Malignant gastrointestinal neuroectodermal tumor as a second malignancy following Ewing sarcoma: Diagnostic pitfalls in the EWSR1‐rearranged tumor spectrum

医学 恶性肿瘤 癌症 肉瘤 病理 内科学
作者
Pierre Khneisser,Mohamed Amine Bani,Sophie Cotteret,Nizar Labaied,Charles Honoré,Gregory Guimard,Pablo Berlanga,Jean‐Yves Scoazec
出处
期刊:Pediatric Blood & Cancer [Wiley]
卷期号:70 (9)
标识
DOI:10.1002/pbc.30438
摘要

Pediatric Blood & CancerEarly View e30438 LETTER TO THE EDITOR Malignant gastrointestinal neuroectodermal tumor as a second malignancy following Ewing sarcoma: Diagnostic pitfalls in the EWSR1-rearranged tumor spectrum Pierre Khneisser, Pierre Khneisser orcid.org/0000-0002-2422-2121 Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorMohamed-Amine Bani, Mohamed-Amine Bani Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorSophie Cotteret, Sophie Cotteret Department of Tumor Genetics, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorNizar Labaied, Nizar Labaied Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorCharles Honore, Charles Honore Department of Surgery, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorGregory Guimard, Gregory Guimard Department of Pediatrics, CHU, Reims, FranceSearch for more papers by this authorPablo Berlanga, Pablo Berlanga orcid.org/0000-0003-1110-7789 Department of Pediatric Oncology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorJean-Yves Scoazec, Corresponding Author Jean-Yves Scoazec [email protected] orcid.org/0000-0003-1604-6823 Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, France Faculté de Médecine, Université Paris Saclay, Le Kremlin-Bicêtre, France Correspondence Jean-Yves Scoazec, Department of Pathology, Gustave Roussy, 114 rue Edouard Vaillant, 94805 Villejuif cedex, France. Email: [email protected]Search for more papers by this author Pierre Khneisser, Pierre Khneisser orcid.org/0000-0002-2422-2121 Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorMohamed-Amine Bani, Mohamed-Amine Bani Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorSophie Cotteret, Sophie Cotteret Department of Tumor Genetics, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorNizar Labaied, Nizar Labaied Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorCharles Honore, Charles Honore Department of Surgery, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorGregory Guimard, Gregory Guimard Department of Pediatrics, CHU, Reims, FranceSearch for more papers by this authorPablo Berlanga, Pablo Berlanga orcid.org/0000-0003-1110-7789 Department of Pediatric Oncology, Gustave Roussy Cancer Campus, Villejuif, FranceSearch for more papers by this authorJean-Yves Scoazec, Corresponding Author Jean-Yves Scoazec [email protected] orcid.org/0000-0003-1604-6823 Department of Pathology, Gustave Roussy Cancer Campus, Villejuif, France Faculté de Médecine, Université Paris Saclay, Le Kremlin-Bicêtre, France Correspondence Jean-Yves Scoazec, Department of Pathology, Gustave Roussy, 114 rue Edouard Vaillant, 94805 Villejuif cedex, France. Email: [email protected]Search for more papers by this author First published: 17 May 2023 https://doi.org/10.1002/pbc.30438Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL REFERENCES 1Stockman DL, Miettinen M, Suster S, et al. Malignant gastrointestinal neuroectodermal tumor: clinicopathologic, immunohistochemical, ultrastructural, and molecular analysis of 16 cases with a reappraisal of clear cell sarcoma-like tumors of the gastrointestinal tract. Am J Surg Pathol. 2012; 36: 857- 868. 2Wang J, Thway K. Clear cell sarcoma-like tumor of the gastrointestinal tract: an evolving entity. Arch Pathol Lab Med. 2015; 139: 407- 412. 3Green C, Spagnolo DV, Robbins PD, Fermoyle S, Wong DD. Clear cell sarcoma of the gastrointestinal tract and malignant gastrointestinal neuroectodermal tumour: distinct or related entities? A review. Pathology. 2018; 50: 490- 498. 4Chang B, Yu L, Guo WW, et al. Malignant gastrointestinal neuroectodermal tumor: clinicopathologic, immunohistochemical, and molecular analysis of 19 cases. Am J Surg Pathol. 2020; 44: 456- 466. 5Kandler T, Cortez E, Clinton L, et al. A case series of metastatic malignant gastrointestinal neuroectodermal tumors and comprehensive genomic profiling analysis of 20 cases. Curr Oncol. 2022; 29: 1279- 1297. 6Flucke U, van Noesel MM, Siozopoulou V, et al. EWSR1 - the most common rearranged gene in soft tissue lesions, which also occurs in different bone lesions: an updated review. Diagnostics (Basel). 2021; 11: 1093. 7Li R, Cao J, Chen L, et al. Malignant gastrointestinal neuroectodermal tumors: clinicopathological and prognostic features of 96 patients. Onco Targets Ther. 2020; 13: 9731- 9740. 8Insabato L, Guadagno E, Natella V, et al. An unusual association of malignant gastrointestinal neuroectodermal tumor (clear cell sarcoma-like) and Ewing sarcoma. Pathol Res Pract. 2015; 211: 688- 692. 9Balkaransingh P, Saad SA, Govil SC, Thind PK, Ballance CM, Weiss AR. Clear cell sarcoma of the gastrointestinal tract presenting as a second malignant neoplasm following neuroblastoma in infancy. Pediatr Blood Cancer. 2012; 58: 481- 482. 10Yang JC, Chou AJ, Oeffinger KC, La Quaglia MP, Wolden SL. Clear cell sarcoma of the gastrointestinal tract after very low-dose therapeutic radiation therapy: a case report. J Pediat Surg. 2012; 47: 1943- 1945. 11Thway K, Judson I, Fisher C. Clear cell sarcoma-like tumor of the gastrointestinal tract, presenting as a second malignancy after childhood hepatoblastoma. Case Rep Med. 2014; 2014:984369. 12Libertini M, Thway K, Noujaim J, et al. Clear cell sarcoma-like tumor of the gastrointestinal tract: clinical outcome and pathologic features of a molecularly characterized tertiary center case series. Anticancer Res. 2018; 38: 1479- 1483. 13Zhan MN, Yu J, Luo RK, Hou YY. Malignant gastrointestinal neuroectodermal tumor, presenting as a second malignancy after gastric adenocarcinoma: a case report and literature review. J Gastrointest Oncol. 2019; 10: 1144- 1150. 14Zambrano E, Reyes-Mugica M, Franchi A, Rosai J. An osteoclast-rich tumor of the gastrointestinal tract with features resembling clear cell sarcoma of soft parts: reports of 6 cases of a GIST simulator. Int J Surg Pathol. 2003; 11: 75- 81. 15Venkataraman G, Quinn AM, Williams J, Hammadeh R. Clear cell sarcoma of the small bowel: a potential pitfall. Case report. APMIS. 2005; 113: 716- 719. Early ViewOnline Version of Record before inclusion in an issuee30438 ReferencesRelatedInformation
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