Fibromatosis extraabdominal agresiva: descripción de un caso y revisión de la literatura [PDF]
, 2009 El tumor desmoide es un raro tumor benigno de partes blandas, con gran capacidad invasiva local y sin potencial metastático. Se han descrito diversas variedades según su localización; siendo la variedad extraabdominal ó fibromatosis extraabdominal ...
Fernández Gabarda, Rafael +2 more
core
iMeta, Volume 5, Issue 2, April 2026.Spatial multi‐omics defines a DLL4–NOTCH3–driven capillary–mCAF axis orchestrating fibrotic remodeling and immune exclusion in hepatocellular carcinoma tumor cores, conferring immune checkpoint blockade resistance. Targeting stromal NOTCH3 disrupts this pro‐fibrotic niche, enhances T cell infiltration, and synergizes with anti‐PD‐1 therapy ...
Fansen Ji +18 more
wiley +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 +5 more
doaj +1 more source
Extra-Abdominal Desmoid-Type Fibromatosis Mimicking Myxofibrosarcoma
Journal of the Belgian Society of Radiology, 2022 A 27-year-old woman was confirmed to have extraabdominal desmoid-type fibromatosis. Desmoid-type fibromatosis is a very rare connective tissue neoplasm with the extraabdominal type even more rare.
Ye Rin Kim, Yu Sung Yoon, Hyerim Park
doaj +1 more source
Desmoid tumor of the abdominal wall preoperatively suspected as urachal tumor: a case report [PDF]
, 1992 A case of desmoid tumor of the abdominal wall which was preoperatively suspected as urachal tumor is presented. The patient was a 56-year-old man, who was referred to our clinic for further examination of the mass detected incidentally in the ventral ...
安永, 豊 +4 more
core
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 +7 more
core +1 more source
Rib Ewing Sarcomas in Children and Young Adults: A Large National Retrospective Series
Pediatric Blood &Cancer, Volume 73, Issue 4, April 2026.ABSTRACT Background and Purpose Ewing sarcoma (ES) is the most prevalent malignant thoracic tumor in childhood and young adults. This study reports the outcome of a national cohort treated in an international prospective trial for a localized rib ES, with a long follow‐up.
Audrey Claren +14 more
wiley +1 more source
Delayed phlegmon with gallstone fragments masquerading as soft tissue sarcoma. [PDF]
, 2016 Complications from lost gallstones after cholecystectomy are rare but varied from simple perihepatic abscess to empyema and expectoration of gallstones.
Bateni, Cyrus P +3 more
core +1 more source
Thoracic Actinomycosis: A Rare Cause of Pleural Thickening
Respirology Case Reports, Volume 14, Issue 4, April 2026.We report a case of a man who presented with a chest wall mass and was found to have pleural thickening on PET, with features concerning for mesothelioma. Further investigation revealed a diagnosis of actinomyces, a rare infectious cause of pleural thickening.
Evonne Shum +5 more
wiley +1 more source
Digital PCR analysis of circulating tumor DNA: a biomarker for chondrosarcoma diagnosis, prognostication, and residual disease detection [PDF]
, 2017 Conventional chondrosarcoma is the most common primary bone tumor in adults. Prognosis corresponds with tumor grade but remains variable, especially for individuals with grade (G) II disease.
Amary, F +14 more
core +1 more source