| Literature DB >> 10725869 |
B F Skinnider1, J M Connors, S B Sutcliffe, R D Gascoyne.
Abstract
The clinicopathologic features of anaplastic large cell lymphoma (ALCL) are reviewed. ALCL is a heterogeneous group of tumours, and histologic examination alone is not adequate in providing useful prognostic information. However, using a combination of clinical, phenotypic, and genotypic features, several distinct clinicopathologic entities have been identified. A subset of ALCL as presently defined is characterized by a balanced translocation, t(2;5)(p23;q35), resulting in a novel fusion protein (NPM-ALK) that can be readily detected by immunohistochemical methods using antibodies against the ALK protein. Detection of ALK protein, along with other methods for demonstrating the t(2;5), has assisted in identifying a distinct biologic entity within the heterogeneous group of ALCL with significant prognostic implications. It is important to separate these from cases of ALK-negative ALCL, which have a poorer prognosis, and cases of primary cutaneous ALCL, which have an excellent prognosis. Copyright 1999 John Wiley & Sons, Ltd.Entities:
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Year: 1999 PMID: 10725869 DOI: 10.1002/(sici)1099-1069(199912)17:4<137::aid-hon642>3.0.co;2-v
Source DB: PubMed Journal: Hematol Oncol ISSN: 0278-0232 Impact factor: 5.271