Results 91 to 100 of about 8,818 (223)

Undifferentiated Embryonal Sarcoma of the Liver in a 6 Years Old Male Patient: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Undifferentiated Embryonal Sarcoma of the Liver (UESL) is a rare, aggressive mesenchymal tumor predominantly affecting children. Its non‐specific clinical presentation and variable imaging characteristics often lead to diagnostic delays and complex management.
Rajab Msemo, Michael Machage, Novath Ngowi, Alex Mashaka, Elizabeth Sawaki, Ally Mwanga   +5 more
wiley   +1 more source

Fibromatosis of the neck causing airway obstruction managed effectively with weekly low-dose methotrexate and vinblastine [PDF]

, 2009
Fibromatosis is a rare disease with benign histology. Its infiltrative growth pattern may prevent complete resection. We report a case of a 40-year-old woman with fibromatosis of the neck requiring an emergency operation for acute upper airway ...
Sze, H, Yeung, MW
core  

Ovarian steroid cell tumor with biallelic adenomatous polyposis coli inactivation in a patient with familial adenomatous polyposis [PDF]

, 2012
Familial adenomatous polyposis (FAP) is an autosomal dominant cancer predisposition syndrome that accounts for approximately 0.5–1% of all colorectal cancer cases.
Abraham, Abraham, Aoki, Belchetz, Bertario, Blaker, Boerboom, Bonnet, Curia, Ellison, Fearon, Galle, Garcia-Rostan, Gaujoux, Groden, Groves, Half, Hamilton, Hayes, Hosogi, Ilyas, Korinek, Kurahashi, Lazar, Marchesa, Miyaki, Miyaki, Miyaki, Miyoshi, Morin, Nishisho, Scully, Segditsas, Shah, Smith, Stratakis, Wakatsuki   +36 more
core   +1 more source

Cytologic and Histologic Findings of Extrapleural Solitary Fibrous Tumor: Report of Two Cases

Diagnostic Cytopathology, Volume 54, Issue 2, Page E46-E53, February 2026.
ABSTRACT Solitary fibrous tumors (SFT) are a rare neoplasm of mesenchymal origin. SFT was previously described primarily in the pleura and meninges; however, extrapleural and extra‐meningeal SFT have been reported in almost every anatomic site and account for up to 40% of cases.
Michael Tyler, Katsiaryna Khatskevich, Chadi Hajar, Jack Yang, Hao Liu   +4 more
wiley   +1 more source

A case report of extra‐abdominal desmoid tumor after kidney transplantation

IJU Case Reports
Introduction Desmoid tumors are rare, locally invasive, non‐metastasizing intermediate grade neoplasms. According to the organ procurement and transplantation network report, approximately one million solid organ transplants have been performed globally,
Tsuyoshi Matsuda, Shota Yamada, Ayaka Tsuchiyama, Hiroki Kurata, Yuta Mukae, Shinji Okano, Yasushi Mochizuki, Ryoichi Imamura   +7 more
doaj   +1 more source

An unusual finding in a desmoid-type fibromatosis of the pancreas: a case report and review of the literature

Journal of Medical Case Reports, 2018
Background Desmoid-type fibromatoses are rare benign and fibrous tumors that account for approximately 0.03% of total neoplasms. Within this category of neoplasms, pancreatic desmoid-type fibromatosis is an extremely rare subgroup, accounting for ...
Joseph Clarence Torres, Chen Xin
doaj   +1 more source

UK guidelines for the management of soft tissue sarcomas [PDF]

, 2016
Soft tissue sarcomas (STS) are rare tumours arising in mesenchymal tissues, and can occur almost anywhere in the body. Their rarity, and the heterogeneity of subtype and location means that developing evidence-based guidelines is complicated by the ...
Dangoor, A, Gerrand, C, Grimer, R, Judson, I, Seddon, B, Whelan, J   +5 more
core   +1 more source

Large intra-thoracic desmoid tumor with airway compression: A case report and review of the literature

Journal of Pediatric Surgery Case Reports, 2016
Intra-thoracic desmoid tumors are exceedingly rare tumors in the pediatric population, and can present with compression of cardiopulmonary structures and respiratory compromise. Surgical and anesthetic management of these tumors are challenging.
Tyler D. Robinson, Matias Bruzoni, Peter Than, Safwan Halabi, James Wall   +4 more
doaj   +1 more source

Desmoid Tumor [PDF]

Mayo Clinic Proceedings, 2018
Meryl C, Nath, Michael S, Torbenson, Lori A, Erickson   +2 more
openaire   +2 more sources

Tumor desmoide abdômino-pélvico Abdominopelvic desmoid tumor

Revista Brasileira de Ginecologia e Obstetrícia, 2009
O tumor desmoide é uma neoplasia não capsulada, localmente agressiva, originária dos fibroblastos dos tecidos músculo-aponeuróticos. Embora ele não tenha comportamento maligno, tal como capacidade de gerar metástases ou de invasão, o tumor desmoide tem uma alta capacidade de crescimento local, causando deformidades nos órgãos adjacentes, dor e ...
Fernando Antonio Mourão Valejo, Daniel Guimarães Tiezzi, Gisele Alborguetti Nai   +2 more
openaire   +1 more source