Chapter 3 Hematopoietic Flashcards

1
Q

Key players in the inflammatory response and in fighting infections
Normal range

A

Leukocytes

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2
Q

One type of leukocytes

Usually the first to arrive at the site of infection

A

Neutrophils

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3
Q

Kissing disease-oral transmission
Self-limiting
Most prevalent in adolescents and young adults
Caused by Epstein-Barr virus in the herpes family

A

Mononucleosis

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4
Q

Least common of the 2
Solid tumors with the presence of Reed-Sternberg cells
Typically originate in the lymph nodes of the upper body
Curable with treatment
Painless enlarged nodes, weight loss, fever, night sweats, purity’s, coughing, difficulty breathing, chest pain, recurrent infections, and splenomegaly

A

Hodgkin’s lymphoma

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5
Q

More common
Poor prognosis
Can originate in the T or B cells
No Reed-Sternberg cells

A

Non hodgkins lymphoma

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6
Q

Second most common blood cancer

Cancer of the leukocytes

A

Leukemia

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7
Q

Affects primarily children
Responds well to therapy
Good prognosis
Type of leukemia

A

Acute lymphoblastic leukemia

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8
Q

Affects primarily adults
Responds fairly well to treatment
Prognosis somewhat worse than that of the acute
Type of leukemia

A

Acute myeloid leukemia

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9
Q

Affects primarily adults
Responds poorly to therapy, yet most patients live many years after diagnosis
Type of leukemia

A

Chronic lymphoid leukemia

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10
Q

Affects primarily adults

Responds poorly to chemo, but the prognosis is improved with allogenic bone marrow transplant

A

Chronic myeloid leukemia

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11
Q

Plasma cell cancer
Excessive numbers of abnormal plasma cells in the bone marrow, crowding the blood forming cells and causing Bence Jone proteins to be excreted in the urine
Bone destruction leads to hypercalcemia and pathological fractures

A

Multiple myeloma

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12
Q

Results from a decreased number of erythrocytes, reduction of hemoglobin, or presence of abnormal hemoglobin
Decreases o2 carrying capacity leading to tissue hypoxia

A

Anemia

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13
Q

Very common

Iron is necessary for hemoglobin production

A

Iron-deficiency anemia

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14
Q

Vitamin b12 deficiency usually caused by a lack of intrinsic factor
Autoimmune
Vitamin b12 required for dna synthesis
Leads to decreased maturation and cell division
May see myelin breakdown and neurological complications

A

Pernicious anemia

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15
Q

Bone marrow depression of all blood cells (pancytopenia)

A

Aplastic anemia

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16
Q

Excessive erythrocyte destruction

Blood

A

Hemolytic anemia

17
Q

Neither recessive nor dominant-co-dominant

Hemoglobin s causes erythrocytes to be abnormally shaped

A

Sickle cell anemia

18
Q

Autosomal dominant inheritance

Abnormal hemoglobin from a lack of one of two proteins that make up hemoglobin

A

Thalassemia

19
Q

Abnormally high erythrocytes
Rare
Considered neoplastic disease
Increased blood volume and viscosity, leading to tissue ischemia and necrosis

A

Polycythemia

20
Q

X-linked recessive bleeding disorder

Deficiency or abnormality of clotting factor VIII

A

Hemophilia A

21
Q

Most common hereditary bleeding disorder

Decreased platelet adhesion and aggregation

A

Von Willebrand’s disease

22
Q

Life-threatening complication of many conditions
Inappropriate immune response
Widespread coagulation followed by massive bleeding because of the depletion of clotting factors

A

Disseminated intravascular coagulation

23
Q

HYPOcoagulation resulting from an autoimmune destruction of platelets

A

Idiopathic thrombocytopenia purpura

24
Q

Deficiency of enzyme necessary for cleaving von willebrand’s factor, leading to hyper coagulation
Hypercoagulation depletes platelet levels

A

Thrombotic Thrombocytopenic Purpura