Intravascular large T-cell lymphoma : a case report of CD30-positive and ALK-negative anaplastic type with cytotoxic molecule expression

We reported a case of intravascular T-cell lymphoma (T-IVL) with anaplastic large cell morphology, the hemophagocytic syndrome, and an aggressive clinical course. Phenotypic analysis of the tumor cells revealed CD2+, CD3-, CD4+, CD5-, CD8-, CD30+, CD56-, T-cell receptor alpha/beta-, ALK-, TIA1+, gra...

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Veröffentlicht in:Virchows Archiv : an international journal of pathology 2005-12, Vol.447 (6), p.1000-1006
Hauptverfasser: TAKAHASHI, Emiko, KAJIMOTO, Kazuyoshi, FUKATSU, Toshiaki, YOSHIDA, Megumi, EIMOTO, Tadaaki, NAKAMURA, Shigeo
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Sprache:eng
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Zusammenfassung:We reported a case of intravascular T-cell lymphoma (T-IVL) with anaplastic large cell morphology, the hemophagocytic syndrome, and an aggressive clinical course. Phenotypic analysis of the tumor cells revealed CD2+, CD3-, CD4+, CD5-, CD8-, CD30+, CD56-, T-cell receptor alpha/beta-, ALK-, TIA1+, granzyme B+, and perforin+. No association with Epstein-Barr virus was found by in situ hybridization. A review revealed that 25 cases of T-IVL have been reported in the available literature, only two of which were of CD30+ anaplastic large cell or cytotoxic T-cell type. The findings in the present case may highlight the unique clinicopathologic aspects of a subset of CD30-positive T-IVLs with an ALK-negative cytotoxic phenotype.
ISSN:0945-6317
1432-2307
DOI:10.1007/s00428-005-0080-6