Desmoid tumors (DT) are rare, locally aggressive, fibroblastic soft-tissue tumors that are
characterized by infiltrative growth and can affect organs and adjacent structures, resulting …

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 …

Sarcomas represent a distinct group of rare malignant tumors with high heterogeneity.
Limited options with clinical efficacy for the metastatic or local advanced sarcoma existed …

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

Soft tissue sarcomas (STS) have long been a formidable challenge in oncology, partly
because of their rarity and diversity, which complicates large-scale studies and slows the …

Purpose: Determine whether specific CTNNB1 or APC mutations in patients with desmoid
tumor were associated with differences in clinical responses to systemic treatments …

Desmoid tumor (DT) is a rare fibroblastic soft-tissue neoplasm that is characterized by local
aggressiveness but no metastatic potential. Although the prognosis is relatively favorable …

Desmoid tumours (DT) are rare locally infiltrative soft-tissue tumours which do not
metastasise. DT arise sporadically or are associated with familial syndromes, with different …

Background International chemoprevention preferences and approaches in Lynch
syndrome (LS) and APC-associated polyposis, including Familial adenomatous polyposis …

Mesentery was discovered as a new organ in 2017. It is a continuous membranous tissue
from the duodenojejunal flexure to the anorectal junction. It has distinct anatomy, physiology …