Diagnostic utility of cyclin D1 in the diagnosis of small round blue cell tumors in children and adolescents
Diagnostic utility of cyclin D1 in the diagnosis of small round blue cell tumors in children and adolescents
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DOI:
10.1016/j.humpath.2016.07.038
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发表时间:
2017-02-01
期刊:
影响因子:
3.3
通讯作者:
Parenti, Rosalba
中科院分区:
文献类型:
--
作者:
Magro, Gaetano;Salvatorelli, Lucia;Parenti, Rosalba
Small round blue cell tumors (SRBCTs) of children and adolescents are often diagnostically challenging lesions. With the increasing diagnostic approach based on small biopsies, there is the need of specific immunomarkers that can help in the differential diagnosis among the different tumor histotypes to assure the patient a correct diagnosis for proper treatment. Based on our recent studies showing cyclin D1 overexpression in both Ewing sarcoma/primitive peripheral neuroectodermal tumor (EWS/pPNET) and peripheral neuroblastic tumors (neuroblastoma and ganglioneuroblastoma), we immunohistochemically assessed cyclin D1 immunoreactivity in 128 cases of SRBCTs in children and adolescents to establish its potential utility in the differential diagnosis. All cases of EWS/pPNET and the undifferentiated/poorly differentiated neuroblastomatous component of all peripheral neuroblastic tumors exhibited strong and diffuse nuclear staining (> 50% of neoplastic cells) for cyclin D1. In contrast, this marker was absent from rhabdomyosarcoma (regardless of subtype) and lymphoblastic lymphoma, (either B- or T-cell precursors), whereas it was only focally detected (< 5% of neoplastic cells) in some cases of Wilms tumor (blastemal component) and desmoplastic small round cell tumor. Our findings suggest that cyclin Dl can be exploitable as a diagnostic adjunct to conventional markers in confirming the diagnosis of EWS/pPNET or neuroblastoma/ ganglioneuroblastoma. Its use in routine practice may also be helpful for those cases of SRBCT with undifferentiated morphology that are difficult to diagnose after application of the conventional markers. (C) 2016 Elsevier Inc. All rights reserved.