Blood flow throughout the periphery is regulated by
the autonomic nervous system
While in the hospital for management of acute lymphoid leukemia (ALL), a patient develops severe thrombocytopenia. The most appropriate action for this condition is
Activity restriction
Which type of leukemia primarily affects children?
ALL (Acute lymphoid leukemia)
A serious complication of deep vein thrombosis is
pulmonary embolus
Velocity of blood flow is measured in
Centimeters per second.
True or False: Seasonal allergic rhinitis is most involved in type II hypersensitivity reactions.
False
The principle Ig mediator of type I hypersensitivity reactions is
IgE.
Venous obstruction leads to edema because it ________ pressure.
increases capillary hydrostatic
The Philadelphia chromosome is a balanced chromosome translocation that forms a new gene called
bcr-abl.
When a patient is struck in the eye by a baseball, the result is redness and swelling. This increase in blood flow to a localized area is called
hyperemia.
The relationship of blood flow (Q), resistance (R), and pressure (P) in a vessel can be expressed by which equation?
Q = P/R
A 5-year-old patient’s parents report loss of appetite and fatigue in their child. The parents also state that the child refuses to walk as a result of pain. The child’s most likely diagnosis is
ALL (acute lymphoid leukemia)
What is the correct definition of complete remission (CR) of leukemia?
CR is less than 5% blasts in marrow and normal CBC values.
A primary effector cell of the type I hypersensitivity response is
mast cells.
The hypersensitivity reaction that does not involve antibody production is type
IV.
Myasthenia gravis is a type II hypersensitivity disorder that involves
impaired muscle function.
Patients with immunodeficiency disorders are usually first identified because they
develop recurrent infections
Which form of leukemia demonstrates the presence of the Philadelphia chromosome?
CML (chronic myeloid leukemia)
What laboratory finding is usually found in aplastic anemia?
Pancytopenia
TRUE/FALSE The anemia resulting from a deficiency of either vitamin B12 (cobalamin) or folate is caused by a disruption in DNA synthesis of the blast cells in the bone marrow that produces very large abnormal bone marrow cells called megaloblasts.
True
Pernicious anemia is caused by a lack of
intrinsic factor.
Excessive red cell lysis can be detected by measuring the serum
bilirubin.
Which vessel normally demonstrates the most rapid blood flow?
The vena cava
Red blood cells obtain nearly all their energy from metabolism of
glucose.
The conversion of plasminogen to plasmin results in
fibrinolysis.
The strength of the bond between oxygen and hemoglobin is known as the
oxygen-hemoglobin affinity
A patient is diagnosed with a tortuous blood vessel of the right hand that bleeds spontaneously. This patient presents with
telangiectasia.
What is necessary for red blood cell production?
Iron
The primary source of erythropoietin is provided by the
kidney.
Which causes vasoconstriction?
Norepinephrine
An increase in hemoglobin affinity for oxygen occurs with
shift to the left.
TRUE/FALSE Vaccination for pneumococcal pneumonia should be performed before 1 year of age in patients with sickle cell anemia.
False
Thalassemia may be confused with iron-deficiency anemia, because they are both
microcytic.
The final step in clot formation is
clot retraction.
A deficiency of von Willebrand factor impairs
platelet adhesion to injured tissue.
A low mean corpuscular hemoglobin concentration (MCHC) and mean corpuscular volume (MCV) are characteristic of which type of anemia?
Iron deficiency
The most appropriate treatment for secondary polycythemia is
measured to improve oxygenation
A child with a history of recent strep throat infection develops
glomerulonephritis. This is most likely a type
_____
hypersensitivity reaction.
III
group of clinical findings describes the typical presentation of ALL (acute lymphoid leukemia)?
Pain in long bones, infection, fever, bruising
In general, the best prognosis for long-term disease-free survival occurs with
ALL (acute lymphoid leukemia)
Certain autoimmune diseases are associated with the presence of
specific proteins on a person’s cells.
These proteins are called
________ proteins.
HLA or MHC
Autologous stem cell transplantation is a procedure in which
Stem cells are harvested from the patient and then returned to the same patient.
