Plexiformer fibrohistiozytärer Tumor View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-11

AUTHORS

L. Pissoat, M. Megahed

ABSTRACT

Plexiform fibrohistiocytic tumor is a rare soft-tissue tumor with intermediate malignancy. It has a predilection for girls and young women. A 6-year-old girl presented with an indolent nodule in the right axilla first noticed six months earlier. Clinical and histopathological criteria led to the diagnosis plexiform fibrohistiocytic tumor. As relapses may occur and some cases of metastasis have been reported, lesions should be excised. Long-term follow-up is required to promptly identify any local recurrence as well as nodal and pulmonary metastases. More... »

PAGES

809-812

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00105-011-2246-2

DOI

http://dx.doi.org/10.1007/s00105-011-2246-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1029688924

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/22037884


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