Zobrazeno 1 - 10
of 9 165
pro vyhledávání: '"synovial sarcoma"'
Autor:
Prerna Chadha, Meenakshi Kamboj, Sunil Pasricha, Vikas Arora, Vishal Yadav, Manoj Gupta, Anurag Mehta
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Spindle epithelial tumor with thymus-like elements (SETTLE) is a rare malignant neoplasm of the thyroid gland which is believed to arise from intrathyroidal thymic tissue. It predominantly affects young adults and children presenting with a
Externí odkaz:
https://doaj.org/article/1c37762a8e1b43f49f80d6b04ec8317c
Autor:
Ho Xuan Tuan, MD, PhD, Trinh Anh Tuan, MD, Nguyen-Thi Tam, MD, Ho Duc Cong, MD, Ngo Quang Duy, MD, Nguyen Duy Hung, MD, PhD, Luc Ceugnart, MD, Nguyen Minh Duc, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3456-3460 (2024)
Synovial sarcoma (SS) is an uncommon malignant tumor, ranking third in prevalence within the soft tissue sarcomas group. The vast majority of synovial sarcomas are present in the extremities, with only 15% developing in the retroperitoneal space. Ret
Externí odkaz:
https://doaj.org/article/189fd97b156747909a449bd620a8d715
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Background Synovial sarcoma is a rare soft tissue malignancy, occasionally found in the head and neck region. The diagnosis necessitates a multidisciplinary approach involving the clinical presentation, proper imaging studies and histologica
Externí odkaz:
https://doaj.org/article/2d955d541d5648969daeaa5a689e9c14
Autor:
Supraja Laguduva Mohan, Ekta Dhamija, Sameer Bakhshi, Prabhat Singh Malik, Sameer Rastogi, Chandrashekhara Sheragaru Hanumanthappa, Deepali Jain, Rambha Pandey
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 34, Iss 03, Pp 390-404 (2024)
Background Primary lung sarcoma (PLS) differs in management protocols and prognosis from the more common primary lung carcinoma (PLC). It becomes imperative to raise a high index of suspicion on radiological and pathological features.
Externí odkaz:
https://doaj.org/article/cc980dd7693d4bb5b6d51ce336de2627
Autor:
Saeed Montazeri, Mohsen Ayati, Mohammad Reza Nowroozi, Erfan Amini, Seyed Ali Momeni, Tahereh Yousefi, Maryam Azizi, Laleh Sharifi
Publikováno v:
Urology Case Reports, Vol 55, Iss , Pp 102766- (2024)
Synovial sarcoma, a rare soft tissue malignancy typically arising from synovial tissue, primarily manifests in the extremities but it may uncommonly present in other locations such as kidneys. Primary renal synovial sarcoma is an uncommon sarcoma wit
Externí odkaz:
https://doaj.org/article/d98fd4e014bb413c9baefb9b1f513c17
Autor:
Elnaz Khosh, MD, Arya Kazemi, MD, Elahe Abbaspour, MD, Sanaz Vahdati, MD, Maryam Sadat Mirenayat, MD, Siavash Ghaderi-Sohi, MD, Sara Haseli, MD, Elham Askari, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5262-5267 (2024)
Synovial sarcoma is a rare type of soft tissue sarcoma that typically arises in the lower extremities and rarely in the upper extremities. Here, we present an unusual case of a middle-aged man who complained of dyspnea, dry cough, and chest pain and
Externí odkaz:
https://doaj.org/article/d66d355dcd32496196e01d7d05375cc9
Autor:
Tom Vandaele, Jan Van Slambrouck, Patrick Schöffski, Herlinde Dumez, Birgit Weynand, Raf Sciot, Annalisa Barbarossa, An-Lies Provoost, Kristof Van de Voorde, Yves Debaveye, Sofian Bouneb, Philippe Nafteux, Laurens J. Ceulemans
Publikováno v:
World Journal of Surgical Oncology, Vol 22, Iss 1, Pp 1-12 (2024)
Abstract Background Pleural neoplasms are rare and can be subdivided into pleural metastasis and primary pleural neoplasms. Non-mesothelioma primary pleural neoplasms are a diverse group of extremely rare pathologies. Case presentation In this case s
Externí odkaz:
https://doaj.org/article/3b9699ca8efa44beb4a7a5afbe584a46
Autor:
Binyue Wang, Ligang Liu
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-5 (2024)
Abstract Synovial sarcoma of the heart is a rare tumor. Herein we would like to report a case of giant intrapericardial cardiac synovial sarcoma that originated from the right ventricle and grew outward near the diaphragm. After making adequate preop
Externí odkaz:
https://doaj.org/article/b93b0ddf45dc480f86c4f0a9d2167abd
Publikováno v:
EFORT Open Reviews, Vol 9, Iss 3, Pp 190-201 (2024)
Synovial sarcoma is a rare and highly malignant soft tissue sarcoma. The inconspicuous and diversity of its early symptoms make it a highly misdiagnosed disease. The management of synovial sarcomas is challenging as they are rare and have a poor prog
Externí odkaz:
https://doaj.org/article/b7d666c6c6fb4ffb959c296fe0b9face
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 34, Iss 01, Pp 156-159 (2024)
Synovial sarcomas are rare malignant mesenchymal soft tissue tumors. We presented the case of a 53-year-old woman patient presenting with acute deep vein thrombosis, later diagnosed as a deep synovial sarcoma of the femoral vein wall. The tumor was i
Externí odkaz:
https://doaj.org/article/3c64cf5e756f4a05897ee4d4a3a70a8f