Results 81 to 90 of about 18,775 (216)

Histological heterogeneity and distributional difference of gastric carcinosarcoma: report of 4 cases and literature review

open access: yesPolish Journal of Pathology, 2019
Carcinosarcoma is a rare malignant neoplasm, consisting of both epithelial and mesenchymal component. Primary gastric carcinosarcoma is rare and poorly understood.
Ling Nie   +5 more
doaj   +1 more source

METTL3 Increases Temozolomide Resistance in MGMT‐Negative Glioblastoma by Enhancing CBX5 mRNA Stability in an m6A‐IGF2BP2‐Dependent Manner

open access: yesCNS Neuroscience &Therapeutics, Volume 32, Issue 10, October 2026.
METTL3‐dependent m6A modification and IGF2BP2‐associated CBX5 mRNA stabilization help maintain CBX5 expression in MGMT‐negative glioblastoma. During temozolomide (TMZ) treatment, CBX5 contributes to ATM–RAD51‐associated signaling, limits persistent DNA damage and apoptosis, and thereby supports cell survival and TMZ resistance.
Hui Deng   +4 more
wiley   +1 more source

Primary hepatic carcinosarcoma

open access: yes, 2011
BACKGROUND: Primary hepatic carcinosarcoma is a rare malignant tumor containing an intimate mixture of carcinomatous and sarcomatous elements. Reports on risk factors, epidemiology, and pathogenesis of the tumor as well as the experience in its treatment
Mehmet Çelikbilek   +15 more
core   +1 more source

Carcinosarcoma of the biliary tract: Two case reports and a review of the literature

open access: yes, 2005
Carcinosarcoma of the biliary tract is extremely rare. Little is known about the natural course of these tumours, or the best available treatment. We present two cases of carcinosarcoma of the biliary tract, one of the gall bladder and one of the common ...
Read-Jones, SL   +4 more
core   +1 more source

True Carcinosarcoma of the Esophagus: Report of a Case [PDF]

open access: yes, 2008
Carcinosarcoma of the esophagus is a malignant neoplasm involving both carcinomatous and sarcomatous components. We report a patient with true esophageal carcinosarcoma who underwent laparoscopy-assisted surgery.
Kanji Kawachi   +10 more
core   +1 more source

Synchronous endometrial adenocarcinoma and carcinosarcoma in endometrial polyp

open access: yes, 2018
Introduction: Carcinosarcoma is a rare gynecological malignancy and it usually follows an aggressive clinical course. Rarely, it can be confined to an endometrial polyp or be synchronous with another gynecological malignancy.
Qazi Azher   +2 more
core   +2 more sources

Demographic features and prognostic factors of uterine carcinosarcoma: a study at a specialized center in Saudi Arabia

open access: yesFrontiers in Oncology
ObjectivesUterine carcinosarcoma is a rare, aggressive biphasic tumor comprising both carcinomatous and sarcomatous elements. The overall prognosis of women with uterine carcinosarcoma is poor, with a median overall survival of less than two years.
Wala Mehros   +17 more
doaj   +1 more source

Effect of Adjuvant Therapy on Oncologic Outcomes of Surgically Confirmed Stage I Uterine Carcinosarcoma: a Turkish Gynecologic Oncology Study

open access: yesBalkan Medical Journal, 2019
Background: Uterine carcinosarcoma is rare neoplasm that mostly presents as metastatic disease. Stage is one of the most important prognostic factor, however, the management of the early stage uterine carcinosarcoma is still controversial.
Günsu Kimyon Cömert   +16 more
doaj   +1 more source

Carcinosarcoma of minor salivary gland of lower lip with pelvic metastasis: A case report

open access: yesJournal of Craniomaxillofacial Research, 2017
Carcinosarcoma of salivary gland is a rare and aggressive tumor composed of both carcinomatous and sarcomatous components which metastasize together. Most tumors arise in parotid gland from a preexisting pleomorphic adenoma.
Abbas Karimi   +2 more
doaj  

Carcinosarcoma of the vulva: a case report

open access: yes, 2010
Carcinosarcoma is a well-recognized tumor even if it is an uncommon entity. Neoplasms usually occur in the oral cavity, pharynx, esophagus, larynx and skin, and have been rarely documented in the female genital tract.
RESTA, Leonardo   +13 more
core   +1 more source

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