par Goldschmidt, Denis 
;Raemdonck, D.;Verhest, Alain ;Noël, Jean Christophe ;Schuind, Frederic
Référence Annales de Chirurgie de la Main, 13, 1, page (46-48)
Publication Publié, 1994
;Raemdonck, D.;Verhest, Alain ;Noël, Jean Christophe ;Schuind, Frederic Référence Annales de Chirurgie de la Main, 13, 1, page (46-48)
Publication Publié, 1994
Article révisé par les pairs
| Résumé : | Plexiform fibrohistiocytic tumours are very rare, apparently benign neoplasms of the superficial soft tissue: only two series and one case report have been described in the literature. Macroscopically located within the dermis or superficial subcutis, they seem to predominate in the upper limbs of children and young adults. Moreover their reccurrence rate is relatively high. We report the case of a 56 year old male patient presenting such a plexiform fibrohistiocytic tumour of the hand, which was surgically excised after a progressive clinical evolution of approximately 5 years and in which no recurrence has been observed with a follow-up of more than 24 months. © 1994 Société d'Édition de l'Association d'Enseignement Médical des Hôpitaux de Paris. |