A 58-year-old woman is seen in the clinic for reports of severe back
pain. Her chest x-ray demonstrates
generalized bone
demineralization and compression fracture. Blood studies demonstrate
elevated calcium
levels. The most likely diagnosis is
myeloma
The effects of histamine release include
increased vascular permeability
Renal insufficiency is a common complication of which disease?
myeloma
A newborn has melena, bleeding from the umbilicus, and hematuria. The newborn most likely experiencing
vitamin K deficiency bleeding
A laboratory test finding helpful in confirming the diagnosis of iron-deficiency anemia is
elevated total iron-binding capacity
Dysfunction of which organ would lead to clotting factor deficiency?
Liver
The strength of the bond between oxygen and hemoglobin is known as the
oxygen-hemoglobin affinity
The most appropriate treatment for secondary polycythemia is
measure to improve oxygenation
When systemic vascular resistance is decreased, blood flow
decreases
A commonly ingested substance associated with prolongation of the bleeding time is
asprin
TRUE/FALSE Vaccination for pneumococcal pneumonia should be performed
before 1 year of age in patients with sickle
cell anemia.
False, Vaccination for pneumococcal pneumonia should be performed
before 2 years of age in patients with
sickle cell anemia and
booster vaccinations given 3 to 5 years later.
The prothrombin time (PT) and INR (international normalized ratio) measure the integrity of
extrinsic pathway
The megakaryocyte is a precursor to
platelets
The most effective therapy for anemia associated with kidney failure is
erythropoietin administration
Which condition is associated with an elevated reticulocyte count?
Hemolytic anemia
What are the two specific immune cells
T-cells & B-cells
What are the Non-Specific immune cells
Eosinophils, monocytes, macrophages, neutrophils, basophils.
What are the two types of alterations in the immune function
Excessive Immune response & Deficient immune response.
Excessive Immune response
Over-or hyper-functioning of immune system
Deficient Immune response
inefective imunne response
What is autoimmunity?
The immune system attacks its own tissues.
What appears to increase the risk of autoimmune disorders?
MHC gene (HLA)
females at higher risk
Hypersensitivity describes...
The mechanism of injury
True or False
Hypersensitivity and autoimmunity will eventually lead to inflammation.
True
Treatment for autoimmunity...
Individualized immunosuppressive therapy
1. Corticosteroids & Cytotoxins (MTX)
2. Tumor necrosis facto inhibitors
3. Therapeutic Plasmaphersis
Treatment for Type 1 hypersensitivity include:
IgE blocker therapy: Inhibits binding of IgE to mast cells; Antihistamines: Block the effects of histamine; Epinephrine: Counter effect of histamine (Epi Pen); Beta-adrenergic: decrease bronchoconstriction; Corticoidsteriods: Decrease inflammation response; Anticholinergics: Block parasympathetic system.
Malignant transformation of B-cell plasma cells
Plasma cell myeloma
Myeloid lineage or Lymphoid lineage?
B cells, T cells, and NK cells.
Lymphoid lineage
Myeloid lineage or Lymphoid lineage?
Red blood cells, platelets, monocytes, granulocytes.
Myeloid lineage
An example of neoplasms from the myeloid lineage include alterations in:
A. Granulocytes
B. B cells
C. T Cells
D. NKA cells
A. Granulocytes
Classification of hematologic neoplasms categories based on...
The cell type of the neoplasm
What are the three most common manifestations of Leukemia?
1. Anemia
2. Thrombocytopenia
3. Leukopenia (neutropenia)
Main typical symptoms of malignant disorders of white blood cells?
Recurrent infections and enlarged, non-tender lymph nodes.
Main treatments for malignant disorders of white blood cells...
Chemotherapy and Stem cell transplant
What type of leukemia:
-Adult
-Philadelphia chromosome (Ph+)
- bcr/abl
-High granulocyte count on the CBC
-does not respond well
to chemotherapy
CML (Chronic myeloid leukemia)
What type of leukemia:
-Abrupt onset
-Adults
-Poor prognosis
AML (Acute myeloid leukemia)
What type of leukemia:
-Most common, B cell precursors
-Bone Marrow infiltration: Reduces production of RBC/platlets
-Malignant lymphocytes invade lymphoid tissues and bone marrow-disrupt function
-asymptomatic, Usually found by accident in routine blood examination.
-5% associated with more aggressive T cells.
CLL (chronic lymphoid leukemia)
What type of leukemia:
-Primarily in children
-Better prognosis in children than adults
ALL (Acute lymphoid leukemia)
Hodgkins or Non-Hodgkin?
B cells/ EB virus/ 20-40ys male/ Contiguous lymphatic pathways/ Cervical nodes/ single node or localized node chain/ 85% 5 yr survival rate
Hodgkins
Hodgkins or Non-Hodgkin?
