Diagnostic Challenges of Early Mycosis Fungoides in Skin of Color: A Case Report and Review

Mycosis fungoides (MF), the most common type of primary cutaneous T-cell lymphoma, presents a formidable diagnostic challenge, particularly in its early stages and in patients with darker skin tones. The initial lesion in this case was diagnosed as cellulitis, a common bacterial skin infection, despite the absence of significant pain, a less typical but documented presentation of cellulitis, which can also manifest as burning, itching, or mere redness and swelling without pronounced tenderness. This case report details the diagnostic journey from initial misdiagnosis to eventual identification of MF in a 57-year-old woman. The report emphasizes the overlapping clinical and histopathological features between MF and more prevalent inflammatory dermatoses, which often lead to diagnostic delays. By including a detailed timeline, comprehensive patient history, explicit diagnostic reasoning, and informed consent declaration, this report aims to highlight the unique barriers to MF diagnosis, especially in individuals with darker skin, and to provide practical insights for clinicians navigating similar diagnostic dilemmas. The rarity and subtlety of early MF, compounded by its ability to mimic benign conditions such as eczema, psoriasis, and cellulitis, underscore the need for heightened clinical suspicion and multidisciplinary collaboration in dermatologic practice.

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Publication Details

Journal
Cureus
Published
2025-04-27
DOI
https://doi.org/10.7759/cureus.83081
Primary Topic
Cutaneous lymphoproliferative disorders research
Type
article
Field-Weighted Citation Impact
0.00
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article

Diagnostic Challenges of Early Mycosis Fungoides in Skin of Color: A Case Report and Review

Pádraig Daly, Patricia Wessler
Cureus
Cutaneous lymphoproliferative disorders research
article

Diagnostic Challenges of Early Mycosis Fungoides in Skin of Color: A Case Report and Review

Pádraig Daly, Patricia Wessler
article en

Abstract

Mycosis fungoides (MF), the most common type of primary cutaneous T-cell lymphoma, presents a formidable diagnostic challenge, particularly in its early stages and in patients with darker skin tones. The initial lesion in this case was diagnosed as cellulitis, a common bacterial skin infection, despite the absence of significant pain, a less typical but documented presentation of cellulitis, which can also manifest as burning, itching, or mere redness and swelling without pronounced tenderness. This case report details the diagnostic journey from initial misdiagnosis to eventual identification of MF in a 57-year-old woman. The report emphasizes the overlapping clinical and histopathological features between MF and more prevalent inflammatory dermatoses, which often lead to diagnostic delays. By including a detailed timeline, comprehensive patient history, explicit diagnostic reasoning, and informed consent declaration, this report aims to highlight the unique barriers to MF diagnosis, especially in individuals with darker skin, and to provide practical insights for clinicians navigating similar diagnostic dilemmas. The rarity and subtlety of early MF, compounded by its ability to mimic benign conditions such as eczema, psoriasis, and cellulitis, underscore the need for heightened clinical suspicion and multidisciplinary collaboration in dermatologic practice.

CureusVol. 17(4)
Riverside Regional Medical Center (US), Edward Via College of Osteopathic Medicine (US)
Zero hunger
Openalex Percentile: Top 83%
Cutaneous lymphoproliferative disorders research
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