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1. Full Text A phase 2 trial of R1507, a monoclonal antibody to the insulin‐like growth factor‐1 receptor (IGF‐1R), in patients with recurrent or refractory rhabdomyosarcoma, osteosarcoma, synovial sarcoma, and other soft tissue sarcomas: Results of a Sarcoma Alliance for Research Through Collaboration study
by Pappo, Alberto S and Vassal, Gilles and Crowley, John J and Bolejack, Vanessa and Hogendoorn, Pancras C. W and Chugh, Rashmi and Ladanyi, Marc and Grippo, Joseph F and Dall, Georgina and Staddon, Arthur P and Chawla, Sant P and Maki, Robert G and Araujo, Dejka M and Geoerger, Birgit and Ganjoo, Kristen and Marina, Neyssa and Blay, Jean‐Yves and Schuetze, Scott M and Chow, Warren A and Helman, Lee J
Cancer, ISSN 0008-543X, 08/2014, Volume 120, Issue 16, pp. 2448 - 2456
R1507 is safe and well tolerated but has limited activity in patients with recurrent or refractory bone and soft tissue sarcomas. Additional studies to help... 
SARC | sarcoma | IGF‐1R | insulin‐like growth factor | insulin-like growth factor | IGF-1R | ADVANCED SOLID TUMORS | OPEN-LABEL | MECHANISMS | CANCER | EWING SARCOMA | FAMILY | CIXUTUMUMAB | THERAPY | ONCOLOGY | RESISTANCE | INHIBITOR | Humans | Middle Aged | Sarcoma, Ewing - pathology | Antibodies, Monoclonal - therapeutic use | Treatment Outcome | Bone Neoplasms - immunology | Bone Neoplasms - pathology | Sarcoma, Ewing - drug therapy | Sarcoma, Ewing - immunology | Young Adult | Disease-Free Survival | Adolescent | Receptor, IGF Type 1 - immunology | Aged, 80 and over | Adult | Aged | Bone Neoplasms - drug therapy | Child | Antibodies, Monoclonal - immunology | Complications and side effects | Sarcoma | Patient outcomes | Development and progression | Research | Diagnosis | Insulin-like growth factor 1 | Index Medicus | Abridged Index Medicus
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2. Full Text Recurrent BCOR Internal Tandem Duplication and YWHAE-NUTM2B Fusions in Soft Tissue Undifferentiated Round Cell Sarcoma of Infancy: Overlapping Genetic Features With Clear Cell Sarcoma of Kidney
by Kao, Yu-Chien and Sung, Yun-Shao and Zhang, Lei and Huang, Shih-Chiang and Argani, Pedram and Chung, Catherine T and Graf, Nicole S and Wright, Dale C and Kellie, Stewart J and Agaram, Narasimhan P and Ludwig, Kathrin and Zin, Angelica and Alaggio, Rita and Antonescu, Cristina R
The American Journal of Surgical Pathology, ISSN 0147-5185, 08/2016, Volume 40, Issue 8, pp. 1009 - 1020
Soft tissue undifferentiated round cell sarcoma (URCS) occurring in infants is a heterogenous group of tumors, often lacking known genetic abnormalities. On... 
clear cell sarcoma kidney | YWHAE | small blue round cell tumor | infantile | undifferentiated sarcoma | BCOR ITD | primitive mesenchymal myxoid tumor of infancy | SURGERY | COMPLEX | METASTASIS | PATHOLOGY | EWING-SARCOMA | SIGNATURE | CLINICOPATHOLOGICAL REPORT | TRANSCRIPTOMES | RNA-SEQ | TUMOR STUDY-GROUP | DIFFERENTIATION | POLYCOMB GROUP | Kidney Neoplasms - genetics | Humans | Repressor Proteins - genetics | In Situ Hybridization, Fluorescence | Infant | Male | Proto-Oncogene Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Sarcoma - pathology | DNA Mutational Analysis | Oncogene Proteins, Fusion - genetics | Soft Tissue Neoplasms - pathology | Female | Oncogene Fusion - genetics | Sarcoma - genetics | Infant, Newborn | Soft Tissue Neoplasms - genetics | 14-3-3 Proteins - genetics
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3. Sarcomas
by HaDuong, Josephine H and Martin, Andrew A and Skapek, Stephen X and Mascarenhas, Leo
Pediatric Clinics of North America, ISSN 0031-3955, 02/2015, Volume 62, Issue 1, pp. 179 - 200
Malignant bone tumors (osteosarcoma, Ewing sarcoma) and soft-tissue sarcomas (rhabdomyosarcoma, nonrhabdomyosarcoma) account for approximately 14% of childhood... 
