Results 61 to 70 of about 8,818 (223)
When is a GIST not a GIST? A case report of synchronous metastatic gastrointestinal stromal tumor and fibromatosis [PDF]
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 +19 more
core +3 more sources
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
Recalcitrant desmoid tumor of the abdominal wall: A reconstructive dilemma
Desmoid tumors are slow-growing benign tumors. These tumors infiltrate surrounding tissues but not malignant and associated with women of fertile age, especially during and after pregnancy. We report a young male patient with a recurrent desmoid tumor of
Prakash Chandra Kala +3 more
doaj +1 more source
Surgical management of recurrent desmoid tumor in a young male
Desmoid tumors are rare, aggressive fibroblastic soft tissue tumors. We report a case of a 20-year-old male with recurrence of desmoid tumor of the left shoulder after initial complete resection 3 years prior. Pathology revealed fibromatosis desmoid type.
Omar A. Santiago Báez +4 more
doaj +1 more source
Digital PCR analysis of circulating tumor DNA: a biomarker for chondrosarcoma diagnosis, prognostication, and residual disease detection [PDF]
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
Rib Ewing Sarcomas in Children and Young Adults: A Large National Retrospective Series
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
Huge intrathoracic desmoid tumor
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 +2 more
doaj
Sporadic Right Lumbar Intraabdominal Desmoid Tumor: A Case Report
Sporadic intraabdominal desmoid tumor is a rare occurrence, comprising 0.03% of all neoplasms. It has an estimated incidence of 2 to 4 per million in the general population. Only 15% of all desmoid tumors are intraabdominal.
Ong Xin Zen +4 more
doaj +1 more source
Thoracic Actinomycosis: A Rare Cause of Pleural Thickening
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
An Unusual Location of Intra-Abdominal Desmoid Tumor
Desmoid tumors are locally aggressive benign neoplasms which are predominantly found in young women. Here we present a 36-year-old woman with histopathologically proven renal desmoid tumor.
Ahmet Hakan Haliloğlu +4 more
doaj +1 more source

