A Rare Case of Primary Cutaneous Epstein-Barr Virus-Positive T Follicular Helper Cell Lymphoma

We herein report a case of Epstein-Barr virus-positive primary cutaneous T follicular helper cell lymphoma (EBV-positive pcTFHL) in an elderly patient. The patient presented with multiple erythemas and cutaneous and subcutaneous nodules on the legs without internal organ involvement. Histology demonstrated diffuse infiltrates of atypical small- to medium-sized lymphoid cells in the dermis and subcutis associated with exocytosis in the epidermis and extensive necrosis in the deep dermis. Immunohistochemistry demonstrated that the atypical lymphoid cells were CD3- and CD4-positive T cells and expressed TFH cell markers. The CD4-positive atypical lymphoid cells were also diffusely positive for EBV byin situ hybridization, confirming the diagnosis of EBV-positive pcTFHL. The clinical course was progressive: large multiple cutaneous ulcers developed, and the patient died of fibrinous and organizing pneumonia due to COVID-19. The total clinical course was two years and two months after the onset of the skin rashes. This is the third case of EBV-positive pcTFHL that showed EBV infection exclusively in CD3- and CD4-positive T cells and had a lethal progressive clinical course.

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Publication Details

Journal
Cureus
Published
2025-11-15
DOI
https://doi.org/10.7759/cureus.96925
Primary Topic
Cutaneous lymphoproliferative disorders research
Type
article
Field-Weighted Citation Impact
0.00

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article

A Rare Case of Primary Cutaneous Epstein-Barr Virus-Positive T Follicular Helper Cell Lymphoma

Morishige Takeshita, Yuzo Oyama, Osamu Okamoto, Rika Maruyama et al.
Cureus
Cutaneous lymphoproliferative disorders research
article

A Rare Case of Primary Cutaneous Epstein-Barr Virus-Positive T Follicular Helper Cell Lymphoma

Morishige Takeshita, Yuzo Oyama, Osamu Okamoto, Rika Maruyama, Kentaro Nagamatsu
article en

Abstract

We herein report a case of Epstein-Barr virus-positive primary cutaneous T follicular helper cell lymphoma (EBV-positive pcTFHL) in an elderly patient. The patient presented with multiple erythemas and cutaneous and subcutaneous nodules on the legs without internal organ involvement. Histology demonstrated diffuse infiltrates of atypical small- to medium-sized lymphoid cells in the dermis and subcutis associated with exocytosis in the epidermis and extensive necrosis in the deep dermis. Immunohistochemistry demonstrated that the atypical lymphoid cells were CD3- and CD4-positive T cells and expressed TFH cell markers. The CD4-positive atypical lymphoid cells were also diffusely positive for EBV byin situ hybridization, confirming the diagnosis of EBV-positive pcTFHL. The clinical course was progressive: large multiple cutaneous ulcers developed, and the patient died of fibrinous and organizing pneumonia due to COVID-19. The total clinical course was two years and two months after the onset of the skin rashes. This is the third case of EBV-positive pcTFHL that showed EBV infection exclusively in CD3- and CD4-positive T cells and had a lethal progressive clinical course.

CureusVol. 17(11)
Oita University (JP), Almeida Memorial Hospital (JP), Saiseikai Yahata General Hospital (JP)
Fukuoka University
Openalex Percentile: Top 43%
Cutaneous lymphoproliferative disorders research
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A Rare Case of Primary Cutaneous Epstein-Barr Virus-Positive T Follicular Helper Cell Lymphoma — Morishige Takeshita, Yuzo Oyama, et al. · Cureus (2025) | TGRS Research Map | TGRS