Leukemia, Lymphoma, & Anemia Flashcards

AML, ALL, CML, CLL, Hodgkin, Non-Hodgkin, Anemia

1
Q

What is leukemia?

A

A malignant disorder of hematopoietic stem cells, leading to excessive proliferation of abnormal white blood cells in the bone marrow, which interferes with normal hematopoiesis​

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2
Q

What are the main types of leukemia?

A

Acute lymphocytic leukemia (ALL) – Common in children, rapid progression.

Acute myeloid leukemia (AML) – Affects both children and adults, poor prognosis in elderly.

Chronic lymphocytic leukemia (CLL) – Common in older adults, slow progression.

Chronic myeloid leukemia (CML) – Associated with the Philadelphia chromosome (t9;22), progresses from chronic to blast crisis phase.

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3
Q

What are common symptoms of leukemia?

A

Anemia (fatigue, pallor), thrombocytopenia (easy bruising, bleeding), frequent infections, bone pain, hepatosplenomegaly, and weight loss

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4
Q

What is the hallmark genetic mutation in CML?

A

BCR-ABL fusion gene due to Philadelphia chromosome (t9;22)​

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5
Q

What are the laboratory findings in leukemia?

A

Elevated or reduced WBC count, anemia, thrombocytopenia, blast cells in peripheral blood, and possible chromosomal abnormalities (e.g., t(9;22) in CML).

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6
Q

What is the Philadelphia chromosome, and which leukemia is it associated with?

A

The Philadelphia chromosome (t(9;22), BCR-ABL fusion gene) is associated with Chronic Myeloid Leukemia (CML), leading to increased tyrosine kinase activity.

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7
Q

How is leukemia diagnosed?

A

Blood test (CBC): Increased or decreased WBCs, anemia, thrombocytopenia.

Bone marrow biopsy: Confirms leukemic blast cells.

Cytogenetic analysis: Detects chromosomal abnormalities (e.g., Philadelphia chromosome in CML).

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8
Q

How is leukemia treated?

A

Chemotherapy (first-line for acute leukemias).

Targeted therapy (e.g., imatinib for CML).

Bone marrow transplant for severe cases.

Supportive therapy (blood transfusions, antibiotics)

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9
Q

What is the most common leukemia in children?

A

Acute lymphocytic leukemia (ALL)​

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10
Q

What is lymphoma?

A

Lymphoma is a malignancy of lymphoid tissue, affecting lymphocytes and the immune system. It primarily occurs in lymph nodes but can involve extranodal sites.

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11
Q

What are the two major types of lymphoma?

A

Hodgkin Lymphoma (HL) – Characterized by Reed-Sternberg cells.

Non-Hodgkin Lymphoma (NHL) – A heterogeneous group of lymphoid malignancies, including diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma.

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12
Q

What is the key histological marker of Hodgkin lymphoma?

A

Reed-Sternberg cells (large, binucleated B-cells)

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13
Q

What are symptoms of lymphoma?

A

Painless lymphadenopathy - often in the neck, night sweats, fever, weight loss (“B symptoms”), pruritus, hepatosplenomegaly.

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14
Q

What is the most common type of non-Hodgkin lymphoma (NHL)?

A

Diffuse large B-cell lymphoma (DLBCL)​

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15
Q

What infections are associated with lymphoma?

A

Epstein-Barr virus (EBV) → Hodgkin lymphoma, Burkitt lymphoma.

Helicobacter pylori → Gastric MALT lymphoma

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16
Q

What is the characteristic histological finding in Hodgkin Lymphoma?

A

Reed-Sternberg cells – large, binucleated or multinucleated cells with prominent nucleoli (“owl’s eye appearance”).

17
Q

How is lymphoma diagnosed?

A

Lymph node biopsy, immunophenotyping, flow cytometry, PET/CT scan, bone marrow biopsy.

18
Q

What is the Ann Arbor staging system used for?

A

It is used to the staging of lymphoma based on lymph node involvement and systemic symptoms:

Stage I: Single lymph node region.

Stage II: Two or more lymph node regions on the same side of the diaphragm.

Stage III: Lymph nodes on both sides of the diaphragm.

Stage IV: Disseminated disease.

19
Q

What is the characteristic translocation in Burkitt lymphoma?

A

t(8;14) → c-MYC overexpression​

20
Q

How is lymphoma treated?

A

Hodgkin Lymphoma: ABVD chemotherapy (Adriamycin, Bleomycin, Vinblastine, Dacarbazine), radiation therapy.

Non-Hodgkin Lymphoma: Chemotherapy (e.g., CHOP regimen – Cyclophosphamide, Doxorubicin, Vincristine, Prednisone), immunotherapy (e.g., Rituximab for B-cell NHL).

21
Q

How does NHL differ from HL in terms of spread?

A

NHL spreads non-contiguously (randomly) while HL spreads contiguously (from one node to the next)

22
Q

What is anemia?

A

A condition characterized by a reduced number of RBCs or decreased hemoglobin, leading to impaired oxygen transport​

23
Q

What are the four primary causes of anemia?

A

1) Blood loss (acute trauma, chronic GI bleeding).

2) Increased RBC destruction (hemolytic anemia).

3) Decreased RBC production (iron deficiency, bone marrow failure).

4) Nutritional deficiencies (B12, folate, iron)

24
Q

What is the most common anemia worldwide?

A

Iron deficiency anemia​

25
What are common symptoms of anemia?
Fatigue, pallor, shortness of breath, tachycardia, dizziness, cold intolerance, spoon-shaped nails (koilonychia in iron deficiency anemia), glossitis.
26
What are key laboratory findings in iron deficiency anemia?
- Low MCV (microcytic anemia) - Low ferritin, high TIBC - Hypochromic RBCs with increased central pallor
27
What are three major manifestations of anemia?
1) Fatigue, pallor, tachycardia (due to decreased oxygen transport). 2) Dyspnea, dizziness (due to tissue hypoxia). 3) Glossitis, brittle nails (koilonychia) in iron deficiency
28
What are characteristics of hemolytic anemia?
1) Premature RBC destruction. 2) Increased reticulocyte count (bone marrow compensation). 3) Jaundice (due to increased bilirubin from RBC breakdown)​
29
What causes vitamin B12 deficiency anemia?
Dietary deficiency (vegans) Pernicious anemia (autoimmune destruction of parietal cells, leading to lack of intrinsic factor) Malabsorption (Crohn’s disease, gastric bypass)
30
How does B12 deficiency anemia differ from iron deficiency anemia?
B12 deficiency → Megaloblastic anemia (large RBCs), neurological symptoms (paresthesias). Iron deficiency → Microcytic anemia (small RBCs), pallor, fatigue​
31
What is the main treatment for iron deficiency anemia?
Oral ferrous sulfate (iron supplement), dietary changes, treating underlying cause (e.g., GI bleeding)​
32
Why do pregnant women need more iron?
Increased demand for fetal erythropoiesis and maternal blood volume expansion​.