Nonrhabdomyosarcoma | Bone | Ewing's | Osteosarcoma | Rhabdomyosarcoma | Soft-tissue sarcoma | SOFT-TISSUE SARCOMAS | PROGNOSTIC-FACTORS | INTERGROUP RHABDOMYOSARCOMA | NONMETASTATIC EWINGS-SARCOMA | CHILDRENS ONCOLOGY GROUP | PRIMITIVE NEUROECTODERMAL TUMOR | NEOADJUVANT CHEMOTHERAPY | ALVEOLAR RHABDOMYOSARCOMA | PEDIATRICS | HIGH-GRADE OSTEOSARCOMA | STUDY-GROUP PROTOCOLS | Bone Neoplasms - therapy | Humans | Child, Preschool | Combined Modality Therapy | Sarcoma - pathology | Bone Neoplasms - pathology | Child | Sarcoma - therapy
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4. Full Text Late effects of chemotherapy and radiotherapy in osteosarcoma and Ewing sarcoma patients: The Italian Sarcoma Group Experience (1983-2006)
by Longhi, Alessandra and Ferrari, Stefano and Tamburini, Angela and Luksch, Roberto and Fagioli, Franca and Bacci, Gaetano and Ferrari, Cristina
Cancer, ISSN 0008-543X, 10/2012, Volume 118, Issue 20, pp. 5050 - 5059
BACKGROUND: Patients with osteosarcoma and Ewing sarcoma have achieved longer survival over the past decades, but late side effects of chemotherapy and... 
cardiotoxicity | infertility | childhood cancer survivors | bone sarcoma | second malignant neoplasm | ADULT SURVIVORS | LOCALIZED OSTEOSARCOMA | HIGH-DOSE METHOTREXATE | DOXORUBICIN | NONMETASTATIC OSTEOSARCOMA | CHILDHOOD-CANCER SURVIVOR | ADJUVANT | NEOADJUVANT CHEMOTHERAPY | CISPLATIN | ONCOLOGY | EXTREMITY | Osteosarcoma - drug therapy | Follow-Up Studies | Humans | Survivors | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Child, Preschool | Infant | Male | Combined Modality Therapy | Disease Progression | Neoplasms, Second Primary - epidemiology | Sarcoma, Ewing - drug therapy | Young Adult | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Heart Diseases | Adolescent | Adult | Female | Bone Neoplasms - drug therapy | Infertility - epidemiology | Child | Chemotherapy | Usage | Care and treatment | Osteosarcoma | Patient outcomes | Radiotherapy | Ewing's sarcoma | Methods | Cancer | Index Medicus | Abridged Index Medicus
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5. Full Text Ewing's sarcoma
by Balamuth, Naomi J, MD and Womer, Richard B, Dr
Lancet Oncology, The, ISSN 1470-2045, 2010, Volume 11, Issue 2, pp. 184 - 192
Summary Progress in the treatment of Ewing's sarcoma, the second most common bone tumour in children and adolescents, has improved survival from about 10% in... 
Hematology, Oncology and Palliative Medicine | TOTAL-BODY IRRADIATION | INDUCED CELL-DEATH | PRIMITIVE NEUROECTODERMAL TUMOR | STANDARD CHEMOTHERAPY | ONCOLOGY | TERM FOLLOW-UP | THERAPEUTIC TARGET | PHASE-II | GROWTH-FACTOR BINDING-PROTEIN-3 | FACTOR-I RECEPTOR | CHILDRENS ONCOLOGY GROUP | Sarcoma, Ewing - secondary | Sarcoma, Ewing - therapy | Humans | Adolescent | Female | Male | Sarcoma, Ewing - diagnosis | Antineoplastic Agents - therapeutic use | Neoplasm Staging | Child | Sarcoma, Ewing - drug therapy | Tyrosine | Chemotherapy | Cyclophosphamide | Anthracyclines | Etoposide | Ewing's sarcoma | Cancer
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6. Full Text BCOR-CCNB3 Fusion Positive Sarcomas: A Clinicopathologic and Molecular Analysis of 36 Cases With Comparison to Morphologic Spectrum and Clinical Behavior of Other Round Cell Sarcomas
by Kao, Yu-Chien and Owosho, Adepitan A and Sung, Yun-Shao and Zhang, Lei and Fujisawa, Yumi and Lee, Jen-Chieh and Wexler, Leonard and Argani, Pedram and Swanson, David and Dickson, Brendan C and Fletcher, Christopher D.M and Antonescu, Cristina R
The American Journal of Surgical Pathology, ISSN 0147-5185, 05/2018, Volume 42, Issue 5, pp. 604 - 615
BCOR-CCNB3 sarcoma (BCS) is a recently defined genetic entity among undifferentiated round cell sarcomas, which was initially classified as and treated... 
