PMID- 21267687 OWN - NLM STAT- MEDLINE DCOM- 20111220 LR - 20211020 IS - 1532-2807 (Electronic) IS - 1219-4956 (Linking) VI - 17 IP - 3 DP - 2011 Sep TI - The evaluation of CD99 immunoreactivity and EWS/FLI1 translocation by fluorescence in situ hybridization in central PNETs and Ewing's sarcoma family of tumors. PG - 619-25 LID - 10.1007/s12253-010-9358-3 [doi] AB - Ewing's sarcoma family of tumors (ESFTs) are indicated by malignant, small, round and blue cell tumors of the bone and soft tissue. Gene rearrangements between EWS gene on chromosome 22q12 and members of the ETS gene family are common in and specific to ESFTs. Another defining characteristic of ESFTs is their membranous expression of the CD99. In contrast, such translocations and immunoreactivity are not found in central primitive neuroectodermal tumors (cPNETs). The aim of this study was to investigate the detection of EWS/FLI1 translocations and CD99 immunoreactivity in order to evaluate their clinicopathological features and their roles in the differential diagnosis of these tumors. In this study, we investigated CD99 immunoreactivity using immunohistochemistry and Ewing's sarcoma / Friend leukaemia virus integration 1 (EWS/FLI1) translocation using the fluorescence in situ hybridization (FISH) method in 23 cases. CD99 expression was detected in 10/11 (90%) ESFT cases and 2/7 cPNET cases. In 18 cases EWS/FLI1 translocation was examined using the FISH method. The EWS/FLI1 translocations were detected in 7/8 (87.5%) ESFTs cases, whereas non of 8 cPNET cases were detected with this translocation. One case could not be classified as either central or peripheral, showed EWS/FLI1 translocation. There was a statistically significant difference in CD99 expression (p = 0.0013) and EWS/FLI1 translocation (p = 0,002) between cPNETs and ESFTs cases. In conclusion, CD99 expression and EWS/FLI1 translocation are specific and sensitive markers in the diagnosis of ESFTs. However, these were often not found in cases of cPNET. Therefore, in the diagnosis of ESFTs, clinical, radiological, histopathological and immunohistochemical parameters should always be evaluated together. FAU - Vural, Cigdem AU - Vural C AD - Department of Pathology, Baskent University Faculty of Medicine, Ankara, Turkey. dr.cvural@gmail.com FAU - Uluoglu, Omer AU - Uluoglu O FAU - Akyurek, Nalan AU - Akyurek N FAU - Oguz, Aynur AU - Oguz A FAU - Karadeniz, Ceyda AU - Karadeniz C LA - eng PT - Journal Article DEP - 20110126 PL - Switzerland TA - Pathol Oncol Res JT - Pathology oncology research : POR JID - 9706087 RN - 0 (12E7 Antigen) RN - 0 (Antigens, CD) RN - 0 (Biomarkers, Tumor) RN - 0 (CD99 protein, human) RN - 0 (Cell Adhesion Molecules) RN - 0 (EWS-FLI fusion protein) RN - 0 (Oncogene Proteins, Fusion) RN - 0 (Proto-Oncogene Protein c-fli-1) RN - 0 (RNA-Binding Protein EWS) SB - IM MH - 12E7 Antigen MH - Adolescent MH - Adult MH - Antigens, CD/*metabolism MH - Biomarkers, Tumor/genetics/metabolism MH - Bone Neoplasms/genetics/metabolism/pathology MH - Cell Adhesion Molecules/*metabolism MH - Child MH - Child, Preschool MH - Female MH - Follow-Up Studies MH - Humans MH - Immunoenzyme Techniques MH - In Situ Hybridization, Fluorescence MH - Male MH - Neuroectodermal Tumors, Primitive, Peripheral/*genetics/*metabolism/pathology MH - Oncogene Proteins, Fusion/*genetics MH - Prognosis MH - Proto-Oncogene Protein c-fli-1/*genetics MH - RNA-Binding Protein EWS/*genetics MH - Retrospective Studies MH - Sarcoma, Ewing/*genetics/*metabolism/pathology MH - *Translocation, Genetic MH - Young Adult EDAT- 2011/01/27 06:00 MHDA- 2011/12/21 06:00 CRDT- 2011/01/27 06:00 PHST- 2010/05/05 00:00 [received] PHST- 2010/12/29 00:00 [accepted] PHST- 2011/01/27 06:00 [entrez] PHST- 2011/01/27 06:00 [pubmed] PHST- 2011/12/21 06:00 [medline] AID - 10.1007/s12253-010-9358-3 [doi] PST - ppublish SO - Pathol Oncol Res. 2011 Sep;17(3):619-25. doi: 10.1007/s12253-010-9358-3. Epub 2011 Jan 26.