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A germinal center

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Title: A germinal center


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A germinal center
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B - cells
T - cells
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Malignant Lymphomas
  • Hodgkins Disease
  • Non - Hodgkins Lymphomas

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HODGKINS DISEASE
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Definition
  • Hodgkins Disease encompasses a group of
    disorders that differ from NHL by
  • Arise in a single node / chain of nodes spreads
    characteristically to contiguous lymph nodes
  • Reid - Sternberg cells

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Epidemiology
  • 50 of Malignant Lymphomas
  • Incidence is bimodal
  • Agent - EBV virus

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WHO Classification of HD
  • Nodular Sclerosis
  • Mixed Cellularity
  • Lymphocyte - rich
  • Lymphocyte depletion
  • Lymphocyte predominance

CLASSICAL HODGKINS
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Macroscopy
  • Enlargement of cervical nodes most frequent
  • Individual nodes discrete Rubbery
  • C/S grayish tan or pale tan

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Hodgkin Lymphoma - Gross
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Microscopy
  • RS cells in a appropriate background of
  • Non Neoplastic inflammatory cells--
    lymphocytes , plasma cells , eosinophils

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Reid - Sternberg cell
  • True neoplastic element in HD
  • Classic RS cells are large ,15 - 45 microns ,
    binucleate / bilobed
  • Nucleus contains large inclusion like owl eyed
    nucleoli surrounded by a clear halo.
  • Cytoplasm - abundant amphophilic

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Variants of RS cell
  • Mononuclear variant
  • Lacunar cells
  • L H variants

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R-S cell (Mononuclear variant)
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R-S cells (Lacunar variant)
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Lacunar cells
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R-S Cells - Multinucleate
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Lymphohistiocytic (L H) variant
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Mummified R-S cell
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SIGNIFICANCE OF DIFFERENT RS CELLS
  • Typical RS cell Lymphocyte depleted gt Mixed
    Cellularity gt Nodular Sclerosis gt Lymphocyte
    Predominant.
  • Lacunar Cell? Nodular Sclerosis
  • LH Cell (Pop Corn cell) ? Lymphocyte
    predominant.
  • Mummified cell? Classical HD

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Spread of HD Staging
  • Spread is predictable
  • Nodal disease precedes splenic disease
  • Splenic disease precedes liver disease
  • Liver disease precedes BM involvement extra
    nodal involvement.

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Liver that is involved with Hodgkin's disease
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ANN ARBOR CLASSIFICATION
  • STAGE DISTRIBUTION OF DISEASE
  • I. Involvement of a single lymph node region (I)
    or involvement of a single extra-lymphatic
    organ/site IE
  • II. Involvement of 2 /more LN regions on
    same side of diaphragm II or with
    involvement of limited contiguous
    extra-lymphatic organ /site IIE

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  • III. LN regions on both sides of diaphragm
    which may include spleen / limited contiguous
    EL organ /site .
  • IV. Disseminated foci of involvement.

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Nodular Sclerosis
  • 65 - 75
  • Characterized by
  • - Collagen bands
  • - Lacunar cells
  • - polymorphous background of
    lymphocytes , eosinophils , plasma cells
    macrophages
  • L cervical ,supraclavicular , mediastinal
  • women, adolescents, young adults.
  • Prognosis is Excellent

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HD - NS
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Mixed Cellularity
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  • classic RS cells mononuclear variants plentiful
  • diffuse effacement by a heterogeneous population
    of small lymphocytes , eosinophils , plasma cells
    , benign macrophages
  • Men , older age, B- symptoms , advanced tumor
    stage.

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HD - MC
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Lymphocyte Predominance
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  • Nodal effacement by vaguely infiltrate of small
    lymphocytes admixed with benign histiocytes
  • Classic RS cells few , L H variants common.
  • Men , lt 35 , limited disease
  • prognosis good.

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HD - lymphocyte predominance
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Hodgkins Lymphoma Lymphocyte depleted
  • Many Reed-Sternberg cells and variants are
    present.
  • This type of HD is not common.
  • Worst prognosis.

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Lymphocyte Depletion type
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Clinical Features
NHL
HD
  • single axial group multiple
    peripheral nodes
  • spread by contiguity non contiguous
    spread
  • mesenteric Waldeyers mesenteric Waldeyers
  • not involved
    involved
  • extranodal uncommon extranodal common

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NON - HODGKINS LYMPHOMAS
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NHL
  • 6th leading cause of cancer death
  • Recent increase especially in patients with AIDS
  • In 65 NHL arise in LN, 35 NHL arise in
    lymphoid tissue of parenchymal organs
  • Potential spread to other LN , Other tissues
    like liver, spleen, BM

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CLASSIFICATION
  • NHL may originate in T cells, B cells,
    histiocytes.
  • 80 - 85 B cell
  • Remainder - T cell
  • CD2, CD3, CD4, CD7, CD8 T cell
  • CD10, CD19, CD20, surface Ig B cell

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  • Many tumors of B cells may recapitulate
    the follicular pattern
  • Other B cell tumors , T cell tumors , histiocytic
    tumors - diffuse pattern
  • The morphologic changes reflect the stage of
    differentiation or activation at which the tumor
    cells are frozen

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CLASSIFICATIONS
  • The Working Formulation for Clinical Use
  • - LOW
  • - INTERMEDIATE
  • - HIGH GRADE
  • Each group is further divided based on
    architecture , cytologic appearance of cells
  • Also contains a miscellaneous group to include
    histiocytic T cell tumors

