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- Publisher Website: 10.1309/E5PR-6A9R-Q02N-8QVW
- Scopus: eid_2-s2.0-0035126174
- PMID: 11211616
- WOS: WOS:000166658500014
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Article: Bone marrow involvement by nasal NK cell lymphoma at diagnosis is uncommon
Title | Bone marrow involvement by nasal NK cell lymphoma at diagnosis is uncommon |
---|---|
Authors | |
Keywords | Bone marrow CD56 EBV EBV-encoded early RNA Epstein-Barr virus In situ hybridization Nasal lymphoma Nasopharyngeal lymphoma Natural killer cell NK cell lymphoma |
Issue Date | 2001 |
Publisher | American Society for Clinical Pathology. The Journal's web site is located at http://www.ajcp.com |
Citation | American Journal Of Clinical Pathology, 2001, v. 115 n. 2, p. 266-270 How to Cite? |
Abstract | To look for subtle evidence of marrow involvement in nasal NK cell lymphoma at diagnosis, we retrospectively studied trephine biopsy specimens from 25 consecutive patients by 2 sensitive techniques: CD56 immunohistochemistry and Epstein-Barr virus-encoded RNA in situ hybridization (EBER ISH). Only 2 patients had marrow involvement by NK cell lymphoma at diagnosis. In 3 additional patients, marrow involvement developed during or after systemic recurrence. All 5 positive cases were revealed by EBER ISH, but only 3 cases showed CD56 immunoreactivity. Among the 5 cases, only 2 were recognized by morphologic assessment. All 5 patients died, often within a short period, compared with a mortality of 50% for patients without demonstrable marrow involvement. Marrow involvement is distinctly uncommon in nasal NK cell lymphoma at diagnosis, and EBER ISH is the most sensitive technique for the demonstration of occult NK cell lymphoma. Despite the low frequency of marrow involvement in nasal NK cell lymphoma, EBER ISH is worthwhile to identify the minor subgroup of patients with a high likelihood of early death due to disease and when autologous bone marrow or peripheral blood stem cell transplantation is contemplated. |
Persistent Identifier | http://hdl.handle.net/10722/148237 |
ISSN | 2023 Impact Factor: 2.3 2023 SCImago Journal Rankings: 0.775 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wong, KF | en_US |
dc.contributor.author | Chan, JKC | en_US |
dc.contributor.author | Cheung, MMC | en_US |
dc.contributor.author | So, JCC | en_US |
dc.date.accessioned | 2012-05-29T06:11:42Z | - |
dc.date.available | 2012-05-29T06:11:42Z | - |
dc.date.issued | 2001 | en_US |
dc.identifier.citation | American Journal Of Clinical Pathology, 2001, v. 115 n. 2, p. 266-270 | en_US |
dc.identifier.issn | 0002-9173 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/148237 | - |
dc.description.abstract | To look for subtle evidence of marrow involvement in nasal NK cell lymphoma at diagnosis, we retrospectively studied trephine biopsy specimens from 25 consecutive patients by 2 sensitive techniques: CD56 immunohistochemistry and Epstein-Barr virus-encoded RNA in situ hybridization (EBER ISH). Only 2 patients had marrow involvement by NK cell lymphoma at diagnosis. In 3 additional patients, marrow involvement developed during or after systemic recurrence. All 5 positive cases were revealed by EBER ISH, but only 3 cases showed CD56 immunoreactivity. Among the 5 cases, only 2 were recognized by morphologic assessment. All 5 patients died, often within a short period, compared with a mortality of 50% for patients without demonstrable marrow involvement. Marrow involvement is distinctly uncommon in nasal NK cell lymphoma at diagnosis, and EBER ISH is the most sensitive technique for the demonstration of occult NK cell lymphoma. Despite the low frequency of marrow involvement in nasal NK cell lymphoma, EBER ISH is worthwhile to identify the minor subgroup of patients with a high likelihood of early death due to disease and when autologous bone marrow or peripheral blood stem cell transplantation is contemplated. | en_US |
dc.language | eng | en_US |
dc.publisher | American Society for Clinical Pathology. The Journal's web site is located at http://www.ajcp.com | en_US |
dc.relation.ispartof | American Journal of Clinical Pathology | en_US |
dc.subject | Bone marrow | - |
dc.subject | CD56 | - |
dc.subject | EBV | - |
dc.subject | EBV-encoded early RNA | - |
dc.subject | Epstein-Barr virus | - |
dc.subject | In situ hybridization | - |
dc.subject | Nasal lymphoma | - |
dc.subject | Nasopharyngeal lymphoma | - |
dc.subject | Natural killer cell | - |
dc.subject | NK cell lymphoma | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Aged, 80 And Over | en_US |
dc.subject.mesh | Amsacrine - Administration & Dosage | en_US |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols - Administration & Dosage - Therapeutic Use | en_US |
dc.subject.mesh | Bleomycin - Administration & Dosage | en_US |
dc.subject.mesh | Bone Marrow - Chemistry - Pathology | en_US |
dc.subject.mesh | Chemotherapy, Adjuvant | en_US |
dc.subject.mesh | Cyclophosphamide - Administration & Dosage | en_US |
dc.subject.mesh | Cytarabine - Administration & Dosage | en_US |
dc.subject.mesh | Epirubicin - Administration & Dosage | en_US |
dc.subject.mesh | Etoposide - Administration & Dosage | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunoenzyme Techniques | en_US |
dc.subject.mesh | In Situ Hybridization | en_US |
dc.subject.mesh | Killer Cells, Natural - Chemistry - Pathology | en_US |
dc.subject.mesh | Lymphoma - Chemistry - Pathology - Therapy | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Methotrexate - Administration & Dosage | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Nose Neoplasms - Chemistry - Pathology - Therapy | en_US |
dc.subject.mesh | Prednisone - Administration & Dosage | en_US |
dc.subject.mesh | Rna, Viral - Analysis | en_US |
dc.subject.mesh | Radiotherapy | en_US |
dc.subject.mesh | Treatment Outcome | en_US |
dc.subject.mesh | Vincristine - Administration & Dosage | en_US |
dc.title | Bone marrow involvement by nasal NK cell lymphoma at diagnosis is uncommon | en_US |
dc.type | Article | en_US |
dc.identifier.email | So, JCC:scc@pathology.hku.hk | en_US |
dc.identifier.authority | So, JCC=rp00391 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1309/E5PR-6A9R-Q02N-8QVW | en_US |
dc.identifier.pmid | 11211616 | - |
dc.identifier.scopus | eid_2-s2.0-0035126174 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035126174&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 115 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.spage | 266 | en_US |
dc.identifier.epage | 270 | en_US |
dc.identifier.isi | WOS:000166658500014 | - |
dc.publisher.place | United States | en_US |
dc.identifier.issnl | 0002-9173 | - |