Multiple Eruptive Dermatofibromas in a Patient with Myasthenia Gravis Treated with Systemic Corticosteroid / 대한피부과학회지
Korean Journal of Dermatology
; : 194-196, 2019.
Article
en Ko
| WPRIM
| ID: wpr-759712
Biblioteca responsable:
WPRO
ABSTRACT
Dermatofibroma is a fibrohistiocytic tumor of the skin that commonly occurs as a solitary lesion on the lower extremities of young women. Multiple eruptive dermatofibromas (MEDFs), defined as the presence of 5 to 8 dermatofibromas appearing within a period of 4 months, are rare, and the etiology of MEDFs remains unknown. However, MEDFs are frequently thought to be associated with altered immunity, such as autoimmune diseases and immunosuppression. It is unclear why MEDFs occur in association with these conditions, but this relationship may suggest that MEDFs are the result of an abortive immunoreactive process. We herein describe a middle-aged woman who developed multiple dermatofibroma. She had myasthenia gravis for 8 years, and developed MEDFs after undergoing oral corticosteroid treatment (245 mg/week) for 3 months. Therefore, our case suggests that the use of immunosuppressants is a more dominant factor for the development of MEDFs than underlying autoimmune diseases.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Piel
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Enfermedades Autoinmunes
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Terapia de Inmunosupresión
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Histiocitoma Fibroso Benigno
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Extremidad Inferior
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Inmunosupresores
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Miastenia Gravis
Límite:
Female
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Humans
Idioma:
Ko
Revista:
Korean Journal of Dermatology
Año:
2019
Tipo del documento:
Article