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REAL Classification
NHL
  • 1994 Revised European-American
  • classification of Lymphoid neoplasms,
  • Tumors of B cells
  • Tumors of T cells NK cells
  • Hodgkins Lymphoma

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WHO Classification of Lymphomas(1997)
  • Precursor B-cell neoplasms (neoplasms of
    immature B-cells),
  • Peripheral B-cell neoplasms (neoplasms of
    mature B-cells)
  • Precursor T-cell neoplasms (neoplasms of
    immature T-cells),
  • Peripheral T-cell and NK-cell neoplasms
    (neoplasms of mature T-cells natural killer
    cells),
  • Hodgkin Lymphoma (neoplasms of
  • Reed-Sternberg cells and variants)

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WHO classification
NHL
  • I. Precursor B cell Neoplasms
  • Precursor B Lymphoblastic
    Leukemia/Lymphoma

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WHO classification
NHL
  • II. Peripheral B-cell Neoplasms
  • Chronic lymphocytic leukaemia/small
    lymphocytic lymphoma,
  • B-cell prolymphocytic leukaemia,
  • Lymphoplasmacytic lymphoma,
  • Splenic and nodal marginal zone lymphomas,
  • Extranodal marginal zone lymphoma,
  • Mantle cell lymphoma,

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WHO classification
NHL
  • II. Peripheral B-cell Neoplasms
  • Follicular lymphoma,
  • Marginal zone lymphoma,
  • Hairy cell leukaemia,
  • Plasmacytoma/plasma cell myeloma,
  • Diffuse large B-cell lymphoma,
  • Burkitt's lymphoma

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WHO classification
NHL
  • III. Precursor T-cell Neoplasms
  • Precursor T-lymphoblastic leukaemia / lymphoma,

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WHO classification
NHL
  • IV. Peripheral T-cell and NK-cell Neoplasms
  • 1. T-cell prolymphocytic leukaemia,
  • Large granular lymphocytic leukaemia,
  • Mycosis fungoides/Sezary syndrome,
  • Peripheral T-cell lymphoma, unspecified,
  • Anaplastic large cell lymphoma,
  • Angioimmunoblastic T-cell lymphoma,

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WHO classification
NHL
  • IV. Peripheral T-cell and NK-cell Neoplasms
  • 7. Enteropathy-associated T-cell lymphoma,
  • 8. Panniculitis-like T-cell lymphoma,
  • 9. Hepatosplenic ?d T-cell lymphoma,
  • 10. Adult T-cell leukaemia/lymphoma,
  • 11. NK/T-cell lymphoma, nasal type,
  • 12. NK-cell leukaemia

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Immune markers
  • B-cells
  • CD10, CD19, CD20, CD21, CD23, CD79a,
  • T-cells
  • CD1, CD3, CD4, CD5, CD8

All Leukocytes CD45
NK-cells CD16, CD56
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Multiple enlarged lymph nodes high grade
non-Hodgkin's lymphoma (NHL) tends to involve a
single node.
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PRECURSOR B- AND T-CELL NEOPLASMS
  • Acute Lymphoblastic
  • Leukemia / Lymphoma

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Precursor B- and T-cell Neoplasms
  • ACUTE LYMPHOBLASTIC LEUKAEMIA / LYMPHOMA
  • Pre-B or Pre-T lymphocytes (lymphoblasts),
  • About 85 B-cell type childhood leukaemias
  • 15 T-cell lymphomas adolescent males,
  • Morphologically indistinguishable,
  • (immunophenotyping for subclassification)
  • Condensed chromatin, inconspicuous nuceloli,
    scant agranular cytoplasm

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ALL
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Pre-T cell lymphomas
  • ALLs with lymphomatous presentation,
  • Mediastinal masses (thymic involvement),
  • Lymphadenopathy and splenomegaly,
  • Same morphology as pre-B cell ALL,

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PERIPHERAL B-CELL NEOPLASMS- Chronic
lymphocytic leukaemia (CLL)/Small lymphocytic
lymphoma (SLL)
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PERIPHERAL B-CELL NEOPLASMS- Chronic
lymphocytic leukaemia (CLL)/Small lymphocytic
lymphoma (SLL)
  • Morphologically, phenotypically, and
    genotypically indistinguishable,
  • Differ in peripheral blood lymphocytosis,
  • Absolute lymphocyte count gt4000/cmm CLL
  • Most common leukemia of adults in west,
  • Less common in Asian countries,
  • SLL 4 of NHL,

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SLL - lymphnode
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SLL - LN
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Smudge cell
CLL
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CLL/SLL liver infiltration
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CLL/SLL Clinical features
  • Variable leucocyte count
  • - Leucopenia to gt 200,000/cmm.,
  • Disrupts immune function
  • - Susceptibility to infections,
  • - 10 to 15 - autoantibodies
  • (hemolytic anemia, thrombocytopenia)

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FOLLICULAR LYMPHOMA
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Follicular Lymphoma
  • Most common in US,
  • 45 of adult lymphomas,
  • Middle age,
  • Afflicts males and females equally,
  • Less common in Europe, rare in Asia,
  • Neoplastic cell germinal centre B-cells,

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ENLARGED MESENTERIC LYMPHNODES
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Mixture of Centrocytes and centroblasts
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