B, T and NK cells/ Burkitt lymphoma, Epstein Barr virus and HIV/ Older male/ Non-predicatable growth/ 50% 5-year survival rate
Non-Hosgkins
Associated with Reed-Sternberg cells, Hodgkins or Non Hodgkins?
Hodgkins
In Hodgkins, where is the most common site for lymph node enlargement?
Cervical nodes
In Non-Hodgkins what are two serious oncological emergencies that can occur
1. Superior vena cava obstruction
2. Spinal cord compression
-Most numerous
-4.2-6.2 million cells/mm3
-Buffer blood Ph-Carbonic anhydrase
Erythrocytes - RBC
Where is erythropoeitin (EPO) made?
Kidneys (only) in adults
newborns: LIver and kidneys
Nutritional requirements for erythropoiesis
requires adequate amounts of iron, protein, vitamins, and minerals
What is anemia?
Deficiency of red cells
What is polycythemia?
excess red cells
Absorption of B12 in the small intestine requires _______ _______, which is produced by the ______ ______ __ __ ________.
intrinsic factor
parietal cells of the stomach
Intestinal bacteria convert conjugated bilirubin into urobilinogen; execreted primarily in the stool but also in the urine is apart of what?
red cell destruction
What are the compensatory mechanisms to restore tissue oxygenation?
Increase HR, cardiac output, circulatory rate, and flow to vital organs. Increase in erythropoietin production/activity
SNS (sympathetic nervous system) activation:
Hypertension, HF, dyshythmia
Low oxygen-carying capacity leads to...
hypoxia
Stem cell disorder characterized by the reductio of hematopoietic tissue, fatty marrow replacement, and pancytopenia.
Aplastic anemia
Low RBC, WBC, and platelets
pancytopenia
How do you diagnosis aplastic anemia?
Diagnosed with bone marrow biopsy
Treatment for aplastic anemia
bone marrow transplantation
Failure of the renal endocrine function impairs erythropoietin production and bone marrow compensation.
Anemia of chronic renal failure.
Treatment for anemia of chronic renal failure
Diayalis, administration of erythropoietin, replacement of iron, folate and B12
Disruption in DNA synthesis of blast cells produces megaloblasts (macrocytic).
Anemia related to vitamin B12 (cobalamin) or folate deficiency
Due to lack of intrisic factors leading to vitamin B12 deficiency
Pernicious anemia
Clinical manifestations of pernicious anemia
Increase MCV, low RBC, WBC, and platelet count.
megaloblastic dysplasia.
Most common nutritional deficiency in the world.
Iron deficiency anemia.
In which anemia does serum ferritin level decrease
serum iron level decreased,
total iron binding capacity (TIBC) increased.
-microcytic
iron deficiency anemia
True or false;
Does iron deficiency cause Pica?
True
Treatment for iron deficiency anemia
Oral administration of ferrous sulfate or IV ferric gluconate (only in severe cases) Used for 4-6months
Increased RBC destruction (hemolysis) resulting in decreased RBC survival rates.
microcytic
Thalassemia
In Thalassemia,
associated with the mutant gene that suppresses the rate of globin chain synthesis
Autosomal recessive
term meaning: red blood cell size is smaller than the normal range
microcytic
Genetically determined defect of hemoglobin synthesis resulting in hemoglobin instability and insolubility.
Sickle cell anemia
Sickle cell anemia causes...
vascular occlusion
In what race is sickle cell almost exclusively in?
Black race
what cures sickle cell anemia
stem cell transplant
Maternal antibodies against Rh+ antigen on fetal RBC not inherited from mother causes...
from Rh incompatibility
Hemolytic disease of the newborn
What is the treatment for hemolytic disease of the newborn>
A standard dose of anti-RH immune globulin (RhoGAm) is given to the mother before or after delivery.
Initial response to a vascular injury involving the interaction between platelets and the endothelium of the injured vessel is....
the primary stage of hemostasis
Involves the formation of a fibrin clot through intrinsic and extrinsic pathways; coagulation
secondary stage of hemostasis
clot retraction
final stage of hemostasis
What is fibrinolysis?
Clot dissolution
When does fibrinolysis occur?
as fibrin clot is forming
What is the process of fibrinolysis?
Plasminogen activators
Plasmin digests fibrinogen and fibrin and inactivates factors V and VIII
What are critical for hemostasis?
