Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1996-7-15
pubmed:abstractText
Large-cell variants are uncommon in mantle cell lymphoma (MCL). Here we describe the pathologic and clinical findings in five patients with large-cell lymphoma related to MCL (L-MCL), and compare them to a group of classic small-cell MCL (s-MCL) cases. Histologically, the MC origin of the large cells was evinced by their association with a small mantle cell component in the same tissue, or their distribution in a classic mantle zone pattern, or their development in a patient with previous s-MCL. The large cells were either pleomorphic mantle cells (case 1) or transformed blast-like cells (case 2-5). The median nuclear diameter, median nuclear area and proliferation index of L-MCLs and s-MCLs, were statistically different. Immunophenotypic characterization of four specimens of L-MCL and 10 of s-MCLs with a large panel of antibodies showed the classic findings of MCL, i.e. the IgM+ D+/-, CD5+, CD10-, CD23- phenotype in all cases except two (one CD5- and one CD23+), and the association with a loose follicular dendritic cell network. Two of four L-MCLs and 5/10 s-MCLs demonstrated rearrangements of the bcl-1 gene by Southern blot or by polymerase chain reaction (PCR); 2/4 L-MCLs and 1/9 s-MCLs had p53 mutations on single-strand conformation polymorphism analysis; none of the 14 specimens showed rearrangement of bcl-2 by PCR or bcl-6 and c-myc by Southern blot. All patients with 'transformed' histology (versus 37% of all others) died of lymphoma; their survival (15-18 months; median 17) was much shorter than that of all the others (28-117+ months; median 43) (P=0.0035). All three patients with p53 anomalies, two of whom had tumours with transformed histology, died of their disease in a short time (15, 18 and 28 months). In contrast, the presence of bcl-1 rearrangements did not have prognostic implications. This study documents the existence of large-cell variants of MCL and the poor prognosis associated with the 'transformed' cytologic type and/or p53 abnormalities.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0007-1048
pubmed:author
pubmed:issnType
Print
pubmed:volume
93
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
475-86
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:8639452-Aged, pubmed-meshheading:8639452-Base Sequence, pubmed-meshheading:8639452-Blotting, Southern, pubmed-meshheading:8639452-Cell Transformation, Neoplastic, pubmed-meshheading:8639452-Female, pubmed-meshheading:8639452-Gene Rearrangement, B-Lymphocyte, Heavy Chain, pubmed-meshheading:8639452-Humans, pubmed-meshheading:8639452-Immunohistochemistry, pubmed-meshheading:8639452-Lymphoma, Large B-Cell, Diffuse, pubmed-meshheading:8639452-Lymphoma, Non-Hodgkin, pubmed-meshheading:8639452-Male, pubmed-meshheading:8639452-Middle Aged, pubmed-meshheading:8639452-Molecular Sequence Data, pubmed-meshheading:8639452-Neoplasm Staging, pubmed-meshheading:8639452-Polymerase Chain Reaction, pubmed-meshheading:8639452-Prognosis, pubmed-meshheading:8639452-Retrospective Studies, pubmed-meshheading:8639452-Tumor Suppressor Protein p53
pubmed:year
1996
pubmed:articleTitle
Large-cell variants of mantle cell lymphoma: cytologic characteristics and p53 anomalies may predict poor outcome.
pubmed:affiliation
Department of Pathology, Division of Hematopathology/Molecular Pathology, New York University Medical Center, NY, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.