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一名5个月大男童的松果体原基肿瘤。

Pineal anlage tumor in a 5-month-old boy.

作者信息

Olaya Joffre E, Raghavan Ravi, Totaro Laura, Zouros Alexander

机构信息

Department of Neurosurgery, Loma Linda University Medical Center, Loma Linda, California 92354, USA.

出版信息

J Neurosurg Pediatr. 2010 Jun;5(6):636-40. doi: 10.3171/2010.2.PEDS09294.

Abstract

Pineal tumors are rare neoplasms that are categorized into pineoblastomas, pineocytomas, and pineal parenchymal tumors of intermediate differentiation. Pineal anlage tumors are primary pineal tumors with neuroepithelial and ectomesenchymal differentiation and without endodermal differentiation. The authors review the literature and report the case of a 5-month-old boy with a pineal anlage tumor. This is only the sixth case of a pineal anlage tumor reported in the English-language literature adding to the understanding of this tumor's presentation, immunomorphological and molecular characteristics, embryological origin, radiological appearance, treatment outcome, and prognosis.

摘要

松果体肿瘤是罕见的肿瘤,分为松果体母细胞瘤、松果体细胞瘤和中间分化的松果体实质肿瘤。松果体原基肿瘤是具有神经上皮和外胚间叶分化且无内胚层分化的原发性松果体肿瘤。作者回顾了文献并报告了一例患有松果体原基肿瘤的5个月大男孩的病例。这是英文文献中报道的第六例松果体原基肿瘤病例,有助于加深对该肿瘤的临床表现、免疫形态学和分子特征、胚胎学起源、放射学表现、治疗结果及预后的了解。

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