نتایج جستجو برای: undifferentiated pleomorphic sarcomas

تعداد نتایج: 21951  

2012
David Roberge Siavosh Vakilian Yazan Z. Alabed Robert E. Turcotte Carolyn R. Freeman Marc Hickeson

Soft-tissue sarcomas spread predominantly to the lung and it is unclear how often FDG-PET scans will detect metastases not already obvious by chest CT scan or clinical examination. Adult limb and body wall soft-tissue sarcoma cases were identified retrospectively. Ewing's sarcoma, rhabdomyosarcoma, GIST, desmoid tumors, visceral tumors, bone tumors, and retroperitoneal sarcomas were excluded as...

2014
Chul-Hwan Kim Jong-Won Jang Moon-Young Kim Yong-Hwan Kim Hang-Gul Kim Joo-Hwan Kim

Undifferentiated pleomorphic sarcoma (UPS), previously known as malignant fibrous histiocytoma, occurs commonly in the soft tissues in adult, but is rare in the maxillofacial region. It consists of undifferentiated mesenchymal tumor cells resembling histiocytes and fibroblasts. The purpose of this article is to report a case of UPS in the mandible. A 44-year-old patient presented with a painful...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2015
Jakob Hofvander Johnbosco Tayebwa Jenny Nilsson Linda Magnusson Otte Brosjö Olle Larsson Fredrik Vult von Steyern Nils Mandahl Christopher D M Fletcher Fredrik Mertens

PURPOSE Undifferentiated pleomorphic sarcoma (UPS) is defined as a sarcoma with cellular pleomorphism and no identifiable line of differentiation. It is typically a high-grade lesion with a metastatic rate of about one third. No tumor-specific rearrangement has been identified, and genetic markers that could be used for treatment stratification are lacking. We performed transcriptome sequencing...

Journal: :Journal of proteome research 2014
Euan Murray Lenka Hernychová Michaela Scigelova Jenny Ho Marta Nekulova John Robert O'Neill Rudolf Nenutil Karel Vesely Sinclair R Dundas Catharine Dhaliwal Hannah Henderson Richard L Hayward Donald M Salter Bořivoj Vojtěšek Ted R Hupp

Sarcomas are rare forms of cancer with a high unmet clinical need that develop in connective tissue, such as muscle, bone, nerves, cartilage, and fat. The outcome for patients is poor, with surgery and postoperative radiotherapy the standard treatment for patients. A better understanding of the molecular pathology of sarcoma may allow for the development of novel therapeutics. There are dozens ...

Journal: :Sarcoma 2008
Josefin Fernebro Ana Carneiro Anders Rydholm Henryk A. Domanski Anna Karlsson Åke Borg Mef Nilbert

Purpose. Patients with soft tissue sarcomas (STS) are at increased risk of second primary malignancies, including a second STS, but distinction between metastases and a second primary STS is difficult. Patients and Methods. Array-based comparative genomic hybridization (aCGH) was applied to 30 multiple STS of the extremities and the trunk wall from 13 patients. Different histotypes were present...

2012
Chang Ye Yale Wang Qingxia Wei Ilkyu Han Shingo Sato Ronak Ghanbari-Azarnier Heather Whetstone Raymond Poon Jiayi Hu Feifei Zheng Phil Zhang Weishi Wang Jay S. Wunder Benjamin A. Alman

Like many solid tumors, sarcomas are heterogeneous and include a small fraction of the so-called side population (SP) cells with stem-like tumor-initiating potential. Here, we report that SP cells from a soft tissue tumor of enigmatic origin termed undifferentiated pleomorphic sarcoma (also known as malignant fibrous histiocytoma or MFH sarcoma) display activation of both the Hedgehog and Notch...

2013
Sara Martoreli Silveira Rolando Rolando Andre Rios Villacis Fabio Albuquerque Marchi Mateus de Camargo Barros Filho Sandra Drigo Linde Cristovam Scapulatempo Neto Isabela Werneck da Cunha Ademar Lopes Silvia Regina Rogatto

Results LMS presented lower frequency of genomic alterations in comparison with UPS. None of the variables were identified as independent prognostic factors, but gains at 1q21.3 were significantly associated with poor survival and showed almost significance as an independent prognostic factor (relative risk 13.8, P = 0.019). In addition, copy number profile of UPS and LMS was indistinguishable ...

2012
Jae Myoung Noh Seung Jae Huh Doo Ho Choi Won Park Seok Jin Nam

We describe two cases of post-radiation sarcoma after breast cancer treatment. The first patient was a 61-year-old woman who underwent partial mastectomy of the right breast and adjuvant whole breast irradiation 7 years previously. Subsequently, a rapidly growing mass from the anterior arc of the right fifth rib was incidentally detected on an abdomino-pelvic computed tomography scan. The secon...

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