Beyond the benign: A rare case report of myxoid pleomorphic liposarcoma [PDF]
Radiology Case ReportsMyxoid pleomorphic liposarcoma is a rare and aggressive subtype of soft tissue sarcomas (STS). It primarily arises from adipose tissue and exhibits a high rate of recurrence and metastatic potential.
Rana Uzair Ahmad +2 more
exaly +6 more sources
Eribulin and sintilimab combined with radiotherapy in a heavily pretreated patient with advanced retroperitoneal myxoid pleomorphic liposarcoma: a case report and literature review [PDF]
Frontiers in OncologyMyxoid pleomorphic liposarcoma (MPLPS) is an ultra-rare subtype of soft tissue sarcoma. The limited number of reported cases has led to significant challenges in its clinical management.
Yang Fu, Yaotiao Deng, Dongna Li
exaly +7 more sources
Histopathological Features of Myxoid Pleomorphic Liposarcoma in an African Pygmy Hedgehog (Atelerix Albiventris) [PDF]
Veterinary Sciences, 2022 Myxoid pleomorphic liposarcoma is characterized by pathological features of both pleomorphic liposarcoma and myxoid liposarcoma, as the name suggests. In this case, a myxoid pleomorphic liposarcoma was observed in a 5-year-old male African pygmy hedgehog.
Eun-Joo Lee, Kyu-Shik Jeong
doaj +4 more sources
A rare case of myxoid pleomorphic liposarcoma in an infant: A report [PDF]
International Journal of Surgery Case Reports, 2021 Abstract Introduction and importance MPL (myxoid pleomorphic liposarcoma) is an uncommon type of liposarcoma that affects mostly children and infants. Its aggressive behavior and tendency to recur warrant complete excision despite the challenges of troublesome locations.
Shreya Shrivastav +2 more
exaly +4 more sources
Myxoid pleomorphic liposarcoma is distinguished from other liposarcomas by widespread loss of heterozygosity and significantly worse overall survival: a genomic and clinicopathologic study [PDF]
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. We performed comprehensive genomic profiling of MPLPS in comparison with pleomorphic liposarcoma (PLPS) and myxoid/round cell liposarcoma ...
William D Tap +2 more
exaly +4 more sources
Myxoid pleomorphic liposarcoma in the teres minor muscle: A case report. [PDF]
Medicine (Baltimore), 2022 Rationale: Myxoid pleomorphic liposarcoma (MPL) is a rare aggressive adipocytic tumor that mainly presents in children and adolescents. It is most frequently observed in the mediastinum and rarely in the head and neck, perineal region, or back. Herein, we report the first published case of MPL of the teres minor muscle.
Choi JH +5 more
europepmc +3 more sources
Myxoid pleomorphic liposarcoma of the falciform ligament: a rare case report. [PDF]
J Surg Case Rep, 2022 Abstract Liposarcomas are a group of malignancies that mainly affect adults. Myxoid pleomorphic liposarcoma (MPL) is a newly added subtype of liposarcomas [1]. It is extremely rare and mostly affects infants and children, and it has a predilection for the mediastinum.
AlObaid B +3 more
europepmc +3 more sources
Myxoid Pleomorphic Liposarcoma: A Review and Update. [PDF]
Cancer Genomics ProteomicsMyxoid pleomorphic liposarcoma (MPLPS) is an exceedingly rare and recently recognized adipocytic neoplasm that primarily occurs in children and young adults and shows a strong predilection for the mediastinum. Clinically, MPLPS demonstrates aggressive behavior and exhibits a high propensity for systemic spread and a worse overall survival.
Nishio J, Nakayama S, Aoki M.
europepmc +4 more sources
Acquired isolated factor VII deficiency in a patient with myxoid pleomorphic liposarcoma, case report. [PDF]
Medicine (Baltimore), 2023 Introduction: Acquired factor VII (FVII) deficiency is a rare condition with various causes, including acquired inhibitors to FVII, liver disease, and malignancies. Myxoid pleomorphic liposarcoma is a rare and aggressive form of soft tissue sarcoma that can cause a range of clinical manifestations, including bleeding and ...
Aljabry M +5 more
europepmc +3 more sources
Diffuse intra-abdominal sarcomatosis in myxoid pleomorphic liposarcoma. [PDF]
BMJ Case RepWe present a case of an extremely rare type of soft-tissue sarcoma with an atypical clinical presentation. The patient, a female in her 20s with Li Fraumeni syndrome, had prior surgery for a large intra-abdominal tumour that was given the diagnosis of malignant myxoid spindle cell neoplasm.
Tseng WW +4 more
europepmc +5 more sources