Hematology Flashcards

study (51 cards)

1
Q

What is the composition of blood?

A

Blood is composed of formed elements and plasma, with approximate percentages:
* Red Blood Cells (RBCs): ~45%
* Plasma: ~55%
* White Blood Cells (WBCs) & Platelets: ~1%

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2
Q

What are the main components of plasma?

A

Plasma is composed of:
* Water: ~92%
* Proteins: ~7%
* Albumin: ~60% of plasma proteins
* Globulins
* Fibrinogen
* Other Components: ~1%

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3
Q

What is hematopoiesis?

A

Hematopoiesis is the process of blood cell formation in the bone marrow.

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4
Q

What are myeloid stem cells responsible for?

A

Myeloid stem cells give rise to:
* Erythrocytes (RBCs)
* Leukocytes (WBCs)
* Platelets

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5
Q

What are lymphoid stem cells responsible for?

A

Lymphoid stem cells give rise to:
* T Lymphocytes
* B Lymphocytes
* Natural Killers (NK cells)

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6
Q

What are histiocytes?

A

Histiocytes are immune cells originating from monocytes, working within tissues to defend the body.

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7
Q

What is the average lifespan of red blood cells (RBCs)?

A

The average lifespan of RBCs is 120 days.

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8
Q

What do neutrophils do?

A

Neutrophils fight bacterial infections via phagocytosis.

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9
Q

What is thrombopoietin?

A

Thrombopoietin is a hormone that regulates platelet production in the marrow.

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10
Q

What are the causes of anemia?

A

Causes of anemia include:
* Severe blood loss
* Inadequate RBC production
* Increased RBC destruction
* Deficiency of necessary components

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11
Q

What characterizes Sickle Cell Disease?

A

Sickle Cell Disease is an autosomal recessive disorder caused by the HbS gene, leading to abnormal hemoglobin and sickle-shaped RBCs.

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12
Q

What are the types of Sickle Cell Crisis?

A

Types of Sickle Cell Crisis include:
* Acute Vaso-Occlusive Crisis
* Aplastic Crisis
* Sequestration Crisis

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13
Q

What are common symptoms of febrile non-hemolytic transfusion reactions?

A

Symptoms include fever, chills, and headache.

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14
Q

What is thrombocytopenia?

A

Thrombocytopenia is a low platelet count caused by decreased production, increased destruction, or increased consumption of platelets.

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15
Q

What is disseminated intravascular coagulation (DIC)?

A

DIC is a life-threatening condition where clotting and anti-clotting occur simultaneously, indicating an underlying disorder.

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16
Q

What is hemophilia?

A

Hemophilia is an inherited bleeding disorder due to a deficiency in either factor VIII or factor IX.

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17
Q

What is neutropenia?

A

Neutropenia is a decrease in neutrophils (less than 2000/mm³), increasing the risk for infection.

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18
Q

What are the types of leukemia?

A

Types of leukemia include:
* Acute myeloid leukemia (AML)
* Chronic myeloid leukemia (CML)
* Acute lymphocytic leukemia (ALL)
* Chronic lymphocytic leukemia (CLL)

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19
Q

What is the most common manifestation of acute myeloid leukemia (AML)?

A

Manifestations include fever, infection, weakness, fatigue, and bleeding tendencies.

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20
Q

What is the average lifespan of platelets?

A

The average lifespan of platelets is 10 days.

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21
Q

What is the role of albumin in plasma?

A

Albumin maintains osmotic pressure and transports molecules.

22
Q

Fill in the blank: The average lifespan of a platelet is ______.

23
Q

True or False: Erythropoiesis is the process of making white blood cells.

24
Q

What is the primary function of lymphocytes?

A

Lymphocytes are an integral component of the immune system.