Ca++ and Vit K
How do we evaluate primary and secondary hemostasis?
Laboratory test: CBC; Bleeding time: evaluates the vascular status and platelet function; PT/INR: assesses the extrinsic pathway of coagulation; aPTT assesses the intrinsic pathway.
In evaluating primary and secondary hemostasis, what does D-dimer reflect?
fibrinolysis
Caused by:Bone marrow suppression from chemotherapy; recent immunizations; alcohol ingestion
Thrombocytopenia
What is thrombocytopenia
Low platelet count. Prolonged bleeding time, petechiae, purpura.
What is the most common coagulation disorder?
Hemophilia
In laboratory test for the evaluation of primary and secondary hemostasis what foes PT/INR asses?
The extrinsic pathway of coagulation
What results from hemophilia?
excessive bleeding
Hemophilia is inherited by....
x linked recesisve (male dominant)
Hemophilia A is...
factor VII deficiency
Hemophilia B is...
(Christmas disease) factor IX deficiency
In hemophilia what is hallmark?
hemarthrosis
Autosomal dominant (equally make and female populaiton) caused by excessive bleeding.
Von Willebrand Disease
What are the causes of excessive bleeding in Von Willebrand Disease?
Prolonged bleeding time; prolonged aPTT
Normal platelet count, normal PT/INR
Acquired hemorrhagic syndrome in which clotting and bleeding occur simultaneouslt
(DIC) Disseminated Intravascular coagulation
Causes of DIC
trauma, malignancy, burns, shock and abruptio placentae
What happens to fibrinogen levels and platelet count in DIC
Decreases
Does bleeding time increase or decrease in DIC?
Increase
What happens to PT/INR/aPTT in DIC?
It is elevated
What happens to D-dimer/fibrin split products in DIC?
it is elevated
Treatment for DIC?
Fresh frozen plasma, packed RBC, platelets, or cryoprecipitate.
What is the treatment for hepatic disease?
Vitamin K administration and Platelet transfusion, fresh frozen plasma or whole/packed blood.
A stationary blood clot formed within a vessel or a chamber of the heart
Thrombus
Treatment for thrombus
anticoagulant therapy
thrombolytic drugs
surgery to remove thrombus
In a blood vessel obstruction, the arterial system obstruction manifests as...
distal ischemia
in a blood vessel obstruction, the venous system obstruction manifests as...
edema
An obstruction that results in reduced flow beyond the obstruction is....
downstream, ischemia
An obstruction that results in increased pressure before the obstruction
upstream, congestion
A traveling clot is a ....
embilus
An embolus leaving L ventricle is
Ischemia stroke
An embolus leaving R ventricle
pulmonary embolus
Hardening and narrowing in medium and large-sized arteries
Arteriosclerosis/atherosclerosis
In Arteriosclerosis/atherosclerosis
________ breach intimal layer; leukocytes and endothelial cells oxidize the lipids producing further damage.
Low-density lipoproteins
In Arteriosclerosis/atherosclerosis
Process______ to the arterial intima, initiating an inflammatory response and an increase in the vessel wall permeability.
initiated by endothelial surface damage.
In Arteriosclerosis/atherosclerosis
__________ normally confined to the other tunicas, drawn to the intima where they proliferate (hardening)
Media smooth muscle cells
In Arteriosclerosis/atherosclerosis
Excess lipid and debris accumulate within vessel wall and coalesce into lipid core.
Narrowing
In Arteriosclerosis/atherosclerosis, macrophages engulf the
lipids; foam cells
Arteriosclerosis/atherosclerosis, can lead to...
hypertension, cardiac and renal disease, peripheral arterial disease, stroke and myocardial infraction
what are nonmodifiable risk factors of Arteriosclerosis/atherosclerosis?
Age, gender, family history of CAD, ethnicity
what are modifiable risk factors of Arteriosclerosis/atherosclerosis?
physical activity, stress and mental health, tobacco usage, hypertension, cholesterol, obesity, glucose intolerance
Extreme vasoconstriction producing cessation of flow to fingers and toes.
Raynaud Syndrome
Localized arterial dilations, bulge otward
Aneurysms
Clinical manifestation of aneurysms
Aortic: sudden severe tearing pain, radiates into back/abdomen, shock
Classical signs of acute arterial occlusion (6P'S)
Pallor, paresthesia, paralysis, pain, polar, pulseless
Treatment for acute arterial occlusion
Medically and surgically