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

IF 3.9 2区 医学 Q2 CELL BIOLOGY Histopathology Pub Date : 2024-06-18 DOI:10.1111/his.15246
Ahmed Kazmi, Teo Feuerhake, Anoud Zidan, John Frewen, Andrew Carmichael, Janet Ross, Catherine H Orteu, Eduardo Calonje
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Abstract

Aims

There 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 results

Four 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.

Conclusion

Early 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.

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在组织病理学上表现为真菌病的变形病:四例说明性系列病例。
目的:有特例报告称,变形病的表皮病变与真菌病型(MF)皮肤 T 细胞淋巴瘤的组织病理重叠。这种现象在临床病理学上造成了一种模糊的情况,区分这些病症可能具有挑战性。本研究旨在通过一个病例系列来描述这种现象的临床、组织病理学和分子研究结果:方法:本研究发现了四名临床表现为典型的变形病,但组织病理学表现不寻常的患者,他们的组织病理学表现为典型的变形病,同时表皮内的 CD8 阳性淋巴细胞与 MF 无法区分。变形病的临床表型多种多样,均出现在疾病活动期的早期。它们都表现为表皮内淋巴细胞标记和细胞学不典型性。还可见保特里尔样微脓肿。通过分子分析,两个病例出现克隆性 TCR 基因重排。所有病例的随访结果均与典型形态病一致:结论:早期变形病很少出现非典型克隆性表皮内淋巴细胞,与 MF 无异。这些变化可发生在几种不同临床亚型的变形病中,这一事实提出了一种可能性,即早期疾病的炎症模式可能比目前所认识到的更为常见。
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来源期刊
Histopathology
Histopathology 医学-病理学
CiteScore
10.20
自引率
4.70%
发文量
239
审稿时长
1 months
期刊介绍: Histopathology is an international journal intended to be of practical value to surgical and diagnostic histopathologists, and to investigators of human disease who employ histopathological methods. Our primary purpose is to publish advances in pathology, in particular those applicable to clinical practice and contributing to the better understanding of human disease.
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