CHARACTERISTICSOF LLM Flashcards

(50 cards)

1
Q

WHAT ARE THE PROLIFERATIVE DISORDERS (2)

A

MYELOID

LYMPHOID

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2
Q

IS A DISEASE IN PERIPHERAL BLOOD AND BONE MARROW AND OVERPRODUCTION OF VARIOUS TYPES OF MATURE OR IMMATURE LEUKOCYTES

A

LEUKEMIA

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3
Q

GENERAL TERM FOR SOLID MALIGNANT TUMORS OF LYMPH NODES

A

LYMPHOMA

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4
Q

IS A FORM OF CANCER FROM PLASMA CELLS AND THE CELLS OVERGROW,FORMING A MASS OR TUMOR LOCATED IN THE BONE MARROW AND OVERPRODUCTION OF PLASMA CELLS IN BONE MARROW WITH PRODUCTION OF ABNORMAL PROTEINS

A

MYELOMA

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5
Q

WHAT ARE THE HEMATOLOGICAL MALIGNANCIES (3)

A

LEUKEMIA

LYMPHOMA

MYELOMA

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6
Q

WHAT ARE THE MARROW FAILURE (2)

A

APLASTIC ANEMIA

MYELODYSPLASIA

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7
Q

WHAT ARE THE CONDITIONS OF MAJOR MYELOPROLIFERATIVE NEOPLASM (MPNs)IN WHO CLASSIFICATION (5)

A

CHRONIC MYELOID LEUKEMIA (CML)

POLYCYTHEMIA VERA (PV)

ESSENTIAL THROMBOCYTHEMIA (ET)

PRIMARY MYELOFIBROSIS (PMF)

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8
Q

WHAT ARE THE CONDITIONS OF LEUKEMIA (4)

A

CHRONIC MYELOID LEUKEMIA (CML)

CHRONIC LYMPHOCYTIC LEUKEMIA (CLL)

ACUTE MYELOID LEUKEMIA (AML)

ACUTE LYMPHOBLASTIC LEUKEMIA (ALL)

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9
Q

2 TYPES OF ACUTE LYMPHOBLASTIC LEUKEMIA

A

B CELL ACUTE LYMPHOCYTIC LEUKEMIA (B-ALL)

&

T CELL ACUTE LYMPHOCYTIC LEUKEMIA (T-ALL)

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10
Q

WHAT ARE THE 4 TYPES OF B CELL ACUTE LYMPHOCYTIC LEUKEMIA

A

PRE-CURSER B CELL ACUTE LYMPHOCYTIC LEUKEMIA

PRO B-ALL B CELL ACUTE LYMPHOCYTIC LEUKEMIA

MATURE B CELL ACUTE LYMPHOCYTIC LEUKEMIA

COMMON B CELL ACUTE LYMPHOCYTIC LEUKEMIA

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11
Q

WHAT ARE THE 2 TYPES OF LYMPHOMA

A

HODGKIN LYMPHOMA

NON-HODGKIN LYMPHOMA

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12
Q

WHAT ARE THE TYPES OF HODGKIN LYMPHOMA (2)

A

CLASSICAL HODGKIN LYMPHOMA

NON-CLASSICAL HODGKIN LYMPHOMA

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13
Q

CONDITION OF CLASSICAL HODGKIN LYMPHOMA (4)

A

NODULAR SCLEROSING

MIXED CELLULARITY

LYMPHOCYTE RICH

LYMPHOCYTE DEPLETED

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14
Q

CONDITION OF NON CLASSICAL HODGKIN LYMPHOMA (1)

A

NODULAR LYMPHOCYTE-PREDOMINANT

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15
Q

CONDITIONS OF B CELL NON HODGKIN LYMPHOMA (6)

A

BURKITT LYMPHOMA

DIFFUSE LARGE B-CELL LYMPHOMA

FOLLICULAR LYMPHOMA

MANTLE CELL LYMPHOMA

MARGINAL ZONE LYMPHOMA

PRIMARY CNS LYMPHOMA

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16
Q

WHAT ARE THE 2 TYPES OF NON-HODGKIN LYMPHOMA

A

B CELL NON HODGKIN LYMPHOMA

T CELL NON HODGKIN LYMPHOMA

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17
Q

CONDITIONS OF T CELL NON HODGKIN LYMPHOMA (2)

A

ADULT T CELL LYMPHOMA

MYCOSIS FUNGOIDES

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18
Q

clonal hematopoietic stem cell disorders caused by genetic mutations leading to abnormal proliferation and accumulation of erythrocytes, granulocytes, and/or platelets.