CCNB3 | round cell sarcoma | Ewing sarcoma | BCOR | fusions | SURGERY | PCGF HOMOLOGS | CLEAR-CELL-SARCOMA | HOX GENES | PATHOLOGY | ROUND-CELL | DIFFERENTIATED SYNOVIAL SARCOMA | TUMOR STUDY-GROUP | HISTOLOGIC MIMICS | HUMAN CANCERS | KIDNEY | Immunohistochemistry | Predictive Value of Tests | Sarcoma - secondary | Bone Neoplasms - therapy | Humans | Sarcoma, Ewing - pathology | Child, Preschool | Male | Bone Neoplasms - pathology | Sarcoma - therapy | Young Adult | Cyclin B - genetics | Time Factors | Bone Neoplasms - chemistry | Adult | Female | Bone Neoplasms - genetics | Sarcoma - genetics | Child | Genetic Predisposition to Disease | Biomarkers, Tumor - analysis | Neoplasm Recurrence, Local | Repressor Proteins - genetics | Gene Fusion | In Situ Hybridization, Fluorescence | Proto-Oncogene Proteins - genetics | Treatment Outcome | Disease Progression | Sarcoma - chemistry | Phenotype | Sarcoma, Synovial - genetics | Sequence Analysis, RNA | Adolescent | Biomarkers, Tumor - genetics | Sarcoma, Ewing - genetics | Sarcoma, Synovial - pathology | Development and progression | Genotype | Care and treatment | Gene expression | Health aspects | Ewing's sarcoma
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7. Full Text Safety, pharmacokinetics, and preliminary activity of the anti-IGF-1R antibody figitumumab (CP-751,871) in patients with sarcoma and Ewing's sarcoma: a phase 1 expansion cohort study
by Olmos, David, MD and Postel-Vinay, Sophie, MD and Molife, L Rhoda, MD and Okuno, Scott H, MD and Schuetze, Scott M, MD and Paccagnella, M Luisa, PhD and Batzel, Gretchen N, MD and Yin, Donghua, PhD and Pritchard-Jones, Kathryn, Prof and Judson, Ian, Prof and Worden, Francis P, MD and Gualberto, Antonio, MD and Scurr, Michelle, MD and de Bono, Johann S, Dr and Haluska, Paul, MD
Lancet Oncology, The, ISSN 1470-2045, 2010, Volume 11, Issue 2, pp. 129 - 135
Summary Background Figitumumab is a fully human IgG2 monoclonal antibody targeting the insulin-like growth-factor-1 receptor (IGF-1R). Preclinical data suggest... 
Hematology, Oncology and Palliative Medicine | INSULIN | INHIBITION | ONCOLOGY | CP-751,871 | FACTOR SYSTEM | RECEPTOR | COMBINATION | TUMOR-GROWTH | CANCER | IMATINIB MESYLATE | GROWTH-FACTOR-I | Receptor, IGF Type 1 - antagonists & inhibitors | Humans | Middle Aged | Antibodies, Monoclonal - pharmacokinetics | Antibodies, Monoclonal - therapeutic use | Male | Antineoplastic Agents - therapeutic use | Sarcoma - drug therapy | Sarcoma, Ewing - drug therapy | Young Adult | Adolescent | Receptor, IGF Type 1 - immunology | Adult | Female | Antineoplastic Agents - pharmacokinetics | Child | Immunoglobulins, Intravenous | Cohort Studies | Drugs | Care and treatment | Safety and security measures | Oncology, Experimental | Analysis | Immunoglobulin G | Monoclonal antibodies | Research | Ewing's sarcoma | Cancer
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8. Full Text BCOR-CCNB3 (Ewing-like) Sarcoma: A Clinicopathologic Analysis of 10 Cases, In Comparison With Conventional Ewing Sarcoma
by Puls, Florian and Niblett, Angela and Marland, Gillian and Gaston, Czar Louie L and Douis, Hassan and Mangham, D Chas and Sumathi, Vaiyapuri P and Kindblom, Lars-Gunnar
The American Journal of Surgical Pathology, ISSN 0147-5185, 10/2014, Volume 38, Issue 10, pp. 1307 - 1318
BCOR-CCNB3 fusion transcripts resulting from an X-chromosomal paracentric inversion were recently identified in a series of unclassifiable soft tissue and bone... 
