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Updated: Jan 25, 2026

A Melanoma Patient-Derived Xenograft Model
Published on: May 20, 2019
Detection of a new melanoma in a patient treated with fingolimod
Yves Michiels1, Olivier Bugnon1,2, Jean-François Michiels3
1Center for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland.
Abstract:
In addition to the TRANSFORMS, FREEDOMS, INFORMS studies, very few publications have identified new cases of skin cancer in patients treated with fingolimod. Here, we present the case of a 52-year-old Caucasian patient with relapsing remitting multiple sclerosis for 19 years, with a phototype II with blue eyes, light brown hair, no personal or family history of melanoma and a low number of naevi (<10). She did not experience intense sun exposure in childhood as well as severe sunburn and did not practise sessions in ultraviolet cabins. This case is distinguished from other published cases, usually superficial spreading malignant melanoma by its unclassifiable histological character. The occurrence of skin cancers in patients with multiple sclerosis remains exceptional, but new cases have recently emerged requiring the strengthening of dermatological follow-up of such patients.
Insights
Skin cancer is rare in multiple sclerosis patients on fingolimod. This case highlights an unusual melanoma, emphasizing the need for enhanced dermatological monitoring in these individuals.
Area of Science:
- Dermatology
- Neurology
- Oncology
Background:
- Fingolimod is a disease-modifying therapy for relapsing remitting multiple sclerosis.
- Previous studies (TRANSFORMS, FREEDOMS, INFORMS) have rarely reported skin cancer in patients using fingolimod.
- Skin cancers, particularly melanoma, are infrequently observed in multiple sclerosis patients.
Observation:
- A 52-year-old Caucasian female with a 19-year history of relapsing remitting multiple sclerosis was diagnosed with skin cancer.
- The patient had phototype II, no significant history of sun exposure, sunburns, or UV cabin use, and few nevi.
- The diagnosed skin cancer presented with unclassifiable histological characteristics, distinguishing it from typical superficial spreading malignant melanoma.
Findings:
- This case presents a rare instance of unclassifiable skin cancer in a multiple sclerosis patient treated with fingolimod.
- The histological features of this melanoma were atypical compared to previously reported cases.
- The occurrence of skin cancers in multiple sclerosis patients, while exceptional, is an emerging concern.
Implications:
- The findings suggest a potential need for increased vigilance regarding skin cancer development in multiple sclerosis patients.
- Enhanced dermatological surveillance is recommended for patients undergoing treatment with fingolimod.
- Further research is warranted to understand the risk factors and specific types of skin cancers associated with fingolimod therapy.
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