首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Immature teratoma of the tectum mesencephali with histopathological detection of rudimentary eye anlage in a 3-year-old boy: Report of a rare case
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Immature teratoma of the tectum mesencephali with histopathological detection of rudimentary eye anlage in a 3-year-old boy: Report of a rare case

机译:组织病理学检测3岁男孩中脑盖膜未成熟畸胎瘤:罕见病例报告

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摘要

Intracranial teratoma is a rare neoplasm derived from omnipotent germinal cells that can contain mesoderm, endoderm and/or ectoderm layer tissue. Histologically teratomas are characterized by abnormal structures like teeth or bone that can be further subdivided into mature and immature according to the presence of incompletely differentiated tissue. Characteristic intracranial teratomas are space-occupying lesions in the pineal region and often present with hydrocephalic symptoms due to aqueduct stenosis. A 3-year-old boy presented with a peracute hemiparesis, fatigue and speech deficit. MRI diagnostics showed a cystic, partially solid, inhomogeneous contrast-enhancing formation at the top of the tectum mesencephali with consecutive aqueduct compression. The patient underwent a sub-occipital craniotomy via a supracerebellar approach and complete resection was achieved. The histopathological examination mainly showed mature tissue of ectodermal, mesodermal and endodermal origin. However, small areas of undifferentiated neuroectodