外周髓样上皮瘤:一种罕见的肿瘤。

IF 0.6 Q4 ONCOLOGY

Case Reports in Oncological Medicine Pub Date : 2020-06-26 eCollection Date: 2020-01-01 DOI:10.1155/2020/6817407

W Matrane, S Cherkaoui, M Regragui, N Bennani Guebessi, M Karkouri, S Salam, A Madani, A Quessar, N Khoubila

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引用次数: 1

摘要

根据世界卫生组织，髓样上皮瘤属于胚胎性肿瘤实体。它是一种非常罕见的高度恶性肿瘤，通常影响婴儿和幼儿。通常，肿瘤发生在眼睛或中枢神经系统;在没有确定的治疗方法的情况下，很少有外周位置的报道。识别和区分这种肿瘤与其他鉴别肿瘤是必要的，以便更好地了解其生物学和确定最佳治疗方法。本文报告一例3岁女童的异位盆腔内髓样上皮瘤伴肝转移。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Peripheral Medulloepithelioma: A Rare Entity to Know.

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Peripheral Medulloepithelioma: A Rare Entity to Know.

According to the World Health Organization, medulloepithelioma belongs to the embryonal neoplasm entity. It is a very rare, highly malignant tumor typically affecting infants and young children. Usually, the tumor arises in the eye or in the central nervous system; a peripheral location has been rarely reported without an established treatment. The recognition and separation of this neoplasm from other differential tumors are mandatory for better understanding of its biology and determination of optimal treatment. This paper reports a case of an ectopic intrapelvic medulloepithelioma with liver metastasis in a 3-year-old girl.

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来源期刊

Case Reports in Oncological Medicine ONCOLOGY-

自引率

0.00%

发文量

审稿时长

16 weeks

期刊介绍： Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.