Results 111 to 120 of about 22,681 (186)

Solitary pancreatic metastasis of extremity myxoid liposarcoma: a case report and literature review

, 2018
Background Myxoid liposarcoma has a distinct migration aptitude; however, pancreatic metastasis is rare. Case presentation We report on the case of a 40-year-old female patient who suffered solitary pancreatic metastasis of myxoid liposarcoma and had a ...
Jian Yu, Jie Wu, Honggang Liu, Dingding Wang, Hong Zhang   +4 more
core   +1 more source

Adipose and Myxoid Tumors of Childhood and Adolescence

, 2012
Adipose and myxoid tumors in children are an unusual and challenging group of neoplasms that have some unique aspects in contrast to these tumors in adults. Less than 10% of soft tissue neoplasms in the 1st 2 decades of life have an adipose phenotype and
ALAGGIO, RITA, Cheryl M. Coffin
core   +1 more source

Clinical presentation, management and outcome of 11132 patients with liposarcoma: a population-based study from the NETSARC+ registryResearch in context

The Lancet Regional Health. Europe
Summary: Background: Liposarcomas (LPS) are among the most common sarcomas, but gather a diversity of rare to ultrarare molecular subtypes whose presentations and natural histories are partially characterized.
Jean-Yves Blay, Maud Toulmonde, Thibaud Valentin, Nelly Firmin, Sarah Watson, Florence Duffaud, Emmanuelle Bompas, Maria Rios, Mikael Ropars, Philippe Anract, Armelle Dufresne, Justine Gantzer, Louis-Romée Le Nail, Esma Saada, Alice Hervieu, Francois Bertucci, Pascale Dubray-Longeras, Vincent Crenn, Christophe Perrin, Pauline Soibinet, Benjamin Verret, Antoine Italiano, Gauthier Decanter, Gwenael Ferron, Sebastien Carrere, Sylvie Bonvalot, Mehdi Brahmi, Clemence Henon, Mariella Spalato-Ceruso, Loic Lebellec, Anne Ducassou, Julien Colard-Thomas, Sophie Piperno-Neumann, Jean-Camille Mattei, Francois Gouin, Mathieu Faron, Thomas Ryckewaert, Pierre Meeus, Charles Honoré, François Le Loarer, Jean-Michel Coindre, Carine Ngo, Alexandra Meurgey, Marie Karanian, Claire Chemin-Airiau, Françoise Ducimetiere, Magali Morelle, Nicolas Penel, Axel Le Cesne   +48 more
doaj   +1 more source

Primary myxoid liposarcoma of the supraglottic larynx

, 2010
Sarcomas are a rare occurrence accounting for roughly 1% of all cancer cases reported. Of these, 9–18% will be identified as liposarcoma. Overall, only 4–9% of all liposarcomas occur in the head and neck region.
Jean Paul Font, Cecilia G Clement, Michael P Underbrink, David M Gleinser, Basim S Mohammed   +4 more
core   +1 more source

Myxoid Liposarcoma of the Spermatic Cord

, 2005
The myxoid liposarcoma, a rare form of spermatic cord liposarcoma, is a neoplasia of adult men which arise from adipose tissue, with a slow and subdolous growth, showing good prognosis and low incidence of local or distant recurrence.
D. Masala, G. Perugia, D. Di Viccaro, M. Liberti, L. Iaboni, S. Teodonio   +5 more
core   +1 more source

Myxoid pleomorphic liposarcoma

, 2020
Joachim Feger, Arlene Campos
openaire   +1 more source

Correlation of magnetic resonance imaging morphological features and diffusion-weighted imaging to soft tissue sarcoma grading

The Egyptian Journal of Radiology and Nuclear Medicine
Background Soft tissue sarcomas (STSs) are a diverse group of rare malignant diseases, with over 50 histologic subtypes and a significant mortality rate.
Aya Mohamed Bassam Hashem, Jihad Badr Metwally, Mohamed Samy Saeid El Azab, Basma Mohamed Abdelhamid Alkalaawy, Rania Zeitoun   +4 more
doaj   +1 more source

Perineal myxoid liposarcoma: report of a case and literature review [PDF]

, 2010
Liposarcomas are rare soft tissue tumour, with an incidence of 30 cases per million population. The myxoid liposarcoma (MLS) consists of 45 – 55% of these tumours, making it the most common subtype. MLS commonly involves the thigh and retroperitoneum but
Mat Hassan, Mohd. Zailani, Mohd Yusof, Mubarak, Ramasamy, Prabhu, Md Nor, Azmi, Harun, Norra   +4 more
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Pleomorphic Liposarcoma Revisited

, 2023
Pleomorphic liposarcoma (PLPS) is the rarest and more aggressive subtype of liposarcomas, accounting for 10% of all liposarcomas. The diagnosis should be considered after the detection of multivacuolated pleomorphic lipoblasts in biopsy specimens.
Tsukamoto, S., Hadjimichael, A.C., Bekos, A., Mavrogenis, A.F., Nitta, Y., Righi, A., Errani, C.   +6 more
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