Malignant Lymphomas and Hodgkin's Disease Flashcards

1
Q

Describe the features of Precursor B lymphoblastic leukemia/lymphoma.

A
  • agressive
  • particularly occur in childhood
  • TdT positive
  • related to B cell ALL
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2
Q

Describe the features of B small lymphocytic lymphoma/B cell CLL.

A
  • Diffuse, uniform, small lymphocytes
  • long survival, but difficult to cure by chemotx
  • tissue equiv of CLL, often involves multiple nodes, spleen
  • prolymphocytic varieties, include larger cells and may be more agressive
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3
Q

Describe the features of Lymphoplasmacytic Lymphoma.

A
  • similar to small lymphocytic lymphomas but shows plasmacytoid differentiation. slow growing
  • IgM monoclonal spike, may have hyper viscosity: Waldenstrom’s Macroglobulinemia
  • pay have t(9;14) Pax 5 gene-b cell specific activating protein
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4
Q

Describe the features of Mantle Cell Lymphoma

A
  • mantle zone cells (periphery of follicles)
  • agressive
  • t(11;14), bcl-1 genes for cyclin D1, upregulated, promotes G1 to S transition in cell cycle
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5
Q

Describe the features of follicular center cell (FCC) lymphomas.

A

-one of most common forms of B cell lymphoma
-forms follicle like nodules
-t(14;18) translocation, with increased bcl2 protein, inhibits apoptosis
-B cell markers +CD10
-the more large cells, the more aggressive
Grade 1: small cell type–very few large cells
-mainly small lymphocytes with nuclei showing deep cleaves
-most have follicular pattern
-marrow involvement is detectable in over 70% at presentation
-few cells in S phase so cure difficult
Grade 2/3 mixed small and large cell types
-may progress to diffuse large cell lymphomas

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6
Q

Describe the features of marginal zone lymphoma.

A
  • called MALToma in GI tract (MALT=mucosa associated lymphoid tissue)
  • some MALTomas are on the borderlands of hyperplasias and respond to antibiotic tx, means that proliferation is antigen driven.
  • contain many plasma cells and blur with lymphoplasmacytic lymphoma
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7
Q

Describe the features of plasma cell (multiple myeloma).

A
  • in bone marrow, multiple lytic lesions, usually not in nodes
  • typically shows monoclonal Ig spike in serum
  • plasma cell is the end stage fully differentiated effector B cell
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8
Q

Describe the features of large B cell lymphoma. (DLBCL)

A
  • includes large B cell immunoblastic large cells containing prominent nucleoli, and abundant cytoplasm. Prognosis untreated is poor, may respond well to chemo tx
  • some show t(14;18)
  • some show bcl-6 gene defects
  • common, about 30% of adult lymphomas
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9
Q

Describe the features of Burkitt lymphoma

A
  • agressive, one of most common lymphomas of children
  • endemic in africa and new guinea, assoc with malaria & EBV
  • t(8;14), myc oncogene
  • Starry night appearance
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10
Q

Describe the features of precursor T- T lymphoblastic leukemia/lymphoma.

A
  • children and young adults, esp males
  • present often as mediastinal mass, then becomes leukemic
  • diffuse proliferation of primitive cells resembling embryonic T lymphoblasts
  • have high mitotic rate, aggressive
  • related to T cell ALL
  • Express TdT and T cell markers
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11
Q

Describe peripheral T cell lymphoma

A
  • various appearances; probably more than one disease type, CD3 phenotype useful in diagnosis
  • may resemble diffuse large B cell lymphoma, from which they must be distinguished via CD3 v. CD20
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12
Q

Describe cutaneous T cell lymphomas, including mycosis fungicides.

A
  • small cells with folded nuclei
  • frequently composed of cells with T helper CD4
  • related to leukemia like condn Sezary syndrome
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13
Q

Describe Adult T cell lymphoma/leukemia

A

uncommon

-japan, africa, caribbean, HTLV1 related

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14
Q

Describe anapestic large cell lymphoma- ALCL

A
  • CD30+ cells
  • t(2,5) translocation, npm/alk gene
  • cutaneous variant, less aggressive than nodal form
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15
Q

What are the general pathologic features of Hodgkin lymphoma?

A
  • Reed Sternberg cells: owl face
  • also have large mononuclear cells
  • RS cells mixed with lymphocyte,s plasma cells, histiocytes, eosinophils, neutrophils, fibroblasts “reactive”
  • if assoc with B symptoms (due to RS secreting cytokines): night sweats, fever, wt loss: poor prognosis
  • markers: CD15+ and CD30+
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16
Q

Describe lymphocyte predominant Hodgkin lymphoma.

A
  • many lymphocytes and only a few RS cells
  • usually in nodular form
  • contains polypoid variants of RS cell with lobulated nuclei
  • markers: CD45 and CD20
17
Q

Describe Classical hodgkin lymphoma: nodular sclerosing Hodgkin lymphoma.

A
  • broad bands of collagen circumscribing nodules of neoplastic tissue
  • large RS cell variants are characteristic
  • usually presents as early stage disease and has a slow progression
  • young women are particularly affected and mediastinal involvement is common
18
Q

Describe Classical hodgkin lymphoma: lymphocyte rich HL.

A

numerous lymphocytes, few RS cells

19
Q

Describe Classical hodgkin lymphoma: mixed cellularity (MC) HL.

A

intermediate histologic appearance with many lymphocytes, plasma cells, eosinophils, and RS cells
-prognosis is intermediate

20
Q

Describe Classical hodgkin lymphoma: lymphocyte-depleted (LD) HL

A
  • very many reed-sternberg cells, few lymphocytes
  • has worst prognosis and typically presents as stage III or IV disease
  • very rare