KURODA Hajime
Department School of Medicine(Tokyo Women's Medical University Adachi Medical Center), School of Medicine Position Professor |
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Article types | Original article |
Language | English |
Peer review | Peer reviewed |
Title | No evidence of a correlation between BCL10 expression and API2-MALT1 gene rearrangement in ocular adnexal MALT lymphoma. |
Journal | Formal name:Pathology international Abbreviation:Pathol Int ISSN code:14401827/13205463 |
Domestic / Foregin | Foregin |
Volume, Issue, Page | 54(1),pp.16-25 |
Author and coauthor | Adachi Akiko, Tamaru Jun-ichi, Kaneko Kou, Kuroda Hajime, Miura Ichiro, Kojima Takayoshi, Hoshino Shigeru, Ichinohasama Ryo, Itoyama Shinji |
Publication date | 2004/01 |
Summary | In the present study, 62 cases of ocular adnexal lymphoproliferative disorders were reviewed clinicopathologically. Of them, 51 were extranodal marginal zone B-cell lymphoma (MALT lymphoma), five were diffuse large B-cell lymphoma (DLBCL), one was peripheral T-cell lymphoma, one was NK/T cell lymphoma, nasal type, and four were reactive lymphoid hyperplasia. These lymphoma cases showed a favorable clinical course and localized disease, except for the case of NK/T cell lymphoma, although 19 cases (32.8%) had a recurrence of disease. To clarify the correlation between BCL10 protein expression and API2-MALT1 gene rearrangement, the 51 cases of MALT lymphoma and 5 cases of DLBCL were analyzed by immunohistochemical and RT-PCR methods. Nuclear BCL10 expression was identified in 58% of MALT lymphoma cases, but not in any DLBCL cases. There was no evidence of a correlation between aberrant nuclear BCL10 expression and the clinical parameters examined in the present study. API2-MALT1 transcription was not demonstrated in either the MALT lymphoma cases or the DLBCL cases studied using a multiplex one-tube reverse transcriptase-PCR method. These findings indicate that the nuclear expression of BCL10 is unlikely to correlate with the API2-MALT1 fusion gene in ocular adnexal MALT lymphoma. |
DOI | 10.1111/j.1440-1827.2004.01580.x |
PMID | 14674990 |