Immunohistochemistry | Ewing sarcoma | Small round cell tumor | Translocation-associated sarcoma | BCOR-CCNB3 sarcoma | RT-PCR | SURGERY | translocation-associated sarcoma | FUSION | PROGNOSTIC-FACTORS | CHONDROSARCOMA | TUMOR | PATHOLOGY | IDENTIFICATION | small round cell tumor | immunohistochemistry | BONE | EXPRESSION | ROUND-CELL SARCOMA | Bone Neoplasms - mortality | Predictive Value of Tests | Translocation, Genetic | Prognosis | Humans | Male | Sarcoma, Ewing - mortality | Bone Neoplasms - pathology | Repressor Proteins - analysis | Cyclin B - genetics | Time Factors | Proto-Oncogene Proteins - analysis | Bone Neoplasms - chemistry | Bone Neoplasms - genetics | Child | Sarcoma, Ewing - chemistry | Bone Neoplasms - diagnosis | Biomarkers, Tumor - analysis | Kaplan-Meier Estimate | Proportional Hazards Models | Repressor Proteins - genetics | Gene Fusion | Proto-Oncogene Proteins - genetics | Sarcoma, Ewing - diagnosis | Reverse Transcriptase Polymerase Chain Reaction | Magnetic Resonance Imaging | Cyclin B - analysis | Sarcoma, Ewing - secondary | Biopsy | Adolescent | Biomarkers, Tumor - genetics | Sarcoma, Ewing - genetics
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9. Full Text A Novel CIC-FOXO4 Gene Fusion in Undifferentiated Small Round Cell Sarcoma: A Genetically Distinct Variant of Ewing-like Sarcoma
by Sugita, Shintaro and Arai, Yasuhito and Tonooka, Akiko and Hama, Natsuko and Totoki, Yasushi and Fujii, Tomoki and Aoyama, Tomoyuki and Asanuma, Hiroko and Tsukahara, Tomohide and Kaya, Mitsunori and Shibata, Tatsuhiro and Hasegawa, Tadashi
The American Journal of Surgical Pathology, ISSN 0147-5185, 11/2014, Volume 38, Issue 11, pp. 1571 - 1576
Differential diagnosis of small round cell sarcomas (SRCSs) grouped under the Ewing sarcoma family of tumors (ESFT) can be a challenging situation for... 
CIC-FOXO4 gene fusion | High-throughput transcriptome sequencing | Desmoplastic stroma | Ewing-like sarcoma | Fluorescence in situ hybridization | fluorescence in situ hybridization | SUBTYPE | SURGERY | TRANSLOCATION | desmoplastic stroma | IN-SITU HYBRIDIZATION | high-throughput transcriptome sequencing | PATHOLOGY | TUMORS | Immunohistochemistry | Predictive Value of Tests | Translocation, Genetic | Neck Muscles - pathology | Humans | Middle Aged | Muscle Neoplasms - pathology | Sarcoma, Ewing - pathology | Male | Bone Neoplasms - pathology | Sarcoma, Small Cell - chemistry | Muscle Neoplasms - therapy | Neoplasm Grading | Muscle Neoplasms - genetics | Sarcoma, Small Cell - genetics | Bone Neoplasms - chemistry | Bone Neoplasms - genetics | Cell Differentiation | Sarcoma, Small Cell - pathology | Diagnosis, Differential | Genetic Predisposition to Disease | Sarcoma, Ewing - chemistry | Neck Muscles - chemistry | Biomarkers, Tumor - analysis | Repressor Proteins - genetics | Sarcoma, Small Cell - therapy | Gene Fusion | In Situ Hybridization, Fluorescence | Transcription Factors - genetics | Phenotype | Muscle Neoplasms - chemistry | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing | Sarcoma, Ewing - genetics
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10. Full Text Diagnostic utility of cyclin D1 in the diagnosis of small round blue cell tumors in children and adolescents: Beware of cyclin D1 expression in clear cell sarcoma of the kidney and CIC-DUX4 fusion–positive sarcomas. Comment on Magro et al. (2016)—reply
by Magro, Gaetano, MD, PhD and Salvatorelli, Lucia, MD and Ludwig, Kathrin, MD and Alaggio, Rita, MD
Human Pathology, ISSN 0046-8177, 2017, Volume 67, pp. 226 - 228
[...]they stated that cyclin D1 is not helpful in differentiating these 2 entities. [...]Creytens et al in their Letter to the Editor underlined that cyclin D1... 
