Results 51 to 60 of about 10,048 (219)

Next-generation sequencing is highly sensitive for the detection of beta-catenin mutations in desmoid-type fibromatoses

, 2015
Desmoid-type fibromatoses are locally aggressive and frequently recurrent tumours, and an accurate diagnosis is essential for patient management. The majority of sporadic lesions harbour beta-catenin (CTNNB1) mutations. We used next-generation sequencing
Amary, M.F., Tirabosco, R., Aitken, S.J., Dileo, P., Presneau, Nadège, Berisha, F., Flanagan, A.M., Kalimuthu Sangeetha   +7 more
core   +1 more source

Hereditary desmoid disease [PDF]

, 2007
Review on Hereditary desmoid disease, with data on clinics, and the genes ...
Scott, JR
core   +1 more source

Desmoid tumor of the abdominal wall: case report

PAMJ Clinical Medicine, 2020
Desmoid tumors are rare fibrous tumors of the soft tissues. Develops on the abdominal wall, in the abdomen, or extra-abdominal. Parietal location is very common among women. Hormonal factors are incriminated.
Kaoutar Achehboune, Hanane Baybay, Khadija Issoual, Sara Elloudi, Fatima Zahra Mernissi   +3 more
doaj   +1 more source

Desmoid Tumor and Implant-Based Breast Reconstruction

Case Reports in Oncology, 2023
Desmoid tumors are rare locally aggressive myelodysplastic tumors that are usually abdominally based. They account for 0.2% of breast tumors. Certain factors like prior surgery, familial adenomatous polyposis, pregnancy, and high estrogen states are ...
Catherine Kilmartin, Clinton Westover, Shyam Raghavan, Patrick M. Dillon, Chris A. Campbell   +4 more
doaj   +1 more source

Prevalence and Risk Factors for Financial Toxicity Among Sarcoma Patients During and Following Treatment Across the Lifespan

Cancer Reports, Volume 9, Issue 10, October 2026.
ABSTRACT Background Financial toxicity (FT) describes the impact of cancer and treatment‐related financial burden. We evaluated the prevalence and risk factors for FT among sarcoma patients. Methods A sarcoma cohort was constructed to assess health outcomes.
Michael J. Robinson, Lili Sun, Tatsuki Koyama, Emma A. Schremp, Grace Aronoff, Tulio Guimaraes, Taylor A. Stokes, Elizabeth J. Davis, Vicki Keedy, Scott C. Borinstein, Herbert S. Schwartz, Jennifer L. Halpern, Joshua M. Lawrenz, Daniel Johnson, Timothy Su, Leo Luo, Travis Osterman, Tuya Pal, Ben H. Park, Xiao‐Ou Shu, Debra L. Friedman, Eric T. Shinohara   +21 more
wiley   +1 more source

Combination of Anlotinib and Celecoxib for the Treatment of Abdominal Desmoid Tumor: A Case Report and Literature Review

Frontiers in Oncology, 2022
Desmoid tumor is a rare disease, which is histologically characterized by local invasion, monoclonality, and fibroblast proliferation; and clinically characterized by a variable and often unpredictable course.
Jianzheng Wang, Hongle Li, Hui Wang, Qingli Li, Xuanye Bai, Huifang Lv, Caiyun Nie, Beibei Chen, Weifeng Xu, Shuiping Tu, Xiaobing Chen   +10 more
doaj   +1 more source

A Case of Primary Intramedullary Infantile Fibrosarcoma With an RBPMS::NTRK3 Fusion and Response to Larotrectinib

Neuropathology and Applied Neurobiology, Volume 52, Issue 5, October 2026.
We report a case of primary intramedullary infantile fibrosarcoma (IFS) in a 4‐week‐old infant with rapidly progressive cervical myelopathy. Histology showed a spindle cell tumour with diffuse S100 and pan‐TRK expression. RNA sequencing identified an RBPMS::NTRK3 fusion.
Mégane Le Quang, Julie Tandonnet, Nathalène Truffaux, Lucile Vanhersecke, Jean Delmas, Arthur Durouchoux, Dorian Bochaton, Arnault Tauziède‐Espariat, Guillaume Chotard   +8 more
wiley   +1 more source

Perineurioma‐like EMA‐positive calvarial neoplasms: clinicopathological study of eight cases

Histopathology, Volume 89, Issue 3, Page 544-553, September 2026.
Perineurioma‐like, EMA‐positive calvarial neoplasms (PLECN) are a rare group of intraosseous spindle cell tumours that demonstrate overlapping morphologic features of perineurioma and fibroblastic meningioma. These lesions tend to behave indolently but show a propensity for progressive growth.
Raheel Rizwan, Yingting Mok, Josephine K Dermawan, Alexandra Isaacson, Veronica Ulici, Scott E Kilpatrick, John D Reith, Gabrielle Yeaney, Hakan Ilaslan, Karen J Fritchie   +9 more
wiley   +1 more source

Laparoscopic-Assisted Percutaneous Cryoablation of Abdominal Wall Desmoid Fibromatosis: Case Series and Local Experience

Surgical Techniques Development
Background: Desmoid tumors (DTs) are rare, non-metastatic but locally aggressive connective tissue neoplasms. While standard treatments include surgery, radiation, and ablation, current guidelines advocate active surveillance unless tumors progress or ...
Kadhim Taqi, Jaymie Walker, Cecily Stockley, Antoine Bouchard-Fortier, Stefan Przybojewski, Lloyd Mack   +5 more
doaj   +1 more source

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