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Definition
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Follicular lymphoma genetics |
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Definition
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Burkitt lymphoma genetics |
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Definition
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Mantle cell lymphoma genetics |
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Definition
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Definition
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Mantle cell lymphoma CyclinD1 |
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Definition
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Role of primary/central lymphoid tissue |
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Definition
Help grow B/T precursors to naïve state B: BM, T: thymus |
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Role of secondary/peripheral lymphoid tissue |
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Definition
Allow Ag-cell interaction LN, spleen, MALT |
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Definition
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Definition
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Ag-independent phase: location, result, morphology |
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Definition
Primary/central lymphoid tissue Mature but naïve Small cells w/ dense chromatin |
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Ag-dependent phase: location, cellular transformation |
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Definition
Secondary/peripheral lymphoid tissue Cell inc. cyto, disperses chromatin, gains nucleolus Form germinal centers = centroblasts/non-cleaved, lose BCL2 Mutate Ig variable region = centrocyte Good fit = BCL2 comes back, b/c memory/plasma cells Bad fit = apoptosis |
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Causes of lymphocytopenia |
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Definition
Congenital immunodeficiency HIV Cytotoxic drugs like chemo |
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Reactive causes of lymphocytosis |
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Definition
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Neoplastic causes of lymphocytosis |
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Definition
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Characteristics that differentiate neoplastic lymphocytosis from reactive (3) |
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Definition
Sustained WBC >30,000 Clonal |
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Mono: pathogenesis, symptoms |
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Definition
EBV in saliva infects oropharynx B cells, disseminates to lymphoid tissue |
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Mechanisms that control mono |
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Definition
CD8 T cells, NK cells EBV-specific and non-specific Ab |
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Mono morphology: peripheral, lymph node |
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Definition
Reactive/atypical lymphocytes Paracortical hyperplasia |
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Definition
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Term
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Definition
Middle-aged to older Usually asymptomatic Anemia, weight loss Lymphadenopathy Hepatosplenomegaly Hypogammaglobulinemia |
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CLL morphology: peripheral, BM, LN |
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Definition
Homogenous small mature cells w/ condensed chromatin, smudge cells BM: diffuse infiltrate LN: diffuse infiltrate |
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Term
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Definition
19, 20 5+ 23+ Dim surface Ig |
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Term
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Definition
Trisomy 12 Del. 13, 11, 17 |
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Term
CLL is different from SLL b/c… |
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Definition
CLL mainly works in BM and blood SLL mainly works in LN |
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Definition
Indolent but incurable Prone to infections Prolymphocytic transformation Large cell transformation |
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HCL: age range, sex, symptoms (usually symptomatic) |
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Definition
Older men Fatigue Recurrent infection Splenomegaly, abdominal discomfort |
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HCL morphology: peripheral, BM, spleen |
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Definition
Pancytopenia, hairy cells BM: fried egg infiltration + fibrosis (dry tap) Spleen: red pulp infiltration forming blood lakes |
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Definition
TRAP+ 11+ 25+ 103+ Strong surface Ig |
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Term
Acute bacterial and viral infections show ___ hyperplasia |
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Definition
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Causes of chronic follicular hyperplasia (3) |
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Definition
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Causes of paracortical hyperplasia (3) |
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Definition
Mono Drug sensitivity reactions SLE |
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Term
Plasma cell neoplasm Ig secretion is abnormal because… (2) |
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Definition
Usually light chain produced in excess Monoclonal |
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Term
Monoclonal Ig: characteristics and consequences |
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Definition
Abnormal chem: deposits in tissues Hyperviscous: blurry vision, headache, dizziness, deafness Cryoglobulinemia: ppt at colder temps Interfere w/ fibrin polymerization: bleeeding |
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Information obtained from SPEP or UPEP |
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Definition
Monoclonal M spike, usually in gamma region Other Ig are reduced |
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Information obtained from IFE |
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Definition
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Definition
Free light chains in urine Toxic to renal cells |
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Multiple myeloma: age range, sex, race, symptoms |
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Definition
Older black males Calcium inc. Renal insuffiency Anemia Bone lesions |
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Term
Multiple myeloma: pathogenesis, prognosis |
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Definition
Infiltrate bone, plasma cell cytokines cause resorption Light chains deposit in kidneys Fxl hypogammaglobulinemia leads to infections (CMI is fine) Poor, chemo extends it to 3 yrs |
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Term
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Definition
Hypercalcemia Inc. BUN, creatinine Inc. serum protein, proteinuria M spike >3 g/dL |
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Multiple myeloma: protein composition |
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Definition
IgG (hyperviscous) Free light chain Amyloid |
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Term
Multiple myeloma: peripheral, BM |
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Definition
Anemia, rouleaux BM: >30% infiltration w/ abnormal plasma cells w/ fine chromatin and possibly nucleoli |
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Term
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Definition
No CRAB, no lytic lesions M spike <3 g/dL BM: <10% plasma cell infiltration |
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Term
MGUS: age range, clinical course, tx |
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Definition
Older 25% have stable levels of monoclone 25% have rising levels, but it's not neoplastic 25% develop overt neoplasm 25% die of other causes Tx: none required |
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Term
Plasmacytoma: symptoms, BM |
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Definition
No CRAB, single lesion BM: single mass of neoplastic cells |
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Term
Plasmacytoma, solitary: location, progression |
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Definition
Intramedullary mass 55% progress to multiple myeloma |
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Term
Plasmacytoma, extraosseous: location, progression |
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Definition
Oronasopharynx, sinuses 15% progress to multiple myeloma |
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Term
Are lymphoplasmacytic lymphomas and Waldenstrom's macroglobulinemias true neoplasms? What are they? Where are they? |
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Definition
No! They're lymphomas w/ plasma cell differentiation BM sometimes LN, spleen |
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Term
Waldenstrom macroglobulinemia is ___ + ___ + ___ |
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Definition
Lymphoplasmacytic lymphoma IgM monoclone Hyperviscocity syndrome |
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Waldenstrom macroglobulinemia: symptoms |
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Definition
Visual impairment, headache, dizziness, deafness Cryoglobulinemia Lymphadenopathy Hepatosplenomegaly Anemia, bleeding No lytic lesions |
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Waldenstrom macroglobulinemia morphology: LN |
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Definition
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Waldenstrom macroglobulinemia: prognosis, tx |
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Definition
4 years Plasmapheresis alleviates symptoms |
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Term
Amyloid: composition, gross and histo appearance, stain |
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Definition
Amyloid light chain (or AA) protein Gross: waxy, white appearance Histo: hyaline looking Congo red: green birefringence |
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Term
Primary systemic amyloidosis: cause |
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Definition
Underlying plasma cell neoplasm secreting AL |
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Secondary systemic amyloidosis: cause |
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Definition
Underlying inflammatory condition, AA protein not AL |
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