Mengide Juan Pablo, Jaimovich Sebastián G, Lubieniecki Fabiana J, Rugilo Carlos, Lamas Gabriela, Mantese Beatriz
Neurosurgery Department, Pediatric Hospital "Prof. Dr. Juan P. Garrahan", Buenos Aires, Argentina.
Pathology Department, Pediatric Hospital "Prof. Dr. Juan P. Garrahan", Buenos Aires, Argentina.
Childs Nerv Syst. 2020 Mar;36(3):469-475. doi: 10.1007/s00381-019-04476-7. Epub 2020 Jan 3.
Melanotic neuroectodermal tumor of infancy is a rare neoplasm mainly seen in children under 1 year of life. The most common location of the tumor is the maxilla followed by the cranial vault. Surgery is the treatment of choice and outcome mainly depends on extent of resection.
To report an atypical case of an 8-year-old patient with a melanotic neuroectodermal tumor of infancy, to review the cases with melanotic neuroectodermal tumor of infancy arising from the skull published over the last 13 years, and to provide a diagnostic approach that may allow recognition of a pattern in these rare neoplastic lesions.
A case is reported with a description of the clinical, radiological, surgical, and histopathological features. Additionally, the literature was reviewed to identify reports of patients with melanotic neuroectodermal tumor of infancy arising from the cranial vault and all cases published in PubMed over the last 13 years were included. Only studies that evaluated clinical, radiological, surgical, and histopathological findings were included.
Melanotic neuroectodermal tumor of infancy is a rare entity that may present with unusual features, but nevertheless has an identifiable pattern that allows the tumor to be considered in the differential diagnosis of intracranial space-occupying lesions in children.
婴儿黑色素性神经外胚层肿瘤是一种罕见的肿瘤,主要见于1岁以下儿童。该肿瘤最常见的部位是上颌骨,其次是颅顶。手术是首选治疗方法,其预后主要取决于切除范围。
报告一例8岁婴儿黑色素性神经外胚层肿瘤的非典型病例,回顾过去13年发表的起源于颅骨的婴儿黑色素性神经外胚层肿瘤病例,并提供一种诊断方法,以便在这些罕见的肿瘤性病变中识别出一种模式。
报告一例病例,并描述其临床、放射学、手术和组织病理学特征。此外,对文献进行了回顾,以确定起源于颅顶的婴儿黑色素性神经外胚层肿瘤患者的报告,并纳入过去13年在PubMed上发表的所有病例。仅纳入评估临床、放射学、手术和组织病理学结果的研究。
婴儿黑色素性神经外胚层肿瘤是一种罕见的疾病,可能表现出不寻常的特征,但仍有可识别的模式,这使得该肿瘤可在儿童颅内占位性病变的鉴别诊断中予以考虑。