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Modern Pathology, ISSN 0893-3952, 10/2011, Volume 24, Issue 10, pp. 1320 - 1326
Journal Article
Modern Pathology, ISSN 0893-3952, 05/2004, Volume 17, Issue 5, pp. 547 - 552
FLI-1 nuclear transcription factor has been proposed as a useful tool in the differential diagnosis of small round cell sarcomas. Recently, FLI-1 has been... 
Immunohistochemistry | Vascular tumors | FLI-1 | Round cell tumors | EWINGS-SARCOMA | LYMPHOMA KINASE ALK | FUSION TRANSCRIPT | PATHOLOGY | SARCOMA/PRIMITIVE NEUROECTODERMAL TUMOR | vascular tumors | round cell tumors | GENE | DIFFERENTIATED SYNOVIAL SARCOMA | INFLAMMATORY MYOFIBROBLASTIC TUMOR | immunohistochemistry | TRANSCRIPTION FACTOR | CD99 | EWS/FLI | Hemangiosarcoma - metabolism | Proto-Oncogene Protein c-fli-1 | Sarcoma, Kaposi - metabolism | Humans | Lung Neoplasms - metabolism | Rhabdomyosarcoma - metabolism | Sarcoma, Ewing - pathology | Rhabdomyosarcoma - pathology | Trans-Activators - analysis | DNA-Binding Proteins - analysis | Lung Neoplasms - pathology | Colonic Neoplasms - metabolism | Breast Neoplasms - metabolism | Hemangioendothelioma - pathology | Hemangioendothelioma - metabolism | Trans-Activators - immunology | Melanoma - metabolism | Hemangiosarcoma - pathology | Diagnosis, Differential | Sarcoma, Ewing - metabolism | DNA-Binding Proteins - immunology | Carcinoma, Small Cell - metabolism | Sarcoma, Synovial - metabolism | Antibodies, Monoclonal | Melanoma - pathology | Sarcoma - pathology | Sarcoma, Kaposi - pathology | Sarcoma - metabolism | Breast Neoplasms - pathology | Colonic Neoplasms - pathology | Carcinoma, Merkel Cell - metabolism | Carcinoma, Small Cell - pathology | Sarcoma, Synovial - pathology | Carcinoma, Merkel Cell - pathology | Index Medicus
Journal Article
Human Pathology, ISSN 0046-8177, 2016, Volume 60, pp. 58 - 65
Small round blue cell tumors (SRBCTs) of children and adolescents are often diagnostically challenging lesions. With the increasing diagnostic approach based... 
Pathology | Immunohistochemistry | Children | Small round blue cell tumors | Cyclin D1 | Adolescents | Cyclin Dl | FUSION | PATHOLOGY | CANCER | NEUROBLASTIC TUMORS | PRIMITIVE NEUROECTODERMAL TUMOR | PITFALL | ROLES | SARCOMA | KIDNEY | EXPRESSION | Neuroectodermal Tumors, Primitive, Peripheral - pathology | Predictive Value of Tests | Humans | Sarcoma, Ewing - pathology | Child, Preschool | Rhabdomyosarcoma - pathology | Infant | Male | Ganglioneuroblastoma - chemistry | Kidney Neoplasms - chemistry | Bone Neoplasms - pathology | Desmoplastic Small Round Cell Tumor - chemistry | Young Adult | Cyclin D1 - analysis | Precursor Cell Lymphoblastic Leukemia-Lymphoma - metabolism | Desmoplastic Small Round Cell Tumor - pathology | Bone Neoplasms - chemistry | Female | Cell Differentiation | Retrospective Studies | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | Child | Neuroblastoma - pathology | Diagnosis, Differential | Sarcoma, Ewing - chemistry | Neuroblastoma - chemistry | Neuroectodermal Tumors, Primitive, Peripheral - chemistry | Biomarkers, Tumor - analysis | Wilms Tumor - pathology | Biopsy | Adolescent | Kidney Neoplasms - pathology | Rhabdomyosarcoma - chemistry | Wilms Tumor - chemistry | Ganglioneuroblastoma - pathology | T cells | Lymphomas | Diagnosis | Medical colleges | Studies | Ethics | Pediatrics | Archives & records | Morphology | Cell cycle | Teenagers | Neuroblastoma | Tumors | Index Medicus
Journal Article
Modern Pathology, ISSN 0893-3952, 09/2002, Volume 15, Issue 9, pp. 931 - 938
Abnormalities of chromosome 2p23 with expression of ALK1 and p80 occur in both inflammatory myofibroblastic tumor (IMT) and anaplastic large cell lymphoma.... 
