Results 51 to 60 of about 4,737 (170)

Comparative Analysis of a Dual DNA–RNA Panel and a DNA‐Only Panel for Sarcoma: Real‐World Data From a Nationwide Genomic Database

Cancer Science, Volume 117, Issue 1, Page 156-168, January 2026.
Dual DNA–RNA panel with matched tumor–normal testing may improve diagnostic accuracy and inform treatment decisions in the routine clinical management of sarcoma. ABSTRACT Next‐generation sequencing‐based comprehensive cancer genomic profiling is promising in cancer management; however, most studies rely on tumor‐only DNA panels from single ...
Eiji Nakata, Kiichiro Ninomiya, Tatsunori Osone, Daisuke Ennishi, Shuta Tomida, Tomohiro Fujiwara, Toshiyuki Kunisada, Mashu Futagawa, Akira Hirasawa, Shinichi Toyooka, Toshifumi Ozaki   +10 more
wiley   +1 more source

Open surgical treatment for rare epithelioid hemangioendothelioma of the common femoral vein

Journal of Interventional Medicine, 2019
Epithelioid hemangioendothelioma is a very rare disease affecting big blood vessels, especially veins. There have been very few articles describing the disease.
Xiangjiang Guo, Shuo fei Yang, Guan hua Xue, Jia quan Chen, Hao Zhang, Lan Zhang   +5 more
doaj   +1 more source

Dual immunotherapy alternating with anti-PD-1 antibody plus liposomal doxorubicin show good efficacy in prostate epithelioid hemangioendothelioma: a case report

Frontiers in Immunology
Epithelioid hemangioendothelioma is a rare vascular malignancy, and currently, there is no standard treatment regimen for this disease and existing treatment options have limited efficacy.
Jie Zhang, Jie Zhang, Qin Ye, Xudan Yang, Tenglong Li, Shan Huang, Ping Zhou, Yumei Feng, Hao Liu, Ke Xie   +9 more
doaj   +1 more source

A Tragical Paediatric Case History of Intraorbital and Intracranial Epithelioid Hemangioendothelioma

Case Reports in Neurological Medicine, 2012
Epithelioid hemangioendothelioma (EHE) is a rare tumor of intermediate malignancy. We report a case of intracranial and intraorbitar EHE. A 3-year-old girl presented with a 3-month history of progressive left exophthalmia.
K. Aniba, M. Laghmari, M. Lmejjati, H. Ghannane, S. Ait Benali   +4 more
doaj   +1 more source

Mediastinal epithelioid hemangioendothelioma—Mimicker of mature teratoma

Radiology Case Reports, 2019
We report a case of an adult man who underwent surgical resection of a presumed anterior mediastinal teratoma, which upon histopathologic assessment was diagnosed as an epithelioid hemangioendothelioma (EHE). EHE is a rare vascular tumor of variable, but
Alexandre Semionov, Mutaz Khairo
doaj   +1 more source

Advances in the Diagnosis, Treatment, and Management of Liver Nodules: A Comprehensive Review

Portal Hypertension &Cirrhosis, Volume 4, Issue 4, Page 232-251, December 2025.
Liver nodules commonly occur due to various causes, some of which are malignant or may undergo malignant transformation, leading to disease progression or delayed detection in clinical practice. The widespread use of imaging methods has increased the detection rate of liver nodules. Furthermore, precision medicine techniques and artificial intelligence
Chang Gao, Dongyang Chen, Youpeng Chen
wiley   +1 more source

Clinical and biological factors associated with response to immune checkpoint inhibitors in advanced sarcomas: IMPRESARC, a French retrospective multicenter cohort study

Cancer, Volume 131, Issue 18, 15 September 2025.
Abstract Background Immune checkpoint inhibitors (ICIs) in unselected sarcomas yield limited response rates and tumor control. Long‐term responders have however been reported, suggesting a critical challenge in refining patient selection, by identifying reliable predictive factors for response. Methods The authors conducted a multicenter, retrospective
Mina Fazel, Romain Varnier, Hélène Vanacker, Nicolas Penel, Sarah Watson, Benjamin Verret, Thibaud Valentin, Emmanuelle Bompas, Waisse Waissi, Alexandra Meurgey, Françoise Ducimetière, Jean‐Yves Blay, Armelle Dufresne, Mehdi Brahmi   +13 more
wiley   +1 more source

Hemangioendotelioma epitelial: um tumor raro com apresentação atípica

Galicia Clínica, 2016
Epithelioid Hemangioendothelioma is a rare neoplasia, and has its origin in the vascular endothelium. It may grow in several organs and tissues. There is not any approved therapeutic scheme and the prognosis is unpredictable.
Madalena Reis, Alcina Tavares, Luís Ferreira, Lina De Carvalho   +3 more
doaj   +1 more source

YAP1::KMT2A‐Rearranged Sarcoma: Report of a New Case With Unusual Morphology and Immunohistochemical Features

Genes, Chromosomes and Cancer, Volume 64, Issue 7, July 2025.
ABSTRACT Recurrent KMT2A and YAP1 related fusions have recently been reported in various mesenchymal neoplasms of different histogenesis. First, YAP1::KMT2A fusions have been described in a subset of MUC4‐negative sclerosing epithelioid fibrosarcomas (SEF), while VIM::KMT2A fusions in a handful of cases associated with an undifferentiated spindle cell ...
Caterina Fumagalli, Ruth Orellana, Sílvia Bagué, Malena Ferré, Allan Gonzalez, Lluis Catasús, Jaume Llauger, Ana Peiró, Paul Zamora Alarcón, Katarina Majercakova, Raúl Terés, Marie Karanian‐Philippe, Franck Tirode, Cristina R. Antonescu   +13 more
wiley   +1 more source

Low-Grade Uterine Epithelioid Hemangioendothelioma Presented as a Submucosal Leiomyoma during Labor

Case Reports in Pathology, 2013
With the exception of leiomyomas, soft tissue tumors of the uterine corpus are not common. This is particularly true for vascular neoplasms, with the epithelioid hemangioendothelioma being a curiosity; not more than twenty-two cases of malignant ...
Anastasios V. Koutsopoulos, Efthimios Sivridis, Panagiotis Tsikouras, Vasileios Liberis, Georgia Karpathiou, Alexandra Giatromanolaki   +5 more
doaj   +1 more source