| Literature DB >> 19461249 |
Bruna Estrozi1, José A Sanches, Paulo C S Varela, Carlos E Bacchi.
Abstract
Mantle cell lymphoma (MCL) commonly involves extranodal sites, usually as a manifestation of disseminated disease. In rare cases, MCLs may arise as a primary tumor in the skin. Blastoid mantle cell lymphoma (BV-MCL) is a rare variant and has a more aggressive clinical course. The phenotype of BV-MCL is characterized as CD20+, CD5+, cyclin D1+, CD23-, and CD10-. Interphase fluorescence in situ hybridization shows a characteristic t(11;14) fusion pattern. We report a case of a BV-MCL arising in skin as primary cutaneous MCL with the characteristic immunophenotype and translocation.Entities:
Mesh:
Year: 2009 PMID: 19461249 DOI: 10.1097/DAD.0b013e31819d845a
Source DB: PubMed Journal: Am J Dermatopathol ISSN: 0193-1091 Impact factor: 1.533