Results 71 to 80 of about 16,784 (197)

Increased Risk of Sarcomas in Children With Congenital Anomalies: Findings From the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Registry Linkage Study

Pediatric Blood &Cancer, Volume 73, Issue 8, August 2026.
ABSTRACT Background Pediatric sarcomas are a heterogeneous group of tumors that contribute disproportionately to cancer mortality in children. Although congenital anomalies are among the strongest known risk factors for childhood cancer, the risk of specific sarcoma subtypes among affected individuals has not yet been thoroughly evaluated. Procedure We
Russ Wolters, Ji Yun Tark, Tiffany M. Chambers, Tania A. Desrosiers, Michael E. Scheurer, Charles Shumate, Wendy N. Nembhard, Mahsa M. Yazdy, Eirini Nestoridi, Amanda E. Janitz, Jean Paul Tanner, Russell S. Kirby, Jason L. Salemi, Yao Yu, Chad D. Huff, Sharon E. Plon, Philip J. Lupo, Jeremy M. Schraw   +17 more
wiley   +1 more source

What's Your Diagnosis? Large Mediastinal Mass in a Dog

Veterinary Clinical Pathology, EarlyView.
Rosane O. Cruz, Talles M. Almeida, Iris D. S. Menezes, Ludmila R. Moroz, Suane N. Boaventura, Tiago Peixoto, Stella F. Valle, Nicole Hlavac   +7 more
wiley   +1 more source

MEIS1::NCOA2 Rearranged Spindle Cell Neoplasm of Vulva With Unusual Low‐Grade Morphology

Genes, Chromosomes and Cancer, Volume 65, Issue 8, August 2026.
ABSTRACT MEIS1::NCOA2 is a recurrent gene fusion that has been predominantly identified in primitive sarcomas arising within the genitourinary and gynecological tracts. Since its initial description in 2018, an increasing number of cases have been reported, further defining the clinicopathological spectrum of this entity.
Pinki Soni, Liyan Song, Jason Phung, Andrew Colebatch, John M. Gross, Pedram Argani, Pranav Dorwal   +6 more
wiley   +1 more source

Primary pleural synovial sarcoma with repeated resection leading to long‐term survival

Respirology Case Reports, 2019
Primary pleural synovial sarcoma is a malignant tumour and thought to be more aggressive than synovial sarcoma which occurs in extremities. Its treatment strategy has not been fully established because of its rarity.
Naoko Katsurada, Hisashi Ohnishi, Miho Ikeda, Naoe Jimbo, Yukihisa Hatakeyama, Kayoko Okamura   +5 more
doaj   +1 more source

Primary pleuropulmonary synovial sarcoma mimicking a carcinoid tumor: Case report and literature review

Radiology Case Reports, 2016
Primary pleuropulmonary synovial sarcoma is a rare malignancy. Commonly described radiologic features in the literature include pleural disease and/or effusion, lack of calcification and high uptake on positron emission tomography computerised tomography.
Zeid Al-Ani, MBChB, MRCP, FRCR, Jawad Naqvi, MBChB, Teik Chooi Oh, FRCR   +2 more
doaj   +1 more source

Synovial Sarcoma [PDF]

Ear, Nose & Throat Journal, 2006
Gretchen S, Folk, Lester D R, Thompson
openaire   +2 more sources

Urokinase Plasminogen Activator Receptor‐Associated Protein (uPARAP) as a Potential Next Generation Molecular Target for Treatment of Gastrointestinal Stromal Tumors (GIST)

International Journal of Cancer, Volume 159, Issue 3, Page 797-808, 1 August 2026.
A key component of the collagen internalization and lysosomal degradation cellular machinery, uPARAP may contribute to cancer progression. Here, the authors explored the expression of uPARAP in gastrointestinal stromal tumors using well‐annotated clinical patient samples and specimens from cell line‐ and patient‐derived xenografts.
Chao‐Chi Wang, Flavia Paternostro, Agnieszka Wozniak, Lore De Cock, Luna De Sutter, Kimberly Verbeeck, Ulla Vanleeuw, Daniël Gorgels, Che‐Jui Lee, Raf Sciot, Patrick Schöffski   +10 more
wiley   +1 more source

Rare presentation of primary intra-articular synovial sarcoma of knee joint with insights from literature review

Indian Journal of Pathology and Microbiology
Synovial sarcoma is a rare and malignant soft tissue tumor, comprising 5%–10% of such cases. This tumor primarily afflicts adolescents and young adults, with slight male bias, often near large joints like the knee and hip.
Guralarasan Gurubalan, Surabhi, Madhu Kumari, Ritesh Pandey, Punam P. Bhadani, Abinaya Marikannu   +5 more
doaj   +1 more source

Monophasic epithelial synovial sarcoma initially diagnosed as metastatic adenocarcinoma of unknown primary

Human Pathology: Case Reports, 2019
Monophasic epithelial synovial sarcoma is extremely rare, and its existence has been debated. We report a case of monophasic epithelial synovial sarcoma, which was initially diagnosed as metastatic adenocarcinoma.
Donghwa Baek, Andreia Barbieri, Alberto G. Ayala, Kwang M. Lee, Myoung J. Ju, Jae Y. Ro   +5 more
doaj   +1 more source

GI Synovial Sarcomas

Clinical and Translational Gastroenterology, 2012
Synovial sarcoma accounts for about 10% of adult soft tissue sarcomas, with 80–90% located in the limbs. Gastrointestinal tract involvement is rare. Synovial sarcoma has a propensity for local recurrence and lung metastases, which can be delayed beyond 5 years.
Sinniah, Rajeev Palar, Roche, Enrico, Cameron, Donald   +2 more
openaire   +2 more sources