Pathology | PATHOLOGY | Sarcoma, Ewing | Sarcoma, Clear Cell | Cyclin D1 | Child | Humans | Adolescent | Sarcoma | Diagnosis | Teenagers | Morphology | Abdomen | Tumors
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11. Full Text Diagnostic utility of cyclin D1 in the diagnosis of small round blue cell tumors in children and adolescents: Beware of cyclin D1 expression in clear cell sarcoma of the kidney and CIC-DUX4 fusion–positive sarcomas. Comment on Magro et al. (2016)
by Creytens, David, MD, PhD and Ferdinande, Liesbeth, MD, PhD and Van Dorpe, Jo, MD, PhD
Human Pathology, ISSN 0046-8177, 2017, Volume 67, pp. 225 - 226
[...]cyclin D1 immunoreactivity was absent in rhabdomyosarcoma and lymphoblastic lymphoma. [...]this marker was also negative, or only focally positive, in the... 
Pathology | PATHOLOGY | Sarcoma, Ewing | Sarcoma, Clear Cell | Cyclin D1 | Child | Humans | Adolescent | Sarcoma | Diagnosis | Pediatrics | Teenagers | Histopathology | Neuroblastoma | Morphology | Tumors
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12. Full Text Treatment pathway of bone sarcoma in children, adolescents, and young adults
by Reed, Damon R and Hayashi, Masanori and Wagner, Lars and Binitie, Odion and Steppan, Diana A and Brohl, Andrew S and Shinohara, Eric T and Bridge, Julia A and Loeb, David M and Borinstein, Scott C and Isakoff, Michael S
Cancer, ISSN 0008-543X, 06/2017, Volume 123, Issue 12, pp. 2206 - 2218
When pediatric, adolescent, and young adult patients present with a bone sarcoma, treatment decisions, especially after relapse, are complex and require a... 
Ewing sarcoma | pathways | adolescent and young adult (AYA) | chemotherapy | osteosarcoma | pediatric | ADJUVANT CHEMOTHERAPY | HISTOLOGIC RESPONSE | PROGNOSTIC-FACTORS | NONMETASTATIC OSTEOSARCOMA | PHASE-II | HIGH-DOSE IFOSFAMIDE | RANDOMIZED CONTROLLED-TRIAL | REFRACTORY EWING SARCOMA | ONCOLOGY | PEDIATRIC-ONCOLOGY-GROUP | HIGH-GRADE OSTEOSARCOMA | Bone Neoplasms - therapy | Sarcoma, Ewing - therapy | Bone Neoplasms - diagnostic imaging | Humans | Neoplasm Recurrence, Local - therapy | Sarcoma, Ewing - pathology | Patient Care Team | Clinical Trials as Topic | Combined Modality Therapy | Radiotherapy | Sarcoma - pathology | Bone Neoplasms - pathology | Sarcoma - therapy | Sarcoma, Ewing - diagnostic imaging | Young Adult | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Orthopedic Procedures | Clinical Decision-Making | Adolescent | Sarcoma - diagnostic imaging | Child | Osteosarcoma - therapy | Osteosarcoma - diagnostic imaging | Osteosarcoma - pathology | Decision-making | Care and treatment | Young adults | Physicians | Analysis | Practice | Bone tumors | Children | Health aspects | Adolescence | Medical research | Therapy | Sarcoma | Toxicity | Decision making | Medical services | Clinical trials | Decisions | Management | Patients | Literature reviews | Bone cancer | Adults | Teenagers | Bone | Adolescents | Cancer | Index Medicus | Abridged Index Medicus | Review
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13. Full Text CIC-rearranged Sarcomas: A Study of 20 Cases and Comparisons With Ewing Sarcomas
by Yoshida, Akihiko and Goto, Keisuke and Kodaira, Makoto and Kobayashi, Eisuke and Kawamoto, Hiroshi and Mori, Taisuke and Yoshimoto, Seiichi and Endo, Otone and Kodama, Narihito and Kushima, Ryoji and Hiraoka, Nobuyoshi and Motoi, Toru and Kawai, Akira
The American Journal of Surgical Pathology, ISSN 0147-5185, 03/2016, Volume 40, Issue 3, pp. 313 - 323
The CIC gene rearrangement exists in a subset of small round cell sarcomas. As the nosologic relationship of these sarcomas to Ewing sarcomas remains... 
