Results 41 to 50 of about 7,079 (165)
Desmoid tumors are rare, benign, fibromatous lesions that are the result of abnormal proliferation of myofibroblasts. Desmoid tumors can be classified as extra-abdominal and abdominal. Abdominal desmoid tumors are either superficial or intraabdominal.
Sakorafas, George H. +2 more
openaire +3 more sources
ABSTRACT Background PRRX1‐rearranged mesenchymal neoplasms are rare soft tissue tumors with a predilection for the superficial subcutaneous tissue. The PRRX1::KMT2D fusion variant is exceptionally rare, with only three previously reported cases, all of which were located in the intermuscular regions.
Weixiang Zhong, Yu Deng, Ke Sun
wiley +1 more source
Desmoid-type fibromatosis tumor in children: A narrative review of the literature
Desmoid tumors (DTs), or aggressive fibromatosis, are rare soft-tissue tumors known for their tendency to recur postsurgery. Originating in musculo-aponeurotic tissue, they can appear in various body locations.
Mohammed Awadh Bin-Salah +4 more
doaj +1 more source
Facial fibromatosis: benign and aggressive, yet treatable!
Fibromatosis or desmoid tumors are locally aggressive neoplasms that have a propensity for local invasion and recurrence. The mainstay of treatment is excision with negative margins and the role of radiotherapy is controversial.
Rodrigues Gabriel +5 more
doaj +1 more source
Fertility preservation in women with sarcoma: A real‐world experience
What's New? Sarcomas frequently affect adolescent girls and young women, but limited data exist on ovarian function following sarcoma treatment. This observational cohort study evaluated the feasibility, timing, and clinical relevance of fertility preservation in young women treated for high‐grade sarcomas or desmoid tumors.
Guillaume Beinse +11 more
wiley +1 more source
Unravelling the Mystery of Mesenteric Fibromatosis: A Rare Case Report
Mesenteric Fibromatosis (MF) is a proliferative fibroblastic lesion of the small intestinal mesentery. It constitutes 8% of all desmoid tumours, which represent 0.03% of all neoplasms.
Misha Shettigar +2 more
doaj +1 more source
ABSTRACT Radiomics, the practice of mining quantitative features from medical imaging, has gained increasing popularity in diagnosing and treating cancer. However, clinical deployment and adoption of radiomics tools in real‐world practice remain limited. To increase trust in radiomics models, one of the main remaining challenges is ensuring fairness by
Esmeralda Ruiz Pujadas +5 more
wiley +1 more source
Purpose: Desmoids are locally infiltrative, nonmalignant soft tissue tumors. Surgery, radiation therapy, and chemotherapy have been the mainstay of treatment, but relapse is common and side effects can result in significant morbidity.
Arash Najafi +2 more
doaj +1 more source
11‐year‐old girl presenting with blurred vision and progressive right arm weakness
Brain Pathology, EarlyView.
Trung Toan Tran +6 more
wiley +1 more source
ABSTRACT Introduction The management of extremity soft tissue sarcomas (STS) involving major vessels presents unique challenges, historically leading to amputation. Advances in vascular reconstruction have enabled limb‐sparing surgery (LSS), but outcomes and perioperative risks remain uncertain.
Lucas Monteiro Delgado +9 more
wiley +1 more source

