Results 71 to 80 of about 22,681 (186)

Primary Orbital Myxoid Liposarcoma

, 2023
Although liposarcoma is the most prevalent soft tissue sarcoma in adults, head and neck liposarcomas are rare and account for less than 5% of all liposarcomas. The primary orbital location is even more exceptional, with fewer than 100 cases documented in
Benavides-Huerto, Miguel Armando,, Lagunas-Rangel, Francisco Alejandro,, Moreno-Paramo, Daniel,, Benavides-Huerto, Miguel Armando, Daniel Moreno-Páramo, Francisco Alejandro Lagunas-Rangel, Lagunas-Rangel, Francisco Alejandro, Paramo-Figueroa, Lourdes, Miguel Armando Benavides-Huerto, Lourdes Páramo-Figueroa, Moreno-Paramo, Daniel, Paramo-Figueroa, Lourdes,   +11 more
core   +1 more source

Analysis of MDM2 and TP53 genes in canine liposarcoma

Scientific Reports
Canine liposarcoma is an uncommon tumor that shares morphological similarities with its human counterpart. In dogs, the genetic features of this tumor are unknown and, based on immunohistochemical studies, amplification of the gene MDM2 and the mutation ...
Luisa Vera Muscatello, Dario de Biase, Thais Maloberti, Enrico di Oto, Giovanni Tallini, Valeria Pellegrino, Barbara Bacci, Paola Roccabianca, Elvio Lepri, Luca Crippa, Giancarlo Avallone   +10 more
doaj   +1 more source

Leiomyosarcoma and liposarcoma in young patients: The national netsarc+ network experience

EJC Paediatric Oncology, 2023
Background: Leiomyosarcoma (LMS) and liposarcoma (LPS) are ultra-rare sarcomas in pediatric (0–18 years) and young adult (19−30) populations. We aimed to analyze their clinical characteristics at these young ages and to determine whether they should be ...
Anne-Laure Genevois, Matthieu Carton, Myriam Jean-Denis, Joanna Cyrta, Nadège Corradini, Pablo Berlanga, Claire Chemin-Airiau, Charles Honore, Sophie El Zein, Anne-Sophie Defachelles, Emmanuelle Bompas, Philippe Anract, Justine Gantzer, Marie Karanian, Angélique Rome, Florence Duffaud, Christine Chevreau, Sarah Watson, Axel Le Cesne, Carmen Llacer, François Le Loarer, Gaëlle Pierron, François Gouin, Anne Gomez-Mascard, Sylvain Causeret, Françoise Ducimetière, Elsa Kalbacher, Maud Toulmonde, Jean-Yves Blay, Daniel Orbach   +29 more
doaj   +1 more source

Diagnostic and prognostic gene expression signatures in 177 soft tissue sarcomas: hypoxia-induced transcription profile signifies metastatic potential

BMC Genomics, 2007
Background Soft tissue sarcoma (STS) diagnosis is challenging because of a multitude of histopathological subtypes, different genetic characteristics, and frequent intratumoral pleomorphism. One-third of STS metastasize and current risk-stratification is
Bendahl Pär-Ola, Åkerman Måns, Bjerkehagen Bodil, Berner Jeanne-Marie, Fernebro Josefin, Edén Patrik, Müller Christoph, Namløs Heidi, Francis Princy, Isinger Anna, Rydholm Anders, Myklebost Ola, Nilbert Mef   +12 more
doaj   +1 more source

Diagnostic accuracy of ultrasound-guided core needle biopsy versus incisional biopsy in soft tissue sarcoma: an institutional experience

Scientific Reports, 2021
Core needle biopsy (CNB) is gaining in importance due to its advantages in the matter of patient morbidity, time and cost. Nevertheless, controversies still exist regarding the biopsy technique of choice for the accurate diagnosis of soft tissue sarcoma (
Miroslava Cernakova, Gerhard M. Hobusch, Gabriele Amann, Philipp T. Funovics, Reinhard Windhager, Joannis Panotopoulos   +5 more
doaj   +1 more source

The Identification of Risk Factors in the Development of Wound Healing Complications in Soft Tissue Sarcoma Patients

International Wound Journal, Volume 23, Issue 9, September 2026.
ABSTRACT Wound‐healing complications (WHCs) remain a significant challenge in soft tissue sarcoma (STS) surgery, contributing to increased morbidity, prolonged hospitalisation, and impaired functional outcomes. This study aimed to identify predictors of WHC development in STS patients to improve therapeutic strategies and patient recovery. We conducted
Luisa Kriens, Jendrik Hardes, Wiebke Guder, Nina Engel, Marcel Dudda, Arne Streitbuerger   +5 more
wiley   +1 more source

A contemporary review of myxoid adipocytic tumors

, 2019
Myxoid adipocytic tumors encompass a broad heterogeneous group of benign and malignant adipocytic tumors, which are typically myxoid (e.g. myxoid liposarcoma, lipoblastoma and lipoblastoma-like tumor of the vulva) or may occasionally appear predominantly
Creytens, David
core   +1 more source

[Myxoid liposarcoma and pleomorphic liposarcoma: cyto-histological correlations].

Pathologica, 1989
Myxoid liposarcoma and pleomorphic liposarcoma: cito-histological correlations. A correlative cytologic and histologic study of a myxoid liposarcoma of the shoulder in a 72 year-old man and a pleomorphic liposarcoma observed in the retroperitoneum of a 84 year-old woman, are presented.
Capitanio G, BLANDAMURA, STELLA, Barbazza R, Caldart T, Dalla Palma P.   +4 more
openaire   +2 more sources

Outcome of patients with liposarcoma: A retrospective review over 12 ​Years in a single center

Clinical Surgical Oncology
Background: Liposarcoma is the most common soft tissue sarcoma, which comprises around 20% of soft tissue sarcoma. While diverse therapeutic approaches exist for liposarcoma, the primary goal remains the achievement of effective local disease control ...
Teck Liang Tie, Suryasmi Duski
doaj   +1 more source

Paratesticular Embryonal Rhabdomyosarcoma Masquerading as Epididymitis: A Diagnostic Challenge in Adolescents

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Paratesticular rhabdomyosarcoma is a rare malignancy in children and adolescents that frequently presents diagnostic challenges when mimicking benign inflammatory conditions. We report the case of a 14‐year‐old previously healthy male who presented with acute right scrotal pain and swelling initially diagnosed as epididymo‐orchitis.
Saif Khaled Abdalhadi Azzam, Lina Barhoum Barhoum, Ammir Abuzahra, Alaa Alazzeh, Khader Hassouneh, Nour Aldin K. Fakhory, Mohd Othman Lafi, M. I. Jawabreh Issa, Ibrahim Alzatari, Hamza Zughaier   +9 more
wiley   +1 more source