ASKIN’S TUMOR: A CASE REPORT AND LITERATURE REVIEW

Kiran Bhaisare, Jessica Tellis, Pramod Toshniwal
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Abstract

Askin tumour is an uncommon form of malignant neoplasm that develops from the soft tissues of the thoracopulmonary wall and has a neuroectodermal origin and possess aggressive behavior. As it mimics other common pediatric disorders such as empyema, tuberculosis, lymphoma, rhabdomyosarcoma and neuroblastoma, it acts as a great diagnostic and therapeutic challenge to the treating clinicians. Its rarity, however, contributes greatly to the absence of standardized treatment protocols further facilitating detrimental prognosis. So, the major deciding factor of its survival rate is early and precise diagnosis followed by its treatment. The present study reports a case Askin’s tumor in a child which is locally aggressive and quite rare. While making the definitive diagnosis of an Askin’s tumour of the thorcopulmonary region the possibility of the occurrence of other primitive neuroectodermal tumors (PNET) was not ruled out.
阿金氏肿瘤:病例报告和文献综述
阿斯金瘤是一种不常见的恶性肿瘤,它发生于胸肺壁软组织,起源于神经外胚层,具有侵袭性。由于它与其他常见的儿科疾病(如肺水肿、肺结核、淋巴瘤、横纹肌肉瘤和神经母细胞瘤)相似,因此对临床医生的诊断和治疗提出了巨大挑战。然而,它的罕见性在很大程度上导致了标准化治疗方案的缺失,进一步助长了不利的预后。因此,其存活率的主要决定因素是早期精确诊断和治疗。本研究报告了一例阿斯金氏瘤患儿,该肿瘤具有局部侵袭性,相当罕见。在明确诊断为胸肺区阿斯金氏瘤的同时,也不排除发生其他原始神经外胚层肿瘤(PNET)的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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