CD30+ clonal T-cell lymphoid proliferation of the skin in a patient with hypereosinophilic syndrome.

Abstract:

:We report a hitherto undescribed unusual CD30+ clonal T-cell proliferation in a 46-year-old man with the lymphocytic variant of hypereosinophilic syndrome with a 17-year history of pruritus, generalized persistent papulonodular skin lesions and peripheral blood hypereosinophilia. A skin biopsy showed an eosinophil-rich infiltrate with small to medium-sized CD30+ lymphocytes and Churg-Strauss granulomas. Peripheral blood flow cytometry revealed an aberrant T-cell clone which, molecular genetically, was identical to the T-cell clone detected in the skin. No genetic aberrations of platelet-derived growth factor receptor alpha (PDGFRA), FIP1L1-PDGFRA, PDGFRB or FGFR1 were found. The skin lesions showed transient response to systemic and topical corticosteroids. The skin lesions represent cutaneous involvement by clonal T-cells in hypereosinophilic syndrome and differ from known cutaneous CD30+ lymphoproliferative disorders.

journal_name

J Cutan Pathol

authors

Kempf W,Kazakov DV,Szep Z,Vanecek T

doi

10.1111/cup.12454

subject

Has Abstract

pub_date

2015-02-01 00:00:00

pages

130-5

issue

2

eissn

0303-6987

issn

1600-0560

journal_volume

42

pub_type

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