Results 21 to 30 of about 16,784 (197)

Primary synovial sarcoma of the brain in a 35-year-old patient: A rare clinical experience

Journal of Clinical and Scientific Research, 2023
Synovial sarcoma is an aggressive soft-tissue sarcoma with a poor prognosis and has an origin of uncertain histology. It frequently presents as a localised disease, especially near large joints around the knee and thigh.
P Harika Bhavani, B V Subramanian, Pranabandhu Das, A Y Lakshmi, N Rukmangadha   +4 more
doaj   +1 more source

Synovial sarcoma in a neonate

Indian Pediatrics, 2016
Malignant tumors in neonates are rare.A tumor was detected in the left biceps of a 3-day old neonate. Tumor biopsy and molecular study confirmed the diagnosis of synovial sarcoma. The child received multi-modality treatment with surgery and chemotherapy.The child is disease-free on follow-up period of 12 months.Synovial sarcoma can rarely occur in a ...
Venkatraman, Radhakrishnan, Anjana, Joel, Shirley, Sundersingh, Anand, Raja   +3 more
openaire   +2 more sources

Pulmonary synovial sarcoma: A case series and review of literature

Asian Journal of Medical Sciences, 2022
Synovial sarcoma is a rare malignant mesenchymal tumor that can develop at any anatomic site. Pulmonary sarcomas constitute 0.1–0.5% of all primary lung malignancies. Primary pulmonary synovial sarcoma is highly uncommon.
Amrutha Peter , Amarendra Kumar Shukla , Manish Kumar Gupta , Vikas Patel , Vijaya Kumar , Veerendra Arya , Pawan Tiwari , Jitendra Kishore Bhargava   +7 more
doaj   +1 more source

Submandibular synovial sarcoma mimicking a vascular lesion: A rare case report

SRM Journal of Research in Dental Sciences, 2018
Synovial sarcoma is a soft-tissue sarcoma of periarticular surfaces in close association with tendon sheaths, bursae, and joint capsules. Synovial sarcoma represents 5.6%–10% of all soft-tissue sarcomas.
Naresh Kumar, Neeraj Kumar Dhiman, Shankar Singh, Ajit Kumar Vishwakarma   +3 more
doaj   +1 more source

Synovial sarcoma of submandibular gland with aberrant P63 expression a case report of rare event

Human Pathology: Case Reports, 2019
Synovial sarcoma is a tumor commonly involves extremities and periarticular soft tissue of young adults. Head and neck region is involved in 10% of cases, mostly biphasic in histology.
Afnan Elsayed, Haneen Al-Maghrabi, Hosam Alardati, Ameen Alherabi, Abdelrazak Meliti   +4 more
doaj   +1 more source

Synovial-cell sarcoma.

The Pan African medical journal, 2019
Thirty-nine years old patient presented to the emergency department with left-sided chest pain for four months and 4kg weight loss through the same period. Physical examination showed bulging of the left scapula which is tender to touch and decreased breath sounds on the left side.
Ahmed Nugud, Shomous Nugud
openaire   +4 more sources

NKp44-based chimeric antigen receptor effectively redirects primary T cells against synovial sarcoma

Translational Oncology, 2022
Background: T-cell receptor-engineered T-cell therapies have achieved promising response rates against synovial sarcoma in clinical trials, but their applicability is limited owing to the HLA matching requirement.
Yudai Murayama, Yasushi Kasahara, Nobuhiro Kubo, Chansu Shin, Masaru Imamura, Naoki Oike, Takashi Ariizumi, Akihiko Saitoh, Minori Baba, Tomohiro Miyazaki, Yuko Suzuki, Yiwei Ling, Shujiro Okuda, Keichiro Mihara, Akira Ogose, Hiroyuki Kawashima, Chihaya Imai   +16 more
doaj   +1 more source

Renal synovial sarcoma: Considerations for radical nephrectomy- a case report and literature review

Urology Case Reports
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.
Saeed Montazeri, Mohsen Ayati, Mohammad Reza Nowroozi, Erfan Amini, Seyed Ali Momeni, Tahereh Yousefi, Maryam Azizi, Laleh Sharifi   +7 more
doaj   +1 more source

Intraneural synovial sarcoma of the tibial nerve

Rare Tumors, 2018
Synovial sarcomas are malignant soft tissue tumors that carry a metastatic potential and portend poor prognoses. We report a very rare synovial sarcoma arising from the tibial nerve and describe its successful treatment including limb preservation.
Kazuhiko Hashimoto, Shunji Nishimura, Kousuke Fujii, Ryosuke Kakinoki, Masao Akagi   +4 more
doaj   +1 more source

Organoids in pediatric cancer research

FEBS Letters, EarlyView.
Organoid technology has revolutionized cancer research, yet its application in pediatric oncology remains limited. Recent advances have enabled the development of pediatric tumor organoids, offering new insights into disease biology, treatment response, and interactions with the tumor microenvironment.
Carla Ríos Arceo, Jarno Drost
wiley   +1 more source