Results 11 to 20 of about 67,534 (151)

Diffuse intra-abdominal sarcomatosis in myxoid pleomorphic liposarcoma. [PDF]

BMJ Case Rep
We 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 ...
Tseng WW, Liang Y, Nguyen B, Agulnik M, Creytens D.   +4 more
europepmc   +3 more sources

Primary Breast Pleomorphic Liposarcoma Evaluation With MRI and Pathology: A Rare Case. [PDF]

Eur J Breast Health, 2023
, Yılmaz R. Primary Breast Pleomorphic Liposarcoma Evaluation With MRI and Pathology: A Rare Case.
Günöz Cömert R, Bayram A, Yılmaz R.
europepmc   +2 more sources

Pleomorphic retroperitoneal liposarcoma with kidney infiltration mimicking renal trauma

Urology Case Reports, 2021
Pleomorphic retroperitoneal liposarcoma are uncommon malignant tumor which hard to treat condition for its local aggressiveness and clinical specificity. A 84 years-old male patient complained with an abdominal mass and left flank pain without hematuria.
Faris El Haq, Sawkar Vijay Pramod, Ferry Safriadi, Bethy S. Hernowo   +3 more
doaj   +2 more sources

Pleomorphic liposarcoma of the foot: a case report [PDF]

Diagnostic Pathology, 2008
Background Liposarcomas are among the most common sarcomas of adult life. Pleomorphic liposarcoma, characterized by pleomorphic lipoblasts, is the rarest subtype. To our knowledge only three cases of pleomorphic liposarcoma of the foot or ankle have been
Orlić Dubravko, Vuletić Lovorka, Jakovčević Antonija, Brčić Luka, Seiwerth Sven   +4 more
doaj   +2 more sources

A Para-Scrotal Pleomorphic Liposarcoma Mimicking As Another Scrotum (Pseudo-Scrotum): A Case Report. [PDF]

Cureus, 2023
Liposarcomas are a subtype of soft tissue sarcomas arising from lipoblasts, a mesenchymal cell lineage that commonly arises from deep tissues of the body.
Jadhav K, Venkateswaran R, Landge R, Kadam A, Rashid R.   +4 more
europepmc   +2 more sources

Primary orbital pleomorphic liposarcoma in a child: A case report [PDF]

American Journal of Ophthalmology Case Reports, 2022
Purpose: To report a rare case of primary orbital pleomorphic liposarcoma and present a relevant literature review. Observations: An 11-year-old boy presented with an enlarging, painless lower right eyelid mass that was noted 4 months ago.
Trakanta Wannapanich, Paitoon Pratipanawat   +1 more
doaj   +2 more sources

Myxoid Pleomorphic Liposarcoma of the Spermatic Cord: A Rare Entity at a Rare Site. [PDF]

Cureus
Myxoid pleomorphic liposarcoma (MPLPS) is an extremely rare entity that has been recognized and included in the literature recently. Liposarcomas are adipocytic tumors that are usually located in the extremities and retroperitoneum.
Chandrasekaran Y, Amitkumar K, Elamaran A, Sudalaimuthu M, Kumaran S.   +4 more
europepmc   +2 more sources

Case report: Pathological complete response to perioperative treatment of radiotherapy combined with angiogenesis inhibitor in a patient with pleomorphic liposarcoma. [PDF]

Front Oncol, 2023
Background Liposarcomas (LPS) are mesenchymal malignancies with four principal subtypes presenting distinct molecular and clinical features. Pleomorphic liposarcoma (PLPS) is one of the rarest and most aggressive subtypes of LPS.
Zhang C, Liu W, Wang B, Zhu N, Guo X, Wang Z, Zhuang R, You Y, Zhang Y, Tong H, Lu W, Zhou Y.   +11 more
europepmc   +2 more sources

Clinical Outcome and Impact of Ayurvedic Rasayana Therapy in Metastatic Pleomorphic Liposarcoma

Indian Journal of Ayurveda and Integrative Medicine KLEU
Pleomorphic liposarcoma is the rarest subtype of liposarcoma, targeting fat cells in the deep soft tissues. It is a high-grade sarcoma of lipogenic origin.
Yogesh Narayan Bendale, Poonam Birari-Gawande, Avinash Kadam   +2 more
doaj   +2 more sources

Myxoid Pleomorphic Liposarcoma: A Review and Update. [PDF]

Cancer Genomics Proteomics
Myxoid 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.
Nishio J, Nakayama S, Aoki M.
europepmc   +2 more sources