PCD Flashcards

(50 cards)

1
Q

mature B cell capable of synthesizing antibodies

A

PLASMA CELL

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2
Q

are proteins with gamma electrophoretic mobilities that are synthesized in response to an antigen

A

ANTIBODIES (IMMUNOGLOBULINS or g GLOBULINS) –

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3
Q

Activators of classical complement pathway

A

IgG

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4
Q

Hemaglutinins

Hemolysins

A

IgG

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5
Q

Most common (80%)

A

IgG

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6
Q

Precipitating antibody

Virus-neutralizing antibody

A

IgG

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7
Q

Synthesized by plasma cells found in the respiratory and GI tracts and most excretory organs

A

IgA

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8
Q

First line of defense for mucosal surfaces

A

IgA

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9
Q

Second most abundant (10-15%)

A

IgA

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10
Q

First antibody to appear in response to an antigenic challenge

A

IgM

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11
Q

Circular pentameric arrangement

A

IgM

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12
Q

Largest antibody

A

IgM

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13
Q

5-10% of circulating antibodies

Localized in blood

A

IgM

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14
Q

“Ragweed” antibody

A

IgD

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15
Q

Trace concentrations

A

IgD

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16
Q

MW = 140,000 daltons

A

IgD

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17
Q

Functions in lymphocytic activation and suppression

A

IgD

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18
Q

Mediates allergic reactions and parasitic infections

A

IgE

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19
Q

Attaches to mast cells and basophils

A

IgE

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20
Q

“Reagenic antibody”

A

IgE

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21
Q

detects imbalance of Ig of free H or L chains

A

IMMUNOELECTROPHORESIS and IMMUNOFIXATION ELECTROPHORESIS

22
Q

Most common disease of plasma cells

A

MULTIPLE MYELOMA

23
Q

MULTIPLE MYELOMA

Predisposing factors

A

Genetics

Chronic antigenic stimulation

24
Q

Begins in the bone marrow with lytic bone diseases and osteoporosis

A

MULTIPLE MYELOMA

25
Igs produced are mostly of the _ class (50%) or _ (20%) or L-chains only __ (15%) or _ (25%)
IgG IgA (Bence-Jones Protein) Amyloid
26
CLINICAL PRESENTATION
HyperCalcemia Renal insufficiency Anemia Bone lesions
27
LABORATORY FINDINGS
N/N anemia ESR elevated due to increased globulins Rouleaux formation Few abnormal plasma cells BM = 10-15% plasmacytes Urinary protein (strip and SSA) – not sensitive due to their specificity to albumin (+) casts – hyaline or tubular epithelial casts Electrophoresis – monoclonal peak Hyperuricemia Hypercalcemia Radiologic exams
28
MYELOMA CELL CHARACTERISTICS
Large with immature appearing chromatin OR small with clumped chromatin Pale or dark (depending on cytoplasmic RNA) Sometime bizarre and multinucleated or lobulated nuclei Inclusions
29
Accumulations of Igs in the cisternae
MOTT CELL, MORULA CELL or PLASMA CELL WITH RUSSELL BODIES
30
intranuclear inclusions
DUTCHER BODIES –
31
Circulating plasma cell levels > 2 X 109/L (0.14-0.20 NV)
PLASMA CELL LEUKEMIA
32
PLASMA CELL LEUKEMIA
Younger patients Less bone pain Less osteolysis Greater incidence of lymphadenopathy and hepatosplenomegaly Pancytopenia with leukoerythroblastic findings Elevated ESR Abnormal plasma cells are smaller with little cytoplasm and pronounced N:C asynchronism BM infiltration is diffuse (45%)
33
A lymphoproliferative disorder characterized by large concentrations of monoclonal IgM (>15%)
WALDENSTROM MACROGLOBULINEMIA
34
The abnormal B lymphocytes arise from the extramedullary nodes and have the ability to differentiate to large plasmacytoid lymphocytes and plasma cells
WALDENSTROM MACROGLOBULINEMIA
35
Rarely causes osteolytic lesions
WALDENSTROM MACROGLOBULINEMIA
36
Glomerular lesions caused by deposition of IgM complexes of amyloid
WALDENSTROM MACROGLOBULINEMIA
37
Affects men >50 years old with hepatosplenomegaly, lymphadenopathy and retinal abnormalities
WALDENSTROM MACROGLOBULINEMIA
38
WALDENSTROM MACROGLOBULINEMIA LABORATORY FINDINGS
N/N Reticulocytes dec. or N Normal WBC and platelets BM- plasmacytoid lymphoma (+) Mast cells – CLUE!
39
Autoimmune hemolytic anemia
Raynaud’s phenomenon (anti-G) Cold agglutinin (anti-i)
40
WALDENSTROM MACROGLOBULINEMIA platelet function fibrinogen thrombin time plasma viscosity Monoclonal IgM with cryoglobulin activity
Abnormal platelet function Thrombocytosis (maybe plasma precipitates) Low fibrinogen Prolonged thrombin time Increased plasma viscosity – precipitation or gel formation at 4C Electrophoresis
41
A rare disease characterized by abnormal synthesis of Fc fragment of a particular H chain particularly a (most common), g and m
HEAVY CHAIN DISEASE
42
Resembles activated lymphocytes and plasma cell | Lymphoma like symptoms
HEAVY CHAIN DISEASE
43
HCD characterized by infiltration of plasmacytoid lymphocytes into the duodenal and jejunal walls producing malabsorption and abdominal distress and respiratory tracts
ALPHA HCD
44
HCD Found in older men and presents with a malignant lymphoma with fever, erythema, lymphadenopathy and hepatosplenomegaly
GAMMA HCD
45
HCD Rarest; associated with CLL
MU HCD
46
A condition in which proetinaceous deposits (amyloid) occur throughout the body
AMYLOIDOSIS
47
closely associated with monoclonal gammopathies such as plasma cell myeloma
PRIMARY AMYLOIDOSIS
48
associated with chronic illnesses and amyloid unrelated to Ig
SECONDARY AMYLOIDOSIS
49
AMY Electron microscopy and Xray diffraction
amyloid is in the Beta pleated sheet formation
50
AMY Polarizing microscopy with Congo red
apple green birefringence