Immunohistochemistry | Ewing sarcoma | Diagnosis | Sarcoma | CIC | SURGERY | sarcoma | CIC-DUX4 TRANSLOCATION | diagnosis | PATHOLOGY | TUMORS | IMMUNOHISTOCHEMICAL MARKER | FAMILY | CIC-FOXO4 GENE FUSION | immunohistochemistry | SCLEROSING EPITHELIOID FIBROSARCOMA | TRANSCRIPTION FACTOR | MALIGNANT MESOTHELIOMA | EXPRESSION | ROUND-CELL SARCOMA | Bone Neoplasms - mortality | Predictive Value of Tests | RNA-Binding Proteins - genetics | Prognosis | Bone Neoplasms - therapy | Sarcoma, Ewing - therapy | Humans | Middle Aged | Sarcoma, Ewing - pathology | Male | Sarcoma, Ewing - mortality | Bone Neoplasms - pathology | Sarcoma - therapy | Young Adult | Sarcoma - mortality | Bone Neoplasms - chemistry | Adult | Female | Bone Neoplasms - genetics | Sarcoma - genetics | Calmodulin-Binding Proteins - genetics | Diagnosis, Differential | Sarcoma, Ewing - chemistry | Kaplan-Meier Estimate | Repressor Proteins - genetics | In Situ Hybridization, Fluorescence | Sarcoma - pathology | Sarcoma - chemistry | Gene Rearrangement | Adolescent | Aged | Biomarkers, Tumor - genetics | Sarcoma, Ewing - genetics | RNA-Binding Protein EWS | Index Medicus
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14. Full Text Synovial Sarcoma
by Palmerini, E and Staals, EL and Alberghini, M and Zanella, L and Ferrari, C and Benassi, MS and Picci, P and Mercuri, M and Bacci, G and Ferrari, S
CANCER, ISSN 0008-543X, 07/2009, Volume 115, Issue 13, pp. 2988 - 2998
BACKGROUND: The optimal treatment for synovial sarcoma remains controversial. Treatment, outcome, and prognostic factors in patients treated in a single... 
ADJUVANT CHEMOTHERAPY | synovial sarcoma | ADULT PATIENTS | EWINGS-SARCOMA | SSX FUSION TYPE | SOFT-TISSUE SARCOMAS | SINGLE INSTITUTION | PROGNOSTIC-FACTORS | prognostic factors | chemotherapy | LOCAL RECURRENCE | ONCOLOGY | radiotherapy | soft tissue sarcoma | RETROSPECTIVE ANALYSIS | MULTIVARIATE-ANALYSIS
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15. Full Text Spindle and Round Cell Sarcoma With EWSR1-PATZ1 Gene Fusion: A Sarcoma With Polyphenotypic Differentiation
by Chougule, Abhijit and Taylor, Martin S and Nardi, Valentina and Chebib, Ivan and Cote, Gregory M and Choy, Edwin and Nielsen, G Petur and Deshpande, Vikram
The American Journal of Surgical Pathology, ISSN 0147-5185, 02/2019, Volume 43, Issue 2, pp. 220 - 228
The evolving classification of round cell sarcomas is driven by molecular alterations. EWSR1-PATZ1 fusion positive spindle and round cell sarcoma is one such... 
EWS | SURGERY | DIAGNOSIS | sarcoma | polyphenotypic differentiation | MARKER | PATHOLOGY | SOFT-TISSUE | EWING SARCOMA | fusion | EWSR1 | TUMOR-SUPPRESSOR | PATZ1
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