Results 41 to 50 of about 20,071 (176)

Spindle Cell Lesions of the Breast: A 12‐Year Experience

open access: yesANZ Journal of Surgery, EarlyView.
This 12‐year, single‐centre study examined 30 core‐biopsy‐diagnosed breast spindle cell lesions (BrSCL), classified as atypical (ASCL, n = 10) or bland (BSCL, n = 20). Following excision, 80% of ASCLs proved malignant, comprising sarcoma, malignant phyllodes tumour and metaplastic carcinoma.
Shalvin Jassal   +4 more
wiley   +1 more source

Bone: Angiosarcoma [PDF]

open access: yes, 2009
Review on Bone: Angiosarcoma, with data on clinics, and the genes ...
Bovée, JVMG, Verbeke, SLJ
core   +1 more source

Multifocal Epithelioid Hemangioma With FOSB Overexpression

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Epithelioid hemangioma (EH) is a benign vascular tumor that most commonly arises on the skin but may also occur in other anatomical locations, including deep soft tissue, bone, visceral organs, penis, and mucosal sites. A hallmark of EH is overexpression of FOS and FOSB, often resulting from various gene fusions.
Phuong Daniels   +6 more
wiley   +1 more source

Clinicopathological characteristics and survival outcomes in patients with angiosarcoma of breast

open access: yesCancer Medicine, 2023
Background Angiosarcoma of the breast is a rare malignancy. There are little data evaluating the survival and estimating the prognostic factors. The best surgical management and the role of systemic adjuvant therapy remain ill‐defined.
Junfeng Li   +6 more
doaj   +1 more source

Angiosarcoma arising in a vagal schwannoma - Report and literature review [PDF]

open access: yes
Schwannoma and angiosarcoma are rare occurrences. Angiosarcoma\u27s occurrence in a preexisting schwannoma is a very rare event with only fifteen cases reported in the literature. We report the sixteenth case of angiosarcoma arising in a schwannoma, a 30-
Naseem, Paras   +9 more
core   +1 more source

Diethylnitrosamine (DENA) recapitulates formation of hepatic angiosarcoma in pigs.

open access: yesPLoS ONE, 2019
Background & aimPrimary hepatic angiosarcoma is a rare tumor with poor prognosis. The aim of this study was to generate a new angiosarcoma model to improve research on hepatic angiosarcoma.MethodsPigs sus scrofa were treated with different regimens of ...
Sonja M Kessler   +10 more
doaj   +1 more source

Loss of TSC1 in secondary angiosarcoma of the breast

open access: yesClinical Case Reports, 2023
Key Clinical Message Post‐radiation angiosarcoma of the breast is a rare complication associated with a poor prognosis. This case reports the first loss of function mutation in TSC1 in breast radiation‐induced angiosarcoma and illustrates the utility of ...
Lucy Rose   +3 more
doaj   +1 more source

Evaluating Fine Needle Aspiration Cytology for Diagnostics of Soft Tissue and Bone Tumours

open access: yesCytopathology, EarlyView.
Systematic comparison of needle aspiration cytology and histopathology for 503 tumours in soft tissue and bone showed high concordance (positive predictive value 94%–100%, negative predictive value 83%–89%). In this original study, the authors show that FNAC is a safe and non‐invasive method for diagnosing suspected sarcomas, with the main objective to
Amanda Husu   +3 more
wiley   +1 more source

IL-13/IL-13Rα2 axis promotes proliferation of angiosarcoma cells

open access: yesScientific Reports
Angiosarcoma is a rare and aggressive soft tissue sarcoma with a poor prognosis and limited treatment options. The role of interleukin-13 (IL-13) and its receptors in angiosarcoma pathogenesis has been largely unknown.
Hinako Saito   +8 more
doaj   +1 more source

Cardiac angiosarcoma with multiple pulmonary metastases: A case report and literature review

open access: yesRadiology Case Reports, 2023
In this report, we describe a 42-year-old man with dyspnea and recurrent hemoptysis who was diagnosed with cardiac angiosarcoma and multiple pulmonary metastases. Before visiting our hospital, he had been misdiagnosed with a lung infection. Bronchoscopy,
Enqi Zhao, MB   +5 more
doaj   +1 more source

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