Results 71 to 80 of about 8,831 (160)

Impact of tissue staining and scanner variation on the performance of pathology foundation models: a study of sarcomas and their mimics

The Journal of Pathology: Clinical Research, Volume 12, Issue 2, March 2026.
Abstract Histopathological analysis is considered the gold standard for the diagnosis and prognostication of cancer. Recent advances in AI, driven by large‐scale digitisation and pan‐cancer foundation models, are opening new opportunities for clinical integration.
Binghao Chai, Jianan Chen, Paul Cool, Fatine Oumlil, Anna Tollitt, David F Steiner, Tapabrata Chakraborti, Adrienne M Flanagan, Adrienne M Flanagan, Anna Tollit, Fatine Oumlil, Fernanda Amary, Roberto Tirabosco, Nischalan Pillay, Paul Cool, Adam Levine, Sebastian Brandner, Angela Richard‐Londt, Petra Balogh, Phillipe Taniere, Preethi Gopinath, Neil Sebire, Luis Campos, Thomas Jacques, Sarah Coupland, Katalin Boros, Edmund Cheesman, Elizabeth Halloran, Caroline Glennie, Leona Doyle, Adrian Marino‐Enriquez, Jonathan Davey, Hannah Monaghan, Michael Toss, David Hughes, Malee Fernando, David Leff, Patrick Shenjere, Oisin Houghton, Tom McCulloch, Filomena Medeiros, Ann Sandison, Kalnisha Naidoo, Getnet Demissie, Heena Patel, Uchechi Igbokwe, Graham Thwaites, Keeley Thwaites, Ann Fleming, Mercy Berin, Shyamala Fernandez, Rajesh Nalluri, Zahra Atiyyah, Konrad Wolfe, Victoria Hills, Tomos Saunders, Matilda Ralph, Nicholas Southgate, Francesca Maggiani, Zsolt Orosz, Jennifer Brown, Nick Athanasou, Ian Cook, Sarah Oliver, Peter Davis, Shelley Brown, Jasenka Mazibrada, Nathan Asher, Efren Quilala, Dalian Beaver, Izhar Bagwan, Dawn Whyndham, Khin Thway, Michael Hubank, Janet Shipley   +74 more
wiley   +1 more source

An update on the management of sporadic desmoid-type fibromatosis: a European Consensus Initiative between Sarcoma PAtients EuroNet (SPAEN) and European Organization for Research and Treatment of Cancer (EORTC)/Soft Tissue and Bone Sarcoma Group (STBSG) [PDF]

, 2017
Desmoid-type fibromatosis is a rare and locally aggressive monoclonal, fibroblastic proliferation characterized by a variable and often unpredictable clinical course.
Verhoef, K., Gronchi, Alessandro, Garcia, J, van der Graaf, W T, Baumgarten, C., Haller, F., Graaf, W.T.A. van der, van Der Graaf, W. T., Haller, F, Penel, Nicolas, Lindner, L. H., Desmoid Working Group, Messiou, C, Gronchi, A, Penel, N, Bonvalot, S., Gronchi, A., Haas, R., Haas, R, Kasper, B, Bonvalot, S, Kasper, Bernd, Baumgarten, C, Kasper, B., Garcia, J., Bonvalot, Sylvie, Hohenberger, P., van der Graaf, W. T.; id_orcid, van der Graaf, WT, Penel, N., Messiou, C., Desmoid Working Group,, Bauer, S., Hohenberger, P, Desmoid Working Grp   +34 more
core   +2 more sources

Breast Fibromatosis in a Patient With a History of Treated Breast Cancer: A Case Report

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Desmoid tumors are benign mesenchymal neoplasms that originate from muscular fasciae and aponeuroses. Breast involvement is exceptionally rare, accounting for less than 0.2% of all breast tumors. A 41‐year‐old woman with a history of right‐sided invasive ductal carcinoma (IDC) diagnosed in 2022 underwent breast‐conserving surgery (BCS) and ...
Saba Ebrahimian, Sakineh Soleimani Varaki, Faezeh Zabihi   +2 more
wiley   +1 more source

Chest wall fibromatosis with congenital muscular torticollis: Two forms of deep fibromatosis in a child

Journal of Indian Association of Pediatric Surgeons, 2018
Desmoid tumors (fibromatosis) are intermediate grade, locally aggressive soft-tissue tumors. A rare case of chest wall fibromatosis in a girl with congenital muscular torticollis is being reported.
Sachit Anand, Anjan K Dhua, Veereshwar Bhatnagar, Devasenathipathy Kandasamy, Sudheer Arava   +4 more
doaj   +1 more source

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

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

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 Fibromatosis of Breast Resembling Carcinoma: A Diagnostic Conundrum

Medical Journal of Dr. D.Y. Patil Vidyapeeth
Desmoid fibromatosis of the breast is an uncommon, benign, and locally invasive fibroblastic tumor that may show signs of malignancy but cannot spread.
Yaminy Pradeep Ingale, Tejasweeni Shrirao, Arpana Dharwadkar, Vidya Viswanathan   +3 more
doaj   +1 more source

Complete resection of a rectus abdominis muscle invaded by desmoid tumors and subsequent management with an abdominal binder: a case report

Journal of Medical Case Reports, 2018
Background Desmoid-type fibromatosis is characterized by desmoid tumors, which are benign soft tissue tumors that can be locally aggressive but typically do not metastasize.
Tatsuhiko Ogawa
doaj   +1 more source

Aggressive Fibromatosis (Desmoid Tumor) Is Derived from Mesenchymal Progenitor Cells

, 2010
The cellular origins from which most tumors arise are poorly defined, especially in mesenchymal neoplasms. Aggressive fibromatosis, also known as desmoid tumor, is a locally invasive soft tissue tumor that has mesenchymal characteristics.
Saied Nik-Amini, Colleen Wu, Puviindran Nadesan, Benjamin A. Alman, William L. Stanford   +4 more
core   +1 more source