Results 1 to 10 of about 1,080 (118)

Progressive insights into fibrosarcoma diagnosis and treatment: leveraging fusion genes for advancements

open access: yesFrontiers in Cell and Developmental Biology, 2023
Fibrosarcoma, originating from fibroblast cells, represents a malignant neoplasm that can manifest across all genders and age groups. Fusion genes are notably prevalent within the landscape of human cancers, particularly within the subtypes of ...
Xiaodi Tang   +6 more
doaj   +1 more source

DNA aptamer S11e recognizes fibrosarcoma and acts as a tumor suppressor

open access: yesBioactive Materials, 2022
Fibrosarcoma is a serious malignant mesenchymal tumor with strong invasiveness, high recurrence, and poor prognosis. Currently, surgical resection is the main treatment for fibrosarcoma.
Yunyi Liu   +10 more
doaj   +1 more source

Intra Oral Fibrosarcoma with Various Histopathological Patterns: A Rare Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Fibrosarcoma has been defined as a malignant mesenchymal tumour, the cells of which recapitulate the appearance of the normal fibroblast, with variable collagen production. Fibrosarcoma is a very uncommon tumour in the head and neck regions constituting
A. Vikram Simha Reddy   +4 more
doaj   +1 more source

Silencing SAPCD2 Represses Proliferation and Lung Metastasis of Fibrosarcoma by Activating Hippo Signaling Pathway

open access: yesFrontiers in Oncology, 2020
The primary problem associated with fibrosarcoma is its high potential to metastasize to the lung. Aberrant expression of SAPCD2 has been widely reported to be implicated in the progression and metastasis in multiple cancer types.
Bowen Zhu   +10 more
doaj   +1 more source

Fibrosarcoma of the corpus cavernosum: case report and literature review

open access: yesBMC Surgery, 2021
Background Fibrosarcoma is a very rare tumor that arises from fibrous tissue. Less than 5% of fibrosarcoma originate from the urogenital tract. Penile fibrosarcoma, even more rare, is characterized by pain, enlargement, penile erection and urinary tract ...
Ziwei Liu, Wenda Zou
doaj   +1 more source

The Use of Crizotinib in Sclerosing Epithelioid Fibrosarcoma with ALK Mutation: A Case Report

open access: yesCase Reports in Oncology, 2023
Sclerosing epithelioid fibrosarcoma is an ultra-rare and aggressive high-grade fibrosarcoma that was originally described in 1995. More than 100 cases are documented worldwide, with the most extensive case series reporting a high rate of recurrence and ...
Ahmed Badran   +6 more
doaj   +1 more source

Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original

open access: yesBMC Pediatrics, 2023
Background Infantile fibrosarcoma is a rare pediatric soft tissue tumor and usually appears in children before one year of age. Distal extremities constitute the most frequently affected locations, and other tissues such as the trunk, head and neck, gut,
Juan Geng   +6 more
doaj   +1 more source

Ovarian fibrosarcoma : A Case Report

open access: yesAndalas Obstetrics and Gynecology Journal, 2023
This case report aims to report and discuss cases of ovarian fibrosarcoma. Ovarian fibrosarcoma is a rare case that generally occurs in women who have menopause. In the case of ovarian fibrosarcoma, the patient was 43 years old, had two children, and had
Syamel Muhammad, Reyhan Julio
doaj   +1 more source

Neoplasms in domestic hamsters in Southern Brazil: epidemiological and pathological aspects of 40 cases1 [PDF]

open access: yesPesquisa Veterinária Brasileira, 2021
: Although neoplasms are commonly reported in domestic hamsters, retrospective studies approaching spontaneous tumors with data regarding epidemiological findings are scarce.
Maria F. Wentz   +7 more
doaj   +1 more source

Establishment of a Jaw Fibrosarcoma Patient-Derived Xenograft and Evaluation of the Tumor Suppression Efficacy of Plumbagin Against Jaw Fibrosarcoma

open access: yesFrontiers in Oncology, 2020
Background: Head and neck fibrosarcoma is a rare malignant tumor, accounting for about 1% of all head and neck tumors. It can also occur in the jaw bone, for which surgical resection is the main treatment but the recurrence rate is high and the prognosis
Yuqi Xin   +10 more
doaj   +1 more source

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