Results 41 to 50 of about 67,534 (151)

An extremely rare case of recurrent pleomorphic myxoidliposarcoma with response to eribulin chemotherapy – A case report

Rare Tumors, 2023
Pleomorphic myxoid liposarcoma (PML) is a newly recognized entity with aggressive clinical behavior and a tendency to recur. It has histological features of both myxoid and pleomorphic liposarcoma and lacks the molecular and structural chromosomal ...
Raghavendra Rao, Sameer Rastogi, Divya Kashyap, Shamim A Shamim, Adarsh Barwad   +4 more
doaj   +1 more source

Myxoid pleomorphic liposarcoma is distinguished from other liposarcomas by widespread loss of heterozygosity and significantly worse overall survival: a genomic and clinicopathologic study

Modern Pathology, 2022
Myxoid pleomorphic liposarcoma (MPLPS) is a recently described and extremely rare subtype of liposarcoma with a predilection for the mediastinum. However, the genomic features of MPLPS remain poorly understood.
J. Dermawan, Sinchun Hwang, L. Wexler, W. Tap, S. Singer, Chad M. Vanderbilt, C. Antonescu   +6 more
semanticscholar   +1 more source

The Rapidly Expanding Group of RB1-Deleted Soft Tissue Tumors: An Updated Review

Diagnostics, 2021
The classification of soft tissue tumors has evolved considerably in the last decade, largely due to advances in understanding the pathogenetic basis of many of these, sometimes rare, tumors.
Sasha Libbrecht, Jo Van Dorpe, David Creytens   +2 more
doaj   +1 more source

Liposarcoma of stomach: report of a case [PDF]

, 1968
A report is made on a case of liposarcoma of stomach in a 42 year old man. This is the first case of liposarcoma of stomach reported in Japan. The patient has remained asymptomatic for five years after operation.
Orita, Kunzo, Takagi, Shigeru, Kokumai, Yoshiaki, Kawahara, Toru, Kawada, Koichi   +4 more
core   +1 more source

Late widespread skeletal metastases from myxoid liposarcoma detected by MRI only [PDF]

, 2008
Background Myxoid liposarcoma is the second most commonly occurring sub-type of liposarcomas. In contrast to other soft tissue sarcomas, it is known to have a tendency to spread toward extrapulmonary sites, such as soft tissues, retroperitoneum, and the
Lee A David, Lee Bayliss, Bayliss, L, Briggs, TW, David Lee A, O'Donnell Paul, Briggs Timothy WR, Judson, IR, Qureshi, YA, Paul O'Donnell, Judson Ian R, Ian R Judson, Yassar A Qureshi, Bayliss Lee, Timothy WR Briggs, Hanna, SA, Qureshi Yassar A, Sammy A Hanna, O'Donnell, P, Hanna Sammy A, David, LA   +20 more
core   +1 more source

Pleomorphic liposarcoma, case report [PDF]

, 2017
Introducción: El liposarcoma pleomórfico es el subtipo con mayor malignidad, presenta recurrencia local de 37% y metástasis en 10 años de 41%, porcentaje que aumenta directamente con el tamaño de la lesión; además, presenta una supervivencia a los 10 ...
Lubinus Badillo, Federico Guillermo, Ramírez Pedroza, Laura Vanessa, Mantilla Viviescas, Karen Andrea   +2 more
core   +1 more source

Late-onset meningeal metastases in liposarcoma: A case report and review of the literature [PDF]

, 2006
Intracranial metastases from liposarcoma are rare and almost always preceded by the development of systemic tumour spread. We report here a case of liposarcoma with spread to the cranial nervous system 23 years after treatment of the primary tumour.
White, J., Cowie, F., Ferguson, M., Stewart, W.   +3 more
core   +1 more source

Pleomorphic liposarcoma of bone: a rare primary malignant bone tumour [PDF]

, 2018
Background Liposarcoma is an extremely rare primary bone sarcoma. Case presentation We report a case of primary pleomorphic liposarcoma that arose in an 18 year old male in the metaphysis of the left tibia.
S. Wilson, Kastrenopoulou, A., Oppermann, U., Bradley, K., C. McCarthy, Athanasou, N. A., N. A. Athanasou, K. Bradley, Tiemeier, G. L., S. E. Pratap, Gibbons, C. L. M. H., G. L. Tiemeier, Brown, J. M., McCarthy, C., C. L. M. H. Gibbons, J. M. Brown, Pratap, S. E., Z. Orosz, A. Kastrenopoulou, Wilson, S., U. Oppermann, Orosz, Z.   +21 more
core   +3 more sources

Comprehensive genomic profiling of a unique liposarcoma arising in a patient with Li–Fraumeni syndrome and the novel detection of c-myc amplification: a case report

Diagnostic Pathology, 2022
Background Germline TP53 mutations have been frequently reported in patients with Li–Fraumeni syndrome (LFS), resulting in a predisposition to various malignancies.
Hirofumi Watanabe, Fumiyoshi Fujishima, Toru Motoi, Yayoi Aoyama, Tetsuya Niihori, Masanobu Takahashi, Sho Umegaki, Hisashi Oishi, Hiroshi Tada, Ryo Ichinohasama, Hironobu Sasano   +10 more
doaj   +1 more source

Rare aggressive behavior of MDM2-amplified retroperitoneal dedifferentiated liposarcoma, with brain, lung and subcutaneous metastases

Rare Tumors, 2016
Dedifferentiated liposarcoma (DDL) is a histologically pleomorphic sarcoma, traditionally defined as well-differentiated liposarcoma with abrupt transition to high grade, nonlipogenic sarcoma.
Imen Ben Salha, Shane Zaidi, Jonathan Noujaim, Aisha B. Miah, Cyril Fisher, Robin L. Jones, Khin Thway   +6 more
doaj   +1 more source