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dc.contributor.authorComunoglu, Cem
dc.contributor.authorOCAK, SÜHEYLA
dc.contributor.authorÖZCAN, RAHŞAN
dc.contributor.authorComunoglu, Nil
dc.date.accessioned2022-07-04T16:01:27Z
dc.date.available2022-07-04T16:01:27Z
dc.identifier.citationComunoglu N., Comunoglu C., ÖZCAN R., OCAK S., "Ewing Sarcoma Displaying Extensive Well Differentiated Neuroblastomatous Differentiation: A Case Report", FETAL AND PEDIATRIC PATHOLOGY, 2022
dc.identifier.issn1551-3815
dc.identifier.othervv_1032021
dc.identifier.otherav_ceb07297-174e-4bc4-8771-4d3f49466922
dc.identifier.urihttp://hdl.handle.net/20.500.12627/184760
dc.identifier.urihttps://doi.org/10.1080/15513815.2022.2072420
dc.description.abstractIntroduction A tumor with EWSR1/FLI fusion displaying extensive well differentiated neuroblastomatous differentiation is presented. Case report A nine-year-old female patient had a thoracic vertebra 8 paraspinal mass. The lesion was resected incompletely. Histopathologically, a small round cell tumor with gangliomatous differentiation was seen. This was initially diagnosed as an intermixed ganglioneuroblastoma. In the completion surgery biopsy material, the small round cell component was more prominent. Immunohistochemistry for both samples showed membrane positivity for CD99 and nuclear positivity for NKX2.2 in the small round cell component of the tumor. Molecular analysis revealed EWSR1/FLI fusion. The diagnosis then considered a "Ewing Sarcoma Displaying Extensive Well Differentiated Neuroblastomatous Differentiation". Conclusion Tumors with the EWSR1/FLI fusion may show neuroblastomatous differentiation. We chose to treat this as an Ewing Sarcoma (ES). Recognition of this phenomenon in ES cases may prevent a possible misinterpretation and a failure in oncologic treatment.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectHistology
dc.subjectPediatrics
dc.subjectPathology and Forensic Medicine
dc.subjectKlinik Tıp (MED)
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectHealth Sciences
dc.subjectBiochemistry (medical)
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectBiyoloji ve Biyokimya
dc.subjectPATOLOJİ
dc.titleEwing Sarcoma Displaying Extensive Well Differentiated Neuroblastomatous Differentiation: A Case Report
dc.typeMakale
dc.relation.journalFETAL AND PEDIATRIC PATHOLOGY
dc.contributor.departmentİstanbul Üniversitesi , Cerrahpaşa Tıp Fakültesi , Tıbbi Patoloji
dc.contributor.firstauthorID3422169


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