TY - JOUR
T1 - Late-delayed cerebral involvement in systemic non-hodgkin lymphoma
T2 - A second primary tumor or a tardy recurrence?
AU - Lossos, Alexander
AU - Ashhab, Yaqoub
AU - Sverdlin, Elena
AU - Amir, Gail
AU - Ben-Yehuda, Dina
AU - Siegal, Tali
PY - 2004/10/15
Y1 - 2004/10/15
N2 - BACKGROUND. Central nervous system involvement is a well recognized complication of systemic non-Hodgkin lymphoma. Most central nervous system recurrences occur within the first 2 years after the initial diagnosis and are considered to represent clonally related recurrence of systemic disease. The authors attempted to investigate the clonal relation between the late-delayed central nervous system involvement and the original systemic tumor. METHODS. The authors studied archival, formalin fixed, paraffin embedded tissue samples from 8 patients with isolated cerebral involvement diagnosed > 3 years after their initial presentation with aggressive, systemic, B-cell non-Hodgkin lymphoma. The rearranged immunoglobulin heavy-chain variable region genes (VH) from both sites were amplified by polymerase chain reaction and were sequenced when necessary. RESULTS. In three of five patients who had interpretable results, a distinct, monoclonal, VH family-specific band profile was obtained from the cerebral and systemic lymphoma. In the other two patients, a similar VH band pattern was observed and also was compared using direct sequencing, which demonstrated sequence differences between tumors from the two sites. CONCLUSIONS. Clonal variance between the cerebral and systemic lymphoma in these patients suggested the possibility that some instances of late-delayed recurrence in the central nervous system represent a second, new B-cell lymphoma rather than a true recurrence of the original systemic tumor, a finding that may have significant clinical and biologic implications.
AB - BACKGROUND. Central nervous system involvement is a well recognized complication of systemic non-Hodgkin lymphoma. Most central nervous system recurrences occur within the first 2 years after the initial diagnosis and are considered to represent clonally related recurrence of systemic disease. The authors attempted to investigate the clonal relation between the late-delayed central nervous system involvement and the original systemic tumor. METHODS. The authors studied archival, formalin fixed, paraffin embedded tissue samples from 8 patients with isolated cerebral involvement diagnosed > 3 years after their initial presentation with aggressive, systemic, B-cell non-Hodgkin lymphoma. The rearranged immunoglobulin heavy-chain variable region genes (VH) from both sites were amplified by polymerase chain reaction and were sequenced when necessary. RESULTS. In three of five patients who had interpretable results, a distinct, monoclonal, VH family-specific band profile was obtained from the cerebral and systemic lymphoma. In the other two patients, a similar VH band pattern was observed and also was compared using direct sequencing, which demonstrated sequence differences between tumors from the two sites. CONCLUSIONS. Clonal variance between the cerebral and systemic lymphoma in these patients suggested the possibility that some instances of late-delayed recurrence in the central nervous system represent a second, new B-cell lymphoma rather than a true recurrence of the original systemic tumor, a finding that may have significant clinical and biologic implications.
KW - Central nervous system
KW - Clonality
KW - Gene rearrangement
KW - Non-Hodgkin lymphoma
KW - Recurrence
UR - http://www.scopus.com/inward/record.url?scp=4744358775&partnerID=8YFLogxK
U2 - 10.1002/cncr.20575
DO - 10.1002/cncr.20575
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 15372481
AN - SCOPUS:4744358775
SN - 0008-543X
VL - 101
SP - 1843
EP - 1849
JO - Cancer
JF - Cancer
IS - 8
ER -