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滤泡树突细胞肉瘤：两个罕见的病例及对文献的简要回顾

 

Authors Ma Y, Sun JJ, Yang CC, Yuan DD, Liu J

Published Date July 2015 Volume 2015:8 Pages 1823—1830
DOI http://dx.doi.org/10.2147/OTT.S86502
Received 12 April 2015, Accepted 8 June 2015, Published 24 July 2015

Approved for publication by Professor Daniele Santini

 

Abstract: Follicular dendritic cell sarcoma (FDCS) is a rare malignant tumor recognized in recent years. It accounts for only 0.4% of soft-tissue sarcomas, and its underlying causes are largely unknown. A correct diagnosis can be difficult to make. Diagnosis of FDCS depends on the combined clinical examination, histopathologic features, electron microscopic examination and confirmation with immunohistochemical studies. Here, we report two rare cases of FDCS: one case involving multiple bones, and the other involving extensive
abdominal and pelvic cavities. Clinical, histopathological, and immunohistochemical aspects, therapeutic options, and a related literature review of the two cases are discussed. As the prevalence of FDCS is increasing, the details of these rare cases may highlight the importance and facilitate treatment of similar diseases.

Keywords: FDCS, bone, abdominal cavity, pelvic cavity, diagnosis, therapy


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