CLL/SLL |
B cell prolymphocytic leukemia |
Splenic B cell marginal zone lymphoma |
Hairy cell leukemia |
Splenic B cell lymphoma / leukemia |
Lymphoplasmacytic lymphoma |
Heavy chain disease |
Plasma cell neoplasms |
Extranodal marginal zone lymphoma of mucosa associated lymphoid tissue |
Nodal marginal zone lymphoma |
Follicular lymphoma |
Primary cutaneous follicle center lymhoma |
Mantle cell lymphoma |
Diffuse large B cell lymphoma |
DLBCL associated with chronic inflammation |
Lymphomatoid granulomatosis |
Primary mediastinal large B cell lymphoma |
Intravascular large B cell lymphoma |
ALK positive large B cell lymphoma |
Plasmablastic lymphoma |
Large B cell lymphoma - HHV8 associated multicentric Castleman |
Primary effusion lymphoma |
Burkitt lymphoma |
B cell lymphoma, unclassifiable with features of DLBCL and Burkitt |
B cell lymphoma, unclassifiable with features of DLBCL and Hodgkin |
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Article |
Notes |
Simultaneous presence of t(11;14) and a variant Burkitt's translocation in
the terminal phase of a mantle cell lymphoma. |
t(11;14)(q13;q32) and t(2;8)(p12;q24) |
Increased number of chromosomal imbalances and high-level DNA amplifications
in mantle cell lymphoma are associated with blastoid variants. |
P53,
P16(INK4a), RB, C-MYC, N-MYC, BCL2, BCL6, CDK4, and BMI-1 |
Cytogenetic findings in mantle cell lymphoma cases with a high level of
peripheral blood involvement have a distinct pattern of abnormalities. |
Chromosomes 1,
3, 7, 8, 9, 10, 12, 15, 17, and 21 |
Loss of a novel tumor suppressor gene locus at chromosome 8p is associated
with leukemic mantle cell lymphoma. |
Chromosome 8p |
Blastic mantle cell lymphoma associated with Burkitt-type translocation and
hypodiploidy. |
t(11;14),
t(8;14), t(1;19), dup(8)(q24q13) |
Mantle cell lymphoma with 8q24 chromosomal abnormalities: a report of 5
cases with blastoid features. |
t(11;14),
(8;14)(q24;q32), (2;8)(q13;q24), add(8)(q24) |
Coexistence of BCL1/CCND1 and CMYC aberrations in blastoid mantle cell
lymphoma: a rare finding associated with very poor outcome. |
t(11;19;14)(q13;q13;q32), (8;22)(q24;q11), trisomy 8 |
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