This overview of the fifth edition of the WHO classification of thymic epithelial tumors
(including thymomas, thymic carcinomas, and thymic neuroendocrine tumors [NETs]) …

Soft tissue tumors are a relatively rare and diagnostically challenging group of neoplasms
that can have varying lines of differentiation. Accurate diagnosis is important for appropriate …

The fifth edition of the World Health Organization Classification of Tumors of Soft Tissue and
Bone was published in early 2020. The revisions reflect a consensus among an …

Solitary fibrous tumors are an uncommon sarcoma type characterized by NAB2–STAT6
gene fusion. While solitary fibrous tumors metastasize in 5–25% of cases, it has historically …

Solitary fibrous tumor (SFT) is composed of spindled to ovoid cells in a patternless
architecture with prominent stromal collagen and hemangiopericytoma-like vessels. Some …

Abstract Background Solitary Fibrous Tumor (SFT) is a distinct soft tissue neoplasm
associated with NAB2-STAT6 gene fusion. It can involve a number of anatomic sites and …

Simple Summary Solitary fibrous tumor (SFT) is a malignant condition that exhibits different
clinical behaviors ranging from low to high aggressive SFT, with dedifferentiated SFT (DD …

Solitary fibrous tumor (SFT) is an uncommon fibroblastic neoplasm. Although histologic
characteristics and frequent CD34 expression allow for an accurate diagnosis in the majority …

Solitary fibrous tumor (SFT) is a rare tumor of mesenchymal origin that account for less than
2% of all soft tissue masses. Initially identified in the pleura, SFT has been identified in …

Solitary fibrous tumor of the pleura is a mesenchymal tumor that has been increasingly
recognized over the past few years. The tumor was initially described in the pleura, but it has …