Hematology: Malignant Lymphoproliferative Flashcards

(42 cards)

1
Q

Slow uncontrollable growth of abnormal lymphoid cells in the BM, spleen and lymph nodes

Anemia, granulocytopenia, thrombocytopenia

A

Acute Lymphoblastic leukemia

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2
Q
  • Normocytic, normochromic anemia
  • CNS involvement with scrotal infiltration
  • Petechiae, purpura and/or hemorrhage (secondary to thrombocytopenia)
  • neg SBB, MPO
    + pos TdT, ACP, NSE
A

ALL

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3
Q

Most common type (74%) of childhood leukemia

best prognosis

A

L1

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4
Q

Burkitt type (Leukemic phase of Burkitt lymphoma)

A

L3

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5
Q

Lymphoblasts are very small & homogenous

Scanty cytoplasm (↑N/C ratio)

Nucleus is round and regular in shape with inconspicuous nucleoli

A

L1

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6
Q

Lymphoblasts are larger and variable (heterogenous) in size

Abundant, basophilic cytoplasm
Clefted nucleus with nucleoli present

A

L2: Large cell,
Heterogenous

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7
Q

Lymphoblast is large but varies little with size

Moderate and deeply basophilic cytoplasm often with vacuoles
Nucleus is round with 1-3 nucleoli

A

L3

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8
Q

Chronic disorder characterized by lymphadenopathy and infiltration of BM and peripheral blood by mature lymphocytes

More common among men, 40 to 60 y.o.

A

Chronic Lymphocytic Leukemia (CLL)

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9
Q

Most common early signs: enlarged lymph nodes, splenomegaly (and hepatomegaly later)

Bacterial infection is the major cause of death

AIHA in 10% of cases

A

CLL

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10
Q

-SMUDGE CELLS
-Hypogammaglobulinemia

A

CLL

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11
Q

RAI CLASS

+ thrombocytopenia

A

STAGE 4

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12
Q

Absolute lymphocytosis (>15 × 109/L) in the peripheral blood and BM

A

STAGE 0

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13
Q

80% are of the B cell type

typically shows large lymphocytes with moderately abundant cytoplasm, and prominent nucleoli

A

Prolymphocytic Leukemia

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14
Q

Leukemic Reticuloendotheliosi

lymphoproliferative disorder characterized by pancytopenia

Pancytopenia – most consistent laboratory observation

Normocytic, normochromic anemia

A

HCL

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15
Q

Monoclonal neoplastic proliferation of one of the cellular components of the lymphoid system

A

LYMPHOMA

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16
Q

LYMPHOMA DIAGNOSIS

A

LN BIOPSY

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17
Q

LYMPHOMA VS LEUKEMIA

A

LYMPHOMA = LOCALIZED, LYMPHOID
LEUKEMIA = SYSTEMIC, BM

18
Q

enlarged, painless, cervical lymph nodes

Reed-sternberg cells (OWL’S EYE)

INC ESR, LAP

19
Q

78%, lacunar cells IN HODGKIN’S IS WHAT

A

nodular sclerosis

20
Q

ann arbor stage where >2 lymph nodes on one side of the diaphragm

21
Q

ann arbor stage where lymph nodes on both sides of the diaphragm and spleen

22
Q

ann arbor stage where involves single lymph node region

23
Q

Proliferation of malignant lymphocytes that are arrested at certain stages of maturation (neoplasms of B cells and T/NK cells)

A

Non-Hodgkin’s Lymphoma

24
Q

causes skin itching, leading to ulcerative skin tumors

Lymphoid cells show a predilection for the epidermis (epidermotropism) and dermis and may spread to regional lymph nodes.

A

Mycosis Fungoides

25
Leukemic phase of mycosis fungoides T/NK , resembles monocyte Disseminated disease with widespread skin involvement (erythroderma), lymphadenopathy, and circulating lymphoma cells
Sēzary Syndrome
26
A B-cell neoplasm. t(8,21) Found most often in children in Africa & new guinea & commonly affects the jaw & facial bones;
Burkitt’s Lymphoma
27
Rapid growth and tumor cell death results in “starry sky” appearance of biopsy caused by macrophage cleaning the dead cells Tumor growth rate is the highest of any tumor (doubling each day)
Burkitt’s Lymphoma
28
Incidence of Hodgkin
Bimodal
29
Incidence of non Hodgkin
No pattern
30
Spread of Hodgkin
Predictable / Stepwise
31
Malignant proliferation of a monoclonal population of plasma cells that may or may not secrete detectable levels of a monoclonal immunoglobulin
PLASMA CELL DYSCRASIA
32
↑of one specific type of Ig produced by one neoplastic clone of plasma cells
Monoclonal gammopathy
33
Main clinical finding is bone pain (bone lesions/fractures) Renal failure (BJP toxic to tubular epithelial cells) and bacterial infection are the major cause of death
MM
34
Marked rouleaux; ↑ ESR Blue background to blood smear increase gamma band containing an M-spot which is composed of monoclonal CHONs
MM
35
MM + for BJP in urine. True or False.
True
36
Increased macroglobulins produce “hyperviscosity syndrome” which causes neurologic symptoms, CHF, visual impairment, nose/gum bleeding ALSO MARKED ROULEAUX AND ESR
Waldenström Macroglobulinemia
37
IMMUNOGLOBULIN IN MM
IgG
38
Malignant proliferation of lymphoid cells which produce incomplete Ig
Heavy Chain Disease
39
Mediterranean lymphoma
ALPHA HCD
40
resembles lymphoma, common in the elderly
Gamma HCD
41
resembles myeloma
Delta HCD
42
Generally found as an acute terminal stage in multiple myeloma 9 mos survival
Plasma Cell Leukemia