Epithelial marker expression does not rule out a diagnosis of Ewing’s sarcoma family of tumours

[1]  C. Antonescu,et al.  EWSR1‐ATF1 fusion is a novel and consistent finding in hyalinizing clear‐cell carcinoma of salivary gland , 2011, Genes, chromosomes & cancer.

[2]  P. Picci,et al.  Molecular diagnosis in Ewing family tumors: the Rizzoli experience--222 consecutive cases in four years. , 2011, The Journal of molecular diagnostics : JMD.

[3]  J. Nishio,et al.  A novel t(4;22)(q31;q12) produces an EWSR1–SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor , 2011, Modern Pathology.

[4]  Antonio Martínez,et al.  The many faces of atypical Ewing’s sarcoma. A true entity mimicking sarcomas, carcinomas and lymphomas , 2011, Virchows Archiv.

[5]  F. Larousserie,et al.  Une tumeur surrénalienne inhabituelle : tumeur d’Ewing , 2011 .

[6]  L. Donner,et al.  CD99-positive large cell neuroendocrine carcinoma with rearranged EWSR1 gene in an infant: a case of prognostically favorable tumor , 2010, Virchows Archiv.

[7]  D. Osuna,et al.  The Clinical Relevance of Molecular Genetics in Soft Tissue Sarcomas , 2010, Advances in anatomic pathology.

[8]  A. D. Dei Tos,et al.  Soft tissue tumors associated with EWSR1 translocation , 2010, Virchows Archiv.

[9]  A. Llombart‐Bosch,et al.  Molecular Diagnosis of Ewing Sarcoma Family of Tumors: A Comparative Analysis of 560 Cases With FISH and RT-PCR , 2009, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

[10]  B. Bjerkehagen,et al.  t(19;22)(q13;q12) Translocation leading to the novel fusion gene EWSR1‐ZNF444 in soft tissue myoepithelial carcinoma , 2009, Genes, chromosomes & cancer.

[11]  A. Llombart‐Bosch,et al.  Histological heterogeneity of Ewing’s sarcoma/PNET: an immunohistochemical analysis of 415 genetically confirmed cases with clinical support , 2009, Virchows Archiv.

[12]  P. Sorensen,et al.  E-cadherin cell-cell adhesion in ewing tumor cells mediates suppression of anoikis through activation of the ErbB4 tyrosine kinase. , 2007, Cancer research.

[13]  J. Goldblum,et al.  Intercellular junctions in Ewing sarcoma/primitive neuroectodermal tumor: additional evidence of epithelial differentiation , 2005, Modern Pathology.

[14]  J. Goldblum,et al.  Morphologic and Immunophenotypic Diversity in Ewing Family Tumors: A Study of 66 Genetically Confirmed Cases , 2005, The American journal of surgical pathology.

[15]  M. Selig,et al.  Keratin-Positive Ewing's Sarcoma: An Ultrastructural Study of 12 Cases , 2005, International journal of surgical pathology.

[16]  R. Sciot,et al.  Cytokeratin-Positive Meningeal Peripheral PNET/Ewing's Sarcoma of the Cervical Spinal Cord: Diagnostic Value of Genetic Analysis , 2005, International journal of surgical pathology.

[17]  A. Llombart‐Bosch,et al.  Electron microscopy and other ancillary techniques in the diagnosis of small round cell tumors. , 2003, Seminars in diagnostic pathology.

[18]  A. Folpe,et al.  Primary Ewing's Sarcoma/Primitive Neuroectodermal Tumor of the Kidney: A Clinicopathologic and Immunohistochemical Analysis of 11 Cases , 2002, The American journal of surgical pathology.

[19]  P. Casali,et al.  Cytokeratin immunoreactivity in 41 cases of ES/PNET confirmed by molecular diagnostic studies. , 2001, The American journal of surgical pathology.

[20]  A. Folpe,et al.  Immunohistochemical Detection of FLI-1 Protein Expression: A Study of 132 Round Cell Tumors With Emphasis on CD99-Positive Mimics of Ewing's Sarcoma/Primitive Neuroectodermal Tumor , 2000, The American journal of surgical pathology.

[21]  A. Folpe,et al.  Clear Cell Myomelanocytic Tumor of the Falciform Ligament/Ligamentum Teres: A Novel Member of the Perivascular Epithelioid Clear Cell Family of Tumors With a Predilection for Children and Young Adults , 2000, The American journal of surgical pathology.

[22]  M. Ladanyi,et al.  Cytokeratin immunoreactivity in Ewing's sarcoma: prevalence in 50 cases confirmed by molecular diagnostic studies. , 2000, The American journal of surgical pathology.

[23]  S. Steinberg,et al.  Neuroectodermal differentiation in Ewing's sarcoma family of tumors does not predict tumor behavior. , 1999, Human pathology.

[24]  J. Davison,et al.  Primary cutaneous Ewing's sarcoma: immunophenotypic and molecular cytogenetic evaluation of five cases. , 1998, The American journal of surgical pathology.

[25]  T. Triche,et al.  Comparison of Ewing's sarcoma of bone and peripheral neuroepithelioma. An immunocytochemical and ultrastructural analysis of two primitive neuroectodermal neoplasms. , 1994, Archives of pathology & laboratory medicine.

[26]  H. Roels,et al.  The immunophenotype of Ewing's sarcoma. An immunohistochemical analysis. , 1993, Pathology, research and practice.

[27]  R. Moll,et al.  Immunocytochemical analysis of Ewing's tumors. Patterns of expression of intermediate filaments and desmosomal proteins indicate cell type heterogeneity and pluripotential differentiation. , 1987, The American journal of pathology.

[28]  V. Lehto,et al.  Histogenesis of Ewing’s sarcoma , 1982, Virchows Archiv. B, Cell pathology including molecular pathology.

[29]  R. Hutter,et al.  Primitive multipotential primary sarcoma of bone , 1966, Cancer.

[30]  O. Delattre,et al.  [An unusual adrenal tumor: Ewing tumor]. , 2011, Annales de pathologie.

[31]  I. Francis,et al.  Soft tissue high grade myoepithelial carcinoma with round cell morphology: report of a newly described entity with EWSR1 gene rearrangement. , 2011, The Gulf journal of oncology.