نتایج جستجو برای: sarcoma tumors

تعداد نتایج: 244044  

2017
Laura Nordio Sabina Fattori Chiara Giudice

Most canine tumors of the eyelid are tumors generally encountered in the skin. They are most commonly of epithelial origin and benign. In this report, we describe the cases of two sibling Czech wolfdogs presented, one year apart, with a subcutaneous mass involving the left eyelid. Both lesions were histologically consistent with a diagnosis of subcutaneous fibrosarcoma. Immunohistochemical anal...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Kårstein Måseide Rita A Kandel Robert S Bell Charles N Catton Brian O'Sullivan Jay S Wunder Melania Pintilie David Hedley Richard P Hill

PURPOSE Hypoxia is associated with malignant progression and poor outcome in several human tumors, including soft tissue sarcoma. Recent studies have suggested that carbonic anhydrase (CA) IX is an intrinsic marker of hypoxia, and that CA IX correlates with poor prognosis in several types of carcinoma. The aim of this study was to quantify the extent of CA IX expression and to investigate wheth...

2016
Fabian Wolpert Michael A Grotzer Felix Niggli Dieter Zimmermann Elisabeth Rushing Beata Bode-Lesniewska

Modern multimodal treatment has significantly increased survival for patients affected by hematologic malignancies, especially in childhood. Following remission, however, the risk of developing a further malignancy is an important issue. The long-term estimated risk of developing a sarcoma as a secondary malignancy is increased severalfold in comparison to the general population. Ewing's sarcom...

Journal: :Cancer discovery 2014
Brian D Crompton Chip Stewart Amaro Taylor-Weiner Gabriela Alexe Kyle C Kurek Monica L Calicchio Adam Kiezun Scott L Carter Sachet A Shukla Swapnil S Mehta Aaron R Thorner Carmen de Torres Cinzia Lavarino Mariona Suñol Aaron McKenna Andrey Sivachenko Kristian Cibulskis Michael S Lawrence Petar Stojanov Mara Rosenberg Lauren Ambrogio Daniel Auclair Sara Seepo Brendan Blumenstiel Matthew DeFelice Ivan Imaz-Rosshandler Angela Schwarz-Cruz Y Celis Miguel N Rivera Carlos Rodriguez-Galindo Mark D Fleming Todd R Golub Gad Getz Jaume Mora Kimberly Stegmaier

UNLABELLED Pediatric Ewing sarcoma is characterized by the expression of chimeric fusions of EWS and ETS family transcription factors, representing a paradigm for studying cancers driven by transcription factor rearrangements. In this study, we describe the somatic landscape of pediatric Ewing sarcoma. These tumors are among the most genetically normal cancers characterized to date, with only E...

Journal: :Cancer research 1967
A Fefer J L McCoy J P Glynn

X-irradiated (400 R) CBF (BALB/c 9 X C57BL/6 o") FI mice inoculated with BALB/c Moloney sarcoma cells developed more tumors and exhibited fewer tumor regressions than normal CBF controls. Most of the latter and only one of the former produced detectable fluorescent antibody as tested against BALB/c Moloney lymphoma cells. BALB/c Moloney sarcoma cells incubated with spleen cells from C57BL/6 mic...

Journal: :Cancer discovery 2014
Franck Tirode Didier Surdez Xiaotu Ma Matthew Parker Marie Cécile Le Deley Armita Bahrami Zhaojie Zhang Eve Lapouble Sandrine Grossetête-Lalami Michael Rusch Stéphanie Reynaud Thomas Rio-Frio Erin Hedlund Gang Wu Xiang Chen Gaelle Pierron Odile Oberlin Sakina Zaidi Gordon Lemmon Pankaj Gupta Bhavin Vadodaria John Easton Marta Gut Li Ding Elaine R Mardis Richard K Wilson Sheila Shurtleff Valérie Laurence Jean Michon Perrine Marec-Bérard Ivo Gut James Downing Michael Dyer Jinghui Zhang Olivier Delattre

UNLABELLED Ewing sarcoma is a primary bone tumor initiated by EWSR1-ETS gene fusions. To identify secondary genetic lesions that contribute to tumor progression, we performed whole-genome sequencing of 112 Ewing sarcoma samples and matched germline DNA. Overall, Ewing sarcoma tumors had relatively few single-nucleotide variants, indels, structural variants, and copy-number alterations. Apart fr...

Journal: :Rossijskij žurnal detskoj gematologii i onkologii 2021

Primitive myxoid mesenchymal tumor of infancy (PMMTI) is an aggressive with a high rate local recurrence, rare metastasis and poor response to chemotherapy.PMMTI soft-tissue sarcoma that preferentially affects infants. It isolated from the group infantile fibrosarcomas or myofibroblastic tumors. PMMTI differs other tumors in clinical course, morphological features primarily molecular genetic ch...

2015
Nirmalya Chakrabarti Nikhilesh Dewasi Snehasish Das Arghya Bandyopadhyay Nandini Bhaduri

Among the group of small round cell tumors of kidney Ewing's sarcoma/PNET is a very rare entity which has aggressive clinical course. We report a case of renal mass in 24 years old male which was histologically diagnosed as small round cell tumor of kidney. Arrangement of the malignant cell along with vascular network in a filigree pattern was suspicious for a diagnosis of Ewing's sarcoma/PNET ...

2017
Kelechukwu U Okoro Matthew D Roby David C Sane Robert E Budin

Primary cardiac sarcoma is a rare malignant myocardial neoplasm that does not exhibit gender predominance or age predilection. The classification of these tumors includes several subtypes, of which synovial sarcoma is a rare manifestation. When present, these tumors portend a poor prognosis with high morbidity and mortality that is attributable to their inherent infiltrative capacity, especiall...

2005
Helen Nadel

Nuclear Medicine examinations are integral in the management of children with cancer. Imaging with conventional gamma camera systems, hybrid gamma camera systems and radiopharmaceuticals; and with positron emission tomography (PET) and PET/ CT systems and positron emitters can be used for staging, metastatic work-up, surveillance follow-up, therapeutic response assessment and treatment. Tumors ...

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