hematology Laboratory

Body Fluid Examination: the Qualitative, Quantitative, and Morphologic Analysis of Serous, Cerebrospinal, and Synovial Fluids

Hematology Methods

Principles of Automated Differential Analysis

Coagulation Procedures

Applications of Flow Cytometry to Hematology and Hemostasis

Molecular Diagnostic Techniques in Hematopathology

Special Stainscytochemistry

Filters

A patient whose serum contains or is known to have contained the antibody to the P1^A¹ antigen should receive __________ in all subsequent transfusions.

In a woman who presents in her first trimester of her first pregnancy with a platelet count of 80  10⁹/L, you must consider which of the following diagnoses?