4.1 Article

Epidermotropic secondary cutaneous involvement by relapsed angioimmunoblastic T-cell lymphoma mimicking mycosis fungoides: a case report

Journal

JOURNAL OF CUTANEOUS PATHOLOGY
Volume 39, Issue 12, Pages 1119-1124

Publisher

WILEY-BLACKWELL
DOI: 10.1111/cup.12022

Keywords

angio-immunoblastic T-cell lymphoma; CXCL13; epidermotropism; mycosis fungoides; PD1

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Angioimmunoblastic T-cell lymphoma (AITL) is frequently associated with skin lesions, but epidermotropic cutaneous involvement has never been described. A 37-year-old man presented with erythematous and pruriginous plaques, clinically suggestive of mycosis fungoides, distributed all over the body, 3?weeks after the last line of a polychemotherapy, given for an AITL diagnosed 1?year earlier on a lymph node biopsy. Skin biopsy showed an epidermotropic CD4+ T-cell lymphoma, so that a diagnosis of mycosis fungoides was first proposed. Further investigations showed that atypical lymphocytes strongly expressed CD10 and markers of follicular helper T cells (TFH) including PD1, BCL-6 and CXCL13. The diagnosis of an unusual epidermotropic cutaneous localization of the AITL was finally made, supported by the presence of the same T-cell clone in the initial lymph node biopsy and the skin. We therefore recommend performing markers of TFH cells in patients with unusual epidermotropic cutaneous T-cell lymphomas, particularly if they have any clinical features suggestive of AITL.

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