Results 61 to 70 of about 1,192,520 (208)
Surgical Case Reports, 2017 Background Intra-abdominal desmoid tumors, particularly those derived from the stomach, are rare. Such tumors are associated with a history of familial adenomatous polyposis (FAP), trauma, or surgical procedures in general.
Kazushi Miyata +2 more
doaj +1 more source
Clinical and Translational Radiation Oncology, 2021 Desmoid tumors are benign, but may have a locally invasive tendency that commonly results in local recurrence. Most occur on the body trunk or extremities, whereas a head and neck desmoid tumor is relatively rare.
Takuya Sawada +9 more
doaj +1 more source
Cancer Reports, Volume 9, Issue 10, October 2026.ABSTRACT Background Financial toxicity (FT) describes the impact of cancer and treatment‐related financial burden. We evaluated the prevalence and risk factors for FT among sarcoma patients. Methods A sarcoma cohort was constructed to assess health outcomes.
Michael J. Robinson +21 more
wiley +1 more source
Postoperative recurrence of desmoid tumors: clinical and pathological perspectives [PDF]
, 2015 Background: The clinical features and the pathological changes of desmoid tumors were studied to point out the key factors affecting the recurrence. Methods: The clinical data and specimens of 56 patients who underwent desmoid tumor resection from ...
Tang, Shun +13 more
core +1 more source
Desmoid Tumor after Sleeve Gastrectomy: Case Report and Literature Review
GE: Portuguese Journal of Gastroenterology, 2023 Desmoid tumor is a rare mesenchymal neoplasm of unknown etiology. Despite rare, the diagnosis of desmoid tumors after bariatric surgery is increased over the last few years.
Renato Medas +4 more
doaj +1 more source
Neuropathology and Applied Neurobiology, Volume 52, Issue 5, October 2026.We report a case of primary intramedullary infantile fibrosarcoma (IFS) in a 4‐week‐old infant with rapidly progressive cervical myelopathy. Histology showed a spindle cell tumour with diffuse S100 and pan‐TRK expression. RNA sequencing identified an RBPMS::NTRK3 fusion.
Mégane Le Quang +8 more
wiley +1 more source
Annals of Oncology, 2012 Desmoid tumors (DTs) are histologically benign proliferations of stromal cells but may grow locally aggressive. Overall, DTs are rare (0.03% of all neoplasms). A minority of DTs is associated with Gardner syndrome and mutations of the familial adenomatous polyposis (FAP) gene. Most spontaneous DTs are associated with mutations of the beta-catenin gene.
C, Escobar +4 more
openaire +2 more sources
Breast Fibromatosis: Clinical and Pathological Insights From Two Case Reports
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Breast fibromatosis is a benign, locally aggressive spindle‐cell tumor mimicking carcinoma. We report two cases in patients aged 15 and 61 years, highlighting its wide age range. Accurate histopathology prevents overtreatment. Modern management emphasizes individualized care, including active surveillance, complete surgical excision when ...
Vahid Soleimani +2 more
wiley +1 more source
Desmoid tumor of the tongue [PDF]
, 2008 Desmoid tumors are rare neoplasms accounting for 0.03% of all neoplasms and have an estimated incidence of 2 to 4 per million per year. World Health Organization currently refers to all of the deep types of fibromatosis as desmoidtype of fibromatoses ...
Ali, Aiman A., Suresh, Chandra Sekharan
core
Perineurioma‐like EMA‐positive calvarial neoplasms: clinicopathological study of eight cases
Histopathology, Volume 89, Issue 3, Page 544-553, September 2026.Perineurioma‐like, EMA‐positive calvarial neoplasms (PLECN) are a rare group of intraosseous spindle cell tumours that demonstrate overlapping morphologic features of perineurioma and fibroblastic meningioma. These lesions tend to behave indolently but show a propensity for progressive growth.
Raheel Rizwan +9 more
wiley +1 more source