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 …

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

Objective: To assess tumor behavior and the efficacy of active surveillance (AS) in patients
with desmoid-type fibromatosis (DTF). Summary of Background Data: AS is recommended …

Solitary fibrous tumors (SFTs) are rare fibroblastic mesenchymal tumors that are usually
benign with variable malignant potential. They can develop in any organ due to their spindle …

Desmoid tumors (DT) are rare, slow-growing, locally invasive soft tissue tumors that often
pose significant therapeutic challenges. Traditional management strategies including active …

Desmoid tumors (DTs) are a rare and biologically heterogeneous group of locally
aggressive fibroblastic neoplasm: their biological behavior spectrum ranges from indolent to …

Desmoid-type fibromatosis (DF) is a soft tissue tumor characterized by infiltrative growth and
a tendency toward local recurrence, while it exhibits self-limiting behavior and shows …

OBJECTIVE. The response of desmoid tumors (DTs) to chemotherapy is evaluated with
Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) in daily practice and …

Opinion statement Desmoid tumors are rare tumors with a tendency to infiltrate locally. The
lack of a standard treatment approach makes choosing the most appropriate treatment for …

Fibroblastic and myofibroblastic tumors are a variable group of neoplasms ranging from
benign to malignant. These lesions may affect patients of any age group but are more …