Literature DB >> 16115057

Plexiform fibrohistiocytic tumor: three unusual cases occurring in infancy.

Stéphanie Leclerc1, Dominique Hamel-Teillac, Patrice Oger, Nicole Brousse, Sylvie Fraitag.   

Abstract

BACKGROUND: Plexiform fibrohistiocytic tumor is a soft-tissue tumor of intermediate malignancy occurring in children and young adults but is only rarely found in infants. The tumor usually involves the upper limbs and is slow growing and painless. Recurrence rate is high. Lymph node and systemic metastases can occur, but have never been reported in infants. Clinical behavior in infancy is not known. Histologically, the tumor is characterized by nodules of histiocyte-like and multinucleated cells and fascicles of spindle cells arranged in a plexiform pattern. Mitosis, atypia, and nuclear pleomorphism are common but not pronounced. METHODS AND
RESULTS: We report three cases in infants, one of which is congenital, having an unusual topography and a broad histological spectrum.
CONCLUSION: In infants, wide excision with large safety margins should be performed as the behaviour of this tumor remains uncertain. Leclerc S, Hamel-Teillac D, Oger P, Brousse N, Fraitag S. Plexiform fibrohistiocytic tumor: three unusual cases occurring in infancy.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16115057     DOI: 10.1111/j.0303-6987.2005.00334.x

Source DB:  PubMed          Journal:  J Cutan Pathol        ISSN: 0303-6987            Impact factor:   1.587


  1 in total

1.  [Plexiform fibrohistiocytic tumor].

Authors:  L Pissoat; M Megahed
Journal:  Hautarzt       Date:  2011-11       Impact factor: 0.751

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.