Results 71 to 80 of about 13,029 (233)

Expanding the Anatomical Distribution of PRRX1::KMT2D Fusion Mesenchymal Neoplasms: A Rare Mediastinal Case Report

Cancer Reports, Volume 9, Issue 3, March 2026.
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

Molecular analysis of desmoid tumors with a high-density single-nucleotide polymorphism array identifies new molecular candidate lesions [PDF]

, 2012
Background: Desmoid tumors are neoplastic proliferations of connective tissues. The mutation status of the gene coding for catenin (cadherin-associated protein) beta 1 (CTNNB1) and trisomy 8 on the chromosomal level have been described to have prognostic
Erben, Philipp, Hofheinz, Ralf-Dieter, Hofmann, Wolf-Karsten, Hohenberger, Peter, Kasper, Bernd, Nowak, Daniel, Sauer, Christian, Ströbel, Philipp   +7 more
core   +1 more source

A Rapidly Growing Abdominal Mass: Desmoid Tumor in Pregnancy

American Journal of Perinatology Reports, 2015
Background Desmoid tumors are benign soft tissue tumors that locally invade adjacent tissue. There is a paucity of reports describing the rapid growth of these tumors during pregnancy.
Mateo G. Leon, Hind N. Moussa, Malahat Movahedian, Oscar A. Viteri, Monica Longo, Baha M. Sibai   +5 more
doaj   +1 more source

Fertility preservation in women with sarcoma: A real‐world experience

International Journal of Cancer, Volume 158, Issue 5, Page 1178-1183, 1 March 2026.
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, Pascaline Boudou‐Rouquette, Sixtine de Percin, Anne Fortin, Johanna Noel, Sarah Kreps, Jérémy Sroussi, Virginie Barraud‐Lange, Jérôme Alexandre, François Goldwasser, Camille Tlemsani, Catherine Poirot   +11 more
wiley   +1 more source

When is a GIST not a GIST? A case report of synchronous metastatic gastrointestinal stromal tumor and fibromatosis [PDF]

, 2009
Background A number of non-malignant diseases that share similar morphological features as gastrointestinal stromal tumor (GIST) have been reported. Co-existence of GIST with these other diseases is rarely recognized or reported.
Chee Khoon Lee, Alison Hadley, Keshani Desilva, Gareth Smith, David Goldstein, G Demetri, R Yantiss, H Ehrlich, A Al-Attar, J Desai, S Cheon, M Li, M Heinrich, J Mace, R Chugh, M Penel, J Jagadeesan, K Hobson, J Monihan, J Lee   +19 more
core   +4 more sources

Multiple rapidly growing desmoid tumors that were difficult to distinguish from recurrence of rectal cancer

World Journal of Surgical Oncology, 2017
Background Intra-abdominal desmoid tumors are usually slow growing and solitary, but multifocal desmoid tumors develop on rare occasions. Diagnosing desmoid tumors before histological examination of a surgical biopsy is often difficult. In particular, if
Koki Nakanishi, Dai Shida, Shunsuke Tsukamoto, Hiroki Ochiai, Junichi Mazaki, Hirokazu Taniguchi, Yukihide Kanemitsu   +6 more
doaj   +1 more source

Bias and Fairness in Radiomics: A Comparative Analysis of Machine Learning Models on Four Oncology Datasets

International Journal of Imaging Systems and Technology, Volume 36, Issue 2, March 2026.
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, Jerónimo Hernández‐González, Vien Ngoc Dang, Marina Camacho, Karim Lekadir, Martijn P. A. Starmans   +5 more
wiley   +1 more source

Huge intrathoracic desmoid tumor

Annals of Thoracic Medicine, 2009
Desmoid tumors are soft-tissue neoplasms arising from fascial or musculo-aponeurotic structures. Most reported thoracic desmoid tumors originate from the chest wall. However, intrathoracic desmoid tumors are rare.
Ibrahim Majdi, Sandogji Hasan, Allam Abdullah   +2 more
doaj  

Vascular Reconstruction in Extremity Soft Tissue Sarcomas: A Systematic Review and Single‐Arm Meta‐Analysis

Journal of Surgical Oncology, Volume 133, Issue 4, Page 486-510, March 15, 2026.
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, Bernardo Fontel Pompeu, Vinícius dos Santos Macedo, Gabriel Henrique Acedo Martins, Eric Pasqualotto, Matheus Reginato Araujo, Julia Hoici Brunini, Victor Andrade Nunes, Cláudia Theis, Samuel Aguiar Junior   +9 more
wiley   +1 more source

Desmoid-type fibromatosis tumor in children: A narrative review of the literature

Saudi Journal of Oral Sciences
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, Abdulrahman Ibrahim Alhilal, Faris Abdullah Alghamdi, Yazeed Musaid Aldeghaither, Bader Fatani   +4 more
doaj   +1 more source