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Clinical relevance of three subtypes of primary sinonasal lymphoma characterized by immunophenotypic analysis

Authors
 Gwi Eon Kim  ;  Woong Sub Koom  ;  Joo Hang Kim  ;  Jae Kyung Roh  ;  Jee Sook Hahn  ;  Chang Ok Suh  ;  Chang Geol Lee  ;  Ki Chang Keum  ;  Sang-Wook Lee  ;  Woo-Ick Yang 
Citation
 HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, Vol.26(7) : 584-593, 2004 
Journal Title
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
ISSN
 1043-3074 
Issue Date
2004
MeSH
Adolescent ; Adult ; Aged ; Antigens, CD20/metabolism ; CD56 Antigen/metabolism ; Female ; Humans ; Immunophenotyping* ; Killer Cells, Natural ; Lymphoma, B-Cell/classification ; Lymphoma, B-Cell/metabolism* ; Lymphoma, B-Cell/mortality ; Lymphoma, B-Cell/therapy ; Lymphoma, T-Cell/classification ; Lymphoma, T-Cell/metabolism* ; Lymphoma, T-Cell/microbiology ; Lymphoma, T-Cell/mortality ; Lymphoma, T-Cell/therapy ; Male ; Middle Aged ; Paranasal Sinus Neoplasms/classification ; Paranasal Sinus Neoplasms/metabolism* ; Paranasal Sinus Neoplasms/mortality ; Paranasal Sinus Neoplasms/therapy ; Prognosis ; Retrospective Studies ; Survival Analysis ; Treatment Failure
Keywords
sinonasal lymphomas ; NK/T‐cell lymphomas ; immunophenotype ; prognostic factor
Abstract
BACKGROUND:
The purpose of this study was to investigate the clinical relevance of subtypes categorized by immunophenotypic analysis in primary sinonasal lymphomas.
METHODS:
Eighty patients with localized non-Hodgkin's lymphoma involving the nasal cavity and/or paranasal sinuses were divided into three subtypes on the basis of their immunohistochemical findings: (A) B-cell lymphoma (n = 19), (B) T-cell lymphoma (n = 27), and (C) natural killer (NK)/T-cell lymphoma (n = 34). The clinicopathologic profiles, immunophenotypic data, patterns of treatment failure, and survival data among the three patient groups were retrospectively compared.
RESULTS:
The nasal cavity was the predominant site of involvement in T-cell and NK/T-cell lymphoma, whereas sinus involvement without nasal disease was common in B-cell lymphoma. Systemic B symptoms were frequently observed in NK/T-cell lymphoma. Almost all patients with NK/T-cell lymphoma showed a strong association with the Epstein-Barr virus by in situ hybridization studies. Sixty-five patients (81%) patients achieved complete remission after initial treatment, but 36 (55%) of these subsequently experienced treatment failure. Although there were no significant differences in locoregional failure rates among the patients of the three groups, distant failure was far more common in B-cell or NK/T-cell lymphoma than in T-cell lymphoma (p =.005). Most B-cell lymphoma cases showed a predilection for sites of systemic failure in the nodal and extranodal sites below the diaphragm, such as the paraaortic lymph nodes or the gastrointestinal (GI) tract, whereas patients with NK/T-cell lymphoma showed an increased risk of systemic dissemination to the skin, testes, or GI tract, including the development of hemophagocytic syndrome. The 5-year actuarial and disease-free survival rates for all patients were 57% and 51%, respectively. Of the three subtypes of primary sinonasal lymphomas, T-cell lymphoma seemed to carry the most favorable prognosis and NK/T-cell lymphoma the worst. (The 5-year actuarial survival rate was 57% for B-cell lymphoma, 80% for T-cell lymphoma, 37% for NK/T-cell lymphoma; p =.02, log-rank.) By univariate and multivariate analyses, immunophenotype was identified as the most important prognostic factor.
CONCLUSIONS:
Our data indicate that the three subtypes of primary sinonasal lymphomas classified by immunohistochemical studies exhibit different clinical profiles, different patterns of failure, and different treatment outcomes. Given these observations, it is concluded that the recognition of these distinct subsets, diagnosed on the basis of immunophenotypic study, is very important and clinically relevant in predicting their potential behavior and prognosis.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/hed.20015/abstract
DOI
10.1002/hed.20015
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
Yonsei Authors
Keum, Ki Chang(금기창) ORCID logo https://orcid.org/0000-0003-4123-7998
Koom, Woong Sub(금웅섭) ORCID logo https://orcid.org/0000-0002-9435-7750
Kim, Gwi Eon(김귀언)
Kim, Joo Hang(김주항)
Roh, Jae Kyung(노재경)
Suh, Chang Ok(서창옥)
Yang, Woo Ick(양우익) ORCID logo https://orcid.org/0000-0002-6084-5019
Lee, Sang Wook(이상욱)
Lee, Chang Geol(이창걸) ORCID logo https://orcid.org/0000-0002-8702-881X
Hahn, Jee Sook(한지숙)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/111300
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