Folliculotropic mycosis fungoides of the scalp: A case report

Folliculotropic Mycosis Fungoides (FMF) is a rare but distinct variant of mycosis fungoides, characterized by predominant follicular involvement and a typically more aggressive course. We report the case of a 65-year-old woman with a four-year history of scarring alopecia of the scalp associated with intense pruritus. Clinical and dermoscopic findings raised suspicion of a lymphoproliferative disorder. Histopathologic examination and immunohistochemistry confirmed the diagnosis of FMF (CD3+, CD4+, CD5+, CD7?, CD30?). FMF can mimic various dermatoses, leading to diagnostic delays. Management relies primarily on PUVA phototherapy, combined with systemic treatments. Early diagnosis is crucial due to the potentially aggressive behavior of this subtype.

Authors

Publication Details

Journal
Journal of Case Reports and Scientific Images
Published
2025-01-01
DOI
https://doi.org/10.22271/27080056.2025.v7.i1c.123
Primary Topic
Cutaneous lymphoproliferative disorders research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Folliculotropic mycosis fungoides of the scalp: A case report

Mariame Meziane, Laïla Benzekri, Zineb Loubaris, Ghita Filali Baba et al.
Journal of Case Reports and Scientific Images
Cutaneous lymphoproliferative disorders research
article

Folliculotropic mycosis fungoides of the scalp: A case report

Mariame Meziane, Laïla Benzekri, Zineb Loubaris, Ghita Filali Baba, Karima Senouc
article en

Abstract

Folliculotropic Mycosis Fungoides (FMF) is a rare but distinct variant of mycosis fungoides, characterized by predominant follicular involvement and a typically more aggressive course. We report the case of a 65-year-old woman with a four-year history of scarring alopecia of the scalp associated with intense pruritus. Clinical and dermoscopic findings raised suspicion of a lymphoproliferative disorder. Histopathologic examination and immunohistochemistry confirmed the diagnosis of FMF (CD3+, CD4+, CD5+, CD7?, CD30?). FMF can mimic various dermatoses, leading to diagnostic delays. Management relies primarily on PUVA phototherapy, combined with systemic treatments. Early diagnosis is crucial due to the potentially aggressive behavior of this subtype.

Journal of Case Reports and Scientific ImagesVol. 7(1)
Zero hunger
Openalex Percentile: Top 78%
Cutaneous lymphoproliferative disorders research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.