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Sclerosing epithelioid fibrosarcoma as a rare cause of ascites in a young man: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2008
Introduction Sclerosing epithelioid fibrosarcoma is a rare but distinct variant of fibrosarcoma that not only presents as a deep-seated mass on the limbs and neck but can also occur adjacent to the fascia or peritoneum, as well as the trunk and spine. We
Smith Philip J   +3 more
doaj   +4 more sources

Diagnostic challenges and laparoscopic management of mitotically active cellular fibroma of the ovary: a case report and literature review [PDF]

open access: yesFrontiers in Oncology
Mitotically active cellular fibroma (MACF) is a rare ovarian neoplasm characterized by mild to moderate cytological atypia and increased mitotic activity, often presenting diagnostic challenges due to its overlap with ovarian fibrosarcoma.
Shuxu Tian   +5 more
doaj   +2 more sources

Histological and Immunohistochemical Findings of an Extremely Rare Multi‐Organ Metastasis of Fibrosarcoma in a Holstein Cow [PDF]

open access: yesVeterinary Medicine and Science
Introduction Fibrosarcomas are most frequently encountered in senior dogs and cats, but they have also been documented in various other species such as alpacas, llamas, ferrets, cows, sheep, goats and horses.
Abdolrasoul Namjou   +4 more
doaj   +2 more sources

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

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