Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1055/a-1517-6975 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Correction to: Sclerosing epithelioid fibrosarcoma: a new mesenchymal non-meningothelial tumor involving the central nervous system?
Virchows Arch
December 2024
Department of Pathology, Strasbourg University Hospital, 67098, Strasbourg Cedex, France.
YAP1::KMT2A-rearranged sarcomas harbor a unique methylation profile and are distinct from sclerosing epithelioid fibrosarcoma and low-grade fibromyxoid sarcoma.
Virchows Arch
December 2024
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, 350 W. 11thStreet, Room 4086, Indianapolis, IN, 46202, USA.
Sclerosing epithelioid fibrosarcoma (SEF) was originally described as a peculiar variant of fibrosarcoma in 1995. Subsequent studies showed that conventional SEF was associated with both immunohistochemical expression of MUC4 and EWSR1/FUS gene rearrangements with CREB3L1 as the predominant fusion partner. Since then, a distinct group of fibrous tumors characterized by YAP1::KMT2A and KMT2A::YAP1 gene rearrangements and SEF-like morphology has been described.
View Article and Find Full Text PDFNon-metastatic causes of multiple pulmonary nodules.
Insights Imaging
November 2024
Department of Radiology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Article Synopsis
- Multiple pulmonary nodules can arise from either benign or malignant processes, with metastasis being a primary concern in patients with a known primary cancer.
- Differentiating between the causes of these nodules is complicated, as metastatic nodules can resemble those from infections, inflammation, and rare benign diseases.
- Radiological features, along with clinical and laboratory findings, play a crucial role in distinguishing between metastatic and non-metastatic causes of multiple pulmonary nodules, which is essential for accurate diagnosis and treatment.
Malignant Bone-Forming Neoplasm With NIPBL::BEND2 Fusion.
Genes Chromosomes Cancer
November 2024
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Conventional high-grade osteosarcomas are characterized by aggressive radiologic features, cytologic pleomorphism, and complex genomics. However, rare examples of osteosarcomas remain challenging due to unusual histology, such as sclerosing or osteoblastoma-like features, which may require molecular confirmation of their complex genetic alterations. We have encountered such a case in a 17-year-old man, who presented with a third metatarsal sclerotic bone lesion, found incidentally in the work-up of a foot trauma.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!