par Santos-Briz, Angel;García-Gavín, Juan;Pastushenko, Ievgenia
;Sayagués, José María;Rodríguez-Peralto, José Luis;Requena, Maria-Luisa Novella
Référence The American journal of dermatopathology, 42, 7, page (533-538)
Publication Publié, 2020-07-01

Référence The American journal of dermatopathology, 42, 7, page (533-538)
Publication Publié, 2020-07-01
Article révisé par les pairs
Résumé : | Dermatofibroma (DF) represents one of the most common mesenchymal proliferations of the skin. Their recurrence rate, even when incompletely excised, is very low, whereas the atypical, aneurysmal, and cellular variants have recurrence rates of up to 20% each. Extraordinary rare malignant lesions with metastases to lymph nodes and/or lung have been described. We report a 64-year-old woman with a long history (years) of a skin lesion on her right arm that became painful during the last months. Histologically, it consisted of a conventional cellular DF in which perineural invasion was present. Subsequently, the lesion showed a clinically aggressive course with recurrences, sarcomatous transformation, and pulmonary metastases. Given that no predictive morphological features have been identified to separate classical benign DF from rare metastasizing forms, perineural invasion in an otherwise conventional DF could be a histopathologic clue for an adverse prognosis and should provoke a closer clinical follow-up. |