25
What is Acute Myeloid Leukemia (AML)?
A type of blood cancer characterized by the rapid growth of abnormal myeloid cells.
26
What are the common symptoms of AML?
* Fatigue * Weakness * Fever * Weight loss * Night sweats * Bone pain
27
What is the treatment for Acute Myeloid Leukemia (AML)?
* Aggressive chemotherapy—induction therapy * Hematopoietic stem cell transplantation * Supportive care * Antimicrobial therapy and transfusions
28
What happens if Acute Myeloid Leukemia (AML) is untreated?
Death occurs within months.
29
What is Chronic Myeloid Leukemia (CML)?
A blood cancer caused by a mutation in the myeloid stem cell, leading to uncontrolled production of immature white blood cells.
30
What are the clinical phases of Chronic Myeloid Leukemia (CML)?
* Chronic Phase * Accelerated Phase * Blast Crisis
31
What are the symptoms during the Blast Crisis of CML?
* Very high WBCs * Dyspnea * Confusion * Fever * Bone pain * Weight loss
32
How does Acute Lymphocytic Leukemia (ALL) differ from other leukemias?
It involves uncontrolled growth of immature cells from lymphoid stem cells and is most common in young children.
33
What is the peak age for Acute Lymphocytic Leukemia (ALL)?
4 years old.
34
What are the common manifestations of Acute Lymphocytic Leukemia (ALL)?
* Pain from enlarged liver/spleen * Bone pain * CNS symptoms * Headache * Vomiting
35
What is the treatment for Acute Lymphocytic Leukemia (ALL)?
* Chemotherapy * Monoclonal antibody therapy * Corticosteroids
36
What characterizes Chronic Lymphocytic Leukemia (CLL)?
It is the most prevalent type of adult leukemia, derived from a malignant clone of B lymphocytes.
37
What are the manifestations of Chronic Lymphocytic Leukemia (CLL)?
* Fevers * Night sweats * Unintentional weight loss
38
What is the treatment approach for early-stage Chronic Lymphocytic Leukemia (CLL)?
Early-stage 'watch and wait' strategy.
39
What are Myelodysplastic Syndromes (MDS)?
Disorders of the myeloid stem cell that may be asymptomatic or present with fatigue or illness.
40
What is the only cure for Myelodysplastic Syndromes (MDS)?
Hematopoietic stem cell transplantation (HSCT).
41
What are common assessments for leukemia patients?
* Health history * Symptoms (anemia, infection, bleeding, weakness, fatigue) * I&O's * Daily weights * Labs (Leukocyte count, ANC, Hematocrit, Platelets, Creatinine, Electrolytes, Coagulation tests, Hepatic function tests, Cultures)
42
What are common complications of leukemia?
* Infection * Bleeding (DIC) * Renal dysfunction * Tumor lysis syndrome
43
What is lymphopenia?
A condition where the lymphocyte count is less than 1500/mm³.
44
What are some causes of lymphopenia?
* Exposure to radiation * Long-term use of corticosteroids * Infections * Neoplasms * Alcohol abuse
45
What is Hodgkin Disease?
A relatively rare malignancy with a high cure rate, suspected viral etiology, and characterized by Reed-Sternberg cells.
46
What are the manifestations of Hodgkin Disease?
* Painless lymph node enlargement * Pruritus * B symptoms (fever, sweats, weight loss)
47
What is the incidence age for Hodgkin Disease?
Early 20s and again after the age of 50 years.
48
What characterizes Non-Hodgkin Lymphoma (NHL)?
It encompasses a diverse group of blood cancers that do not have Reed-Sternberg cells.
49
What is Multiple Myeloma?
A malignant disease of the most mature form of B lymphocyte—the plasma cell.
50
What are the common manifestations of Multiple Myeloma?
* Bone pain (80%) * Osteoporosis and fractures * Hypercalcemia * Renal impairment and failure * Anemia
51
What are the treatment options for Multiple Myeloma?
* HSCT * Chemotherapy * Corticosteroids * Radiation therapy * Immunomodulatory drugs, thalidomide analogs, monoclonal antibody