ALK gene rearrangements | Anaplastic large cell lymphoma | ALK immunohistochemistry | Inflammatory myofibroblastic tumor | DIAGNOSIS | P80(NPM/ALK) | inflammatory myofibroblastic tumor | INVOLVEMENT | 2P23 | PSEUDOTUMOR | LARGE-CELL LYMPHOMA | TPM3-ALK | PATHOLOGY | GENE | SARCOMAS | anaplastic large cell lymphoma | Immunohistochemistry | Humans | Rhabdomyosarcoma - metabolism | Leiomyosarcoma - metabolism | Rhabdomyosarcoma - pathology | Fibrosarcoma - metabolism | Activin Receptors, Type I - biosynthesis | Chromosomes, Human, Pair 2 - genetics | Protein-Tyrosine Kinases - genetics | Fibrosarcoma - pathology | Neoplasms, Muscle Tissue - metabolism | Nerve Sheath Neoplasms - pathology | Histiocytoma, Benign Fibrous - pathology | Leiomyosarcoma - genetics | Child | Soft Tissue Neoplasms - genetics | Neoplasms, Muscle Tissue - pathology | Histiocytoma, Benign Fibrous - genetics | Diagnosis, Differential | Nerve Sheath Neoplasms - genetics | Leiomyosarcoma - pathology | Histiocytoma, Benign Fibrous - metabolism | Carrier Proteins - biosynthesis | Soft Tissue Neoplasms - metabolism | In Situ Hybridization, Fluorescence | Myofibromatosis - metabolism | Nerve Sheath Neoplasms - metabolism | Fibroma - genetics | Myofibromatosis - genetics | Receptor Protein-Tyrosine Kinases | Fibroma - pathology | Bacterial Proteins | Neoplasms, Muscle Tissue - genetics | Fibrosarcoma - genetics | Membrane Proteins - biosynthesis | Activin Receptors, Type II | Fibroma - metabolism | Chromosome Aberrations | Soft Tissue Neoplasms - pathology | Mesoderm - metabolism | Rhabdomyosarcoma - genetics | Mesoderm - pathology | Myofibromatosis - pathology | Index Medicus
Journal Article
American Journal of Surgical Pathology, ISSN 0147-5185, 05/2009, Volume 33, Issue 5, pp. 705 - 719
The authors present a series of 24 malignant neoplasms arising in preexisting benign spiradenoma, (20), cylindroma (2), and spiradenocylindroma (2). Nineteen... 
Cylindroma | Myoepithelial cells | Basal cell adenocarcinoma | Spiradenoma | Carcinosarcoma | Rhabdomyosarcoma | Brooke-Spiegler syndrome | Spiradenocylindroma | Salivary gland | Malignant | CYLD gene | TRANSFORMATION | SURGERY | carcinosarcoma | cylindroma | myoepithelial cells | CUTANEOUS CYLINDROMAS | spiradenoma | basal cell adenocarcinoma | PATHOLOGY | malignant | DERMAL CYLINDROMAS | TUMORS | salivary gland | ADNEXAL CARCINOMA | MULTIPLE FAMILIAL TRICHOEPITHELIOMA | spiradenocylindroma | ECCRINE SPIRADENOMA | SKIN | rhabdomyosarcoma | Carcinoma, Adenoid Cystic - therapy | Immunohistochemistry | Adenocarcinoma - pathology | Deubiquitinating Enzyme CYLD | Adenoma - genetics | Salivary Gland Neoplasms - genetics | Carcinoma, Squamous Cell - pathology | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Carcinoma, Skin Appendage - pathology | Male | Sarcoma - therapy | Neoplasms, Multiple Primary - therapy | Adenoma - therapy | Tumor Suppressor Proteins - genetics | Aged, 80 and over | Adult | Female | Cell Differentiation | Sarcoma - genetics | Carcinoma - pathology | Soft Tissue Neoplasms - genetics | Soft Tissue Neoplasms - therapy | Neoplasms, Multiple Primary - genetics | Carcinoma, Adenoid Cystic - pathology | Neoplasm Invasiveness | Europe | Treatment Outcome | Neoplasms, Multiple Primary - pathology | Sarcoma - pathology | Syndrome | Metaplasia | Carcinoma, Adenoid Cystic - genetics | Salivary Gland Neoplasms - therapy | Chromosomes, Human, Pair 16 | Soft Tissue Neoplasms - pathology | Adenoma - pathology | Carcinoma - genetics | Carcinoma - therapy | South Africa | Aged | Mutation | Australia | Salivary Gland Neoplasms - pathology | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 8, pp. e20294 - e20294
Journal Article
Cancer, ISSN 0008-543X, 10/2017, Volume 123, Issue 19, pp. 3807 - 3815
This is the first study to systematically interrogate programmed death‐ligand 1 expression in a large series of pediatric cancers. A high frequency of the... 
