Soft‐tissue sarcomas (STS) are rare tumors that account for 1% of all adult malignancies,
with over 100 different histologic subtypes occurring predominately in the trunk, extremity …

Desmoid-type fibromatosis is a rare and locally aggressive monoclonal, fibroblastic
proliferation characterized by a variable and often unpredictable clinical course. Currently …

Soft tissue sarcomas (STS) are rare tumours arising in mesenchymal tissues, and can occur
almost anywhere in the body. Their rarity, and the heterogeneity of subtype and location …

The management of desmoid tumors requires multidisciplinary expertise by an experienced
team. We must fully understand the physiopathology of the disease (factors influencing the …

Desmoid-type fibromatosis (DF) is a rare monoclonal, fibroblastic proliferation characterised
by a variable and often unpredictable clinical course. It may affect nearly all parts of the body …

Desmoid tumors (DTs) are rare soft tissue mesenchymal neoplasms that may be associated
with impairments, disfigurement, morbidity, and (rarely) mortality. DT disease course can be …

Background To analyse the natural history of extra-abdominal wall desmoid-type
fibromatosis (DF) and compare outcome in patients who underwent initial surgery with those …

Desmoid-type fibromatosis (DF) is a locally aggressive fibroblastic neoplasm that has
variable clinical and biologic behaviors ranging from indolent tumors that can undergo …

Objective The purpose of this article is to review the etiopathogenesis, molecular
cytogenetics, histopathology, clinical features, and multimodality imaging features of …

Background Extra-abdominal desmoid-type fibromatosis (DF) is a rare, locally aggressive
neoplasm that is usually managed conservatively. When treatment is indicated, it typically …