A

MYELOPROLIFERATIVE NEOPLASMS

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18
Q

WHAT ARE THE OTHER WHO RECOGNIZED MYELOPROLIFERATIVE NEOPLASMS (4)

A

CHRONIC NEUTROPHILIC LEUKEMIA (CNL)

CHRONIC EOSINOPHILIC LEUKEMIA (CEL)

MASTOCYTOSIS

MYELOPROLIFERATIVE NEOPLASM UNCLASSIFIED

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19
Q

PATHOGENESIS OF MYELOPROLIFERATIVE NEOPLASM

Caused by _________ or _______ from normal cytokine regulation.

Affects _______, _______, and other _____ variably.

A

HYPERSENSITIVITY OR INDEPENDENCE

BONE MARROW, PERIPHERAL BLOOD AND TISSUES

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20
Q

IS A STABE CHRONIC DISORDER

Progress to ________

Enter a _____ or ______ phase (marrow failure).

Transition through _____phases to more aggressive stages.

A

ACUTE LEUKEMIAS

DEPLETED OR HYPOPLASTIC

SUBACUTE

21
Q

Occur in families with multiple affected members, indicating possible inherited predisposition.

A

FAMILIAL MYELOPROLIFERATIVE NEOPLASMS

22
Q

caused by a single genetic translocation in a pluripotent hematopoietic stem cell.

A

MYELOPROLIVERATIVE NEOPLASM (MPN)

23
Q

Characterized by the _________ resulting from t(__,__)(__,__) translocation, creating the ________ fusion gene.

A

CHRONIC MYELOGENOUS LEUKEMIA

PHILADELPHIA CHROMOSOME

t(9,22) and q(34) q(11)

BCR-ABL1

24
3 PHASES OF CHRONIC MYELOGENOUS LEUKEMIA
CHRONIC PHASE (INITIAL STAGE) ACCELERATED PHASE ( AFTER 3-4 YEARS IF UNTREATED) BLAST CRISIS (RESEMBLES ACUTE LEUKEMIA)
25
CHRONIC MYELOGENOUS LEUKEMIA OCCURS IN ADULT AGED ______ SLIGHT ____PREDOMINANCE PRE-IMATINIB RATE: ____DEATHS PER _______/YEAR
46-53 YEARS OLD MALE 1.5; 100,000
26
SIGN & SYMPTOMS OF CHRONIC MYELOGENOUS LEUKEMIA (6)
FATIGUE REDUCED EXERCISE TOLERANCE ANOREXIA WEIGHT LOSS ABDOMINAL DISCOMFORT SYMPTOMS DUE TO SPLENOMEGALY
27
IS A CLONAL MYELOPROLIFERATIVE NEOPLASM (MPN). Characterized by ________ (increased erythrocytes, granulocytes, and platelets in blood). Arises from a __________. __________ cells in PV are _______ to or ______ of erythropoietin (EPO). Common clinical finding: _______.
POLYCYTHEMIA VERA PANMYELOSIS HEMATOPOIETIC STEM CELL SPLENOMEGALY ERYTHROID PROGENITOR; HYPERSENSITIVITY OR INDEPENDENT
28
Discovered in _____, found in 90–97% of PV patients. Mutation in exon 14: _____ → _____ causing ______to be replaced by _____ at ______ Occurs in the ___________ Prevents folding into ________ Leads to constitutive activation of _____ without _____ •Drives _______ cell proliferation.
JAK2 V617F MUTATION 2005 GUANINE-THYMINE; VALINE; PHENYLALANINE; CODON 617 JAK2 TYROSINE KINASE GENE INACTIVE STATE JAK2; ERYTHROPOIETIN (EPO)
29
2 PHASES OF POLYCYTHEMIA VERA
PROLIFERATIVE (STABLE) PHASE (EARLY ACTIVE PHASE) SPENT PHASE ( LATE PHASE)
30
WHICH PHASE OF POLYCYTHEMIA VERA IS THIS Increased ________ (hallmark of PV) •Overproduction of ____, ____, and ____ •Occurs ______of normal regulatory controls
PROLIFERATIVE (STABLE) PHASE RED CELL MASS RBCs, WBCs and PLATELETS INDEPENDENT
31
WHICH PHASE OF POLYCYTHEMIA VERA IS CHARACTERIZED BY Progressive splenomegaly or hypersplenism Pancytopenia (reduction in all three blood cell lines) Bone marrow fibrosis (myelofibrosis) Ineffective hematopoiesis Morphologic shift toward postpolycythemic myeloid metaplasia
SPENT PHASE
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