checkpoint | neuroblastoma | tumor‐infiltrating lymphocytes | programmed death 1/programmed death 1 ligand (PD‐1/PD‐L1) blockade | immunotherapy | pediatric cancer | tumor-infiltrating lymphocytes | programmed death 1/programmed death 1 ligand (PD-1/PD-L1) blockade | ONCOLOGY-GROUP | PD-L1 EXPRESSION | INFILTRATING LYMPHOCYTES | WILMS-TUMOR | UNTREATED MELANOMA | LUNG-CANCER | ONCOLOGY | NEUROECTODERMAL TUMOR | ADULT GLIOBLASTOMA | T-CELLS | CLINICAL-SIGNIFICANCE | Immunohistochemistry | Bone Neoplasms - mortality | Tissue Array Analysis | Humans | Sarcoma, Ewing - pathology | Rhabdomyosarcoma - pathology | Neuroblastoma - mortality | Osteosarcoma - chemistry | Macrophages | Bone Neoplasms - pathology | Burkitt Lymphoma - pathology | Neoplasms - chemistry | Lymphocytes, Tumor-Infiltrating | Burkitt Lymphoma - immunology | Neuroblastoma - immunology | Bone Neoplasms - chemistry | Glioblastoma - chemistry | Child | Neuroblastoma - pathology | Rhabdomyosarcoma - immunology | Sarcoma, Ewing - chemistry | Neuroblastoma - chemistry | Neoplasms - mortality | Bone Neoplasms - immunology | Burkitt Lymphoma - chemistry | Sarcoma, Ewing - immunology | Osteosarcoma - immunology | Glioblastoma - immunology | Neoplasms - immunology | Glioblastoma - pathology | Neoplasm Proteins - analysis | B7-H1 Antigen - analysis | Rhabdomyosarcoma - chemistry | Neoplasms - pathology | Osteosarcoma - pathology | Chemotherapy | Usage | Care and treatment | Diagnosis | Research | Gene expression | Cancer in children | Cancer | Pediatrics | Parkinson's disease | PD-1 protein | Glioblastoma | Neuroblastoma | Tissues | Anticancer properties | Metastases | Lymphocytes | Bioindicators | Children | Movement disorders | Immune response | Neurodegenerative diseases | Tumor cells | Mortality | Patients | Survival | Glioblastoma multiforme | Lymphoma | Burkitt's lymphoma | Immune systems | PD-L1 protein | Biomarkers | Ligands | Death | Antitumor activity | Infiltration | Lymphomas | Diagnostic systems | Tumors | Apoptosis | Index Medicus | Abridged Index Medicus
Journal Article
Pediatric and Developmental Pathology, ISSN 1093-5266, 3/2019, Volume 22, Issue 2, pp. 91 - 97
William A (Bill) Newton Jr practiced pediatric pathology and hematology/oncology at Children’s Hospital of Columbus, Ohio, for over 40 years starting in 1952.... 
William A (Bill) Newton Jr | Intergroup Rhabdomyosarcoma Study | cooperative cancer research | pediatric pathology | neuroblastoma | tumor banking | pediatric hematology-oncology | rhabdomyosarcoma | history of medicine | Wolf Zuelzer | INTERGROUP RHABDOMYOSARCOMA | CYCLOPHOSPHAMIDE | PANCREAS | CLASSIFICATION | PATHOLOGY | TUMORS | PROVISION | THERAPY | SARCOMAS | DISEASE | PEDIATRICS | Index Medicus
Journal Article
World Neurosurgery, ISSN 1878-8750, 01/2018, Volume 109, pp. 1 - 9
Journal Article
Journal Article