Results 71 to 80 of about 67,534 (151)

A Rare Case Report on Dedifferentiated Liposarcoma of the Thigh Mimicking an Abscess With Vascular Features: A Diagnostic Challenge With Fatal Outcome

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Dedifferentiated liposarcoma (DDLPS) is an aggressive malignant soft tissue tumor comprising approximately 15%–20% of all liposarcomas. When presenting in the extremities, its atypical clinical and radiological features may mimic vascular or infectious conditions, posing a serious diagnostic challenge that can delay curative intervention. A 60‐
Rashid Shahriar Sazal   +5 more
wiley   +1 more source

Prevalence and Risk Factors for Financial Toxicity Among Sarcoma Patients During and Following Treatment Across the Lifespan

open access: yesCancer 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

Survival and prognostic factors among different types of liposarcomas based on SEER database

open access: yesScientific Reports
The aim of this study is to elucidate the disparities in survival and risk factors among different subtypes of liposarcoma, through analysis of epidemiological and prognostic data.
Jiaqi Zhao   +5 more
doaj   +1 more source

A case of dedifferentiated liposarcoma showing a biphasic pattern on 2-deoxy-2-F18- fluoro-D-glucose positron emission tomography/ computed tomography

open access: yesRare Tumors, 2013
Integrated 2-deoxy-2-F18-fluoro-D-glucose positron emission tomography combined with computed tomography (FDG-PET/CT) has been used in the field of soft tissue sarcoma.
Manabu Hoshi   +4 more
doaj   +1 more source

Pleomorphic liposarcoma of the chest wall: A case report

open access: yes, 2017
Liposarcomas represent the most common type of soft tissue sarcoma. Liposarcoma is sub-classified into dedifferentiated, myxoid, pleomorphic, and unspecified types, with the pleomorphic form being the most rare.
David St. Michel   +4 more
core   +1 more source

Natural Killer Cells in Paediatric Soft Tissue Sarcomas: A Systematic Review

open access: yesPediatric Blood &Cancer, Volume 73, Issue 9, September 2026.
ABSTRACT Paediatric soft tissue sarcomas (pSTS) are a rare and heterogeneous group of malignant tumours arising in tissues of mesenchymal origin. The role of natural killer (NK) cells in pSTS remains poorly understood, with evidence fragmented across small preclinical studies and early‐phase clinical trials.
Raya Dean   +7 more
wiley   +1 more source

Not all NTRK fusions in mesenchymal neoplasia are driver events: implications on classification and targeted therapy

open access: yesThe Journal of Pathology: Clinical Research, Volume 12, Issue 5, September 2026.
Abstract NTRK fusions drive the pathogenesis of a distinctive group of mesenchymal neoplasms with significant impact on classification and targeted therapy. However, unexpected NTRK fusions have been reported in other sarcoma entities, raising uncertainty over their specificity and clinical management.
Mohamed A Yakoub   +4 more
wiley   +1 more source

Myxoid pleomorphic liposarcoma [PDF]

open access: yes
Myxoid pleomorphic liposarcoma (MPL) is an extremely rare adipocytic tumor, recently recognized as a distinct entity in the 5th edition of the World Health Organization (WHO) Classification of Soft Tissue and Bone Tumors.
Dorpe, Jo Van   +4 more
core   +1 more source

Cytodiagnostic features of angiofibroma of soft tissue: A review of 16 cases to identify characteristic findings and their diagnostic significance

open access: yesCancer Cytopathology, Volume 134, Issue 9, September 2026.
Abstract Background Angiofibroma of soft tissue (AFST) is a rare benign fibroblastic/myofibroblastic neoplasm. Despite several published studies describing the clinicopathological features of AFSTs, its cytological characteristics remain poorly documented. This study aimed to identify distinctive cytological features that may support accurate diagnosis.
Takahiko Ito   +10 more
wiley   +1 more source

Renal liposarcoma

open access: yesInternational Brazilian Journal of Urology, 2004
INTRODUCTION: Liposarcoma is a malignant mesenchymal tumor frequently located in retroperitoneum, and rarely presenting an isolated lesion in kidney. CASE REPORT: Female, Caucasian, 49-year old patient, with family history of renal polycystic disease ...
Diogo A.L. Bader   +2 more
doaj   +1 more source

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