Morphoea presenting histopathologically as mycosis fungoides: an illustrative series of four cases

Author:

Kazmi Ahmed12,Feuerhake Teo3ORCID,Zidan Anoud3,Frewen John4,Carmichael Andrew5,Ross Janet6,Orteu Catherine H1,Calonje Eduardo3

Affiliation:

1. Royal Free London NHS Foundation Trust London UK

2. Sinclair Dermatology Melbourne Vic Australia

3. Guys & Thomas’ NHS Foundation Trust London UK

4. Royal Cornwall Hospitals NHS Trust Cornwall UK

5. James Cook University Hospital Middlesbrough UK

6. Lewisham University Hospital NHS Trust London UK

Abstract

AimsThere have been exceptional reports of morphoea presenting with epidermal changes overlapping histopathologically with cutaneous T cell lymphoma of the mycosis fungoides type (MF). This phenomenon gives rise to an ambiguous clinicopathological scenario in which distinguishing these conditions may be challenging. The aim of this study is to characterise the clinical, histopathological and molecular findings of this phenomenon through a case series.Methods and resultsFour patients with classical clinical presentation of morphoea but unusual histopathology displaying typical findings of morphoea, together with intra‐epidermal CD8 positive lymphocytes indistinguishable from MF, were identified. The clinical phenotypes of morphoea were varied, and they all presented early in the active phase of the disease. They all exhibited intra‐epidermal lymphocytes with tagging and cytological atypia. Pautrier‐like microabscesses were also seen. Using molecular analysis, two cases showed clonal TCR gene rearrangement. Follow‐up of all cases has been consistent with classical morphoea.ConclusionEarly morphoea can seldom present with atypical clonal intra‐epidermal lymphocytes indistinguishable from MF. The fact that these changes can occur in several different clinical subtypes of morphoea raises the possibility that this could be a pattern of inflammation in early disease more common than currently appreciated.

Publisher

Wiley

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