Follicular dendritic cell sarcoma (FDCS) is a rare neoplasm with a non-specific and insidious presentation further complicated by the difficult diagnostic and therapeutic assessment. It has a low to intermediate risk of recurrence and metastasis. Unlike other soft tissue sarcomas or histiocytic and dendritic cell neoplasms, cytogenetic studies are very limited in FDCS cases. Although no specific chromosomal marker has yet been established, complex aberrations and different ploidy types have been documented. We report the case of a 39-year-old woman with FDCS who presented to the Sultan Qaboos University Hospital in Muscat, Oman, in February 2013. Ultrastructural, immunophenotypical and histological findings are reported. In addition, karyotypic findings showed deletions of the chromosomes 1p, 3q, 6q, 7q, 8q and 11q. To the best of the authors' knowledge, these have not been reported previously in this tumour. Techniques such as spectral karyotyping may help to better characterise chromosomal abnormalities in this type of tumour.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554278PMC
http://dx.doi.org/10.18295/squmj.2015.15.03.017DOI Listing

Publication Analysis

Top Keywords

dendritic cell
12
follicular dendritic
8
cell sarcoma
8
sarcoma cytogenetics
4
cytogenetics pathological
4
pathological findings
4
findings follicular
4
sarcoma fdcs
4
fdcs rare
4
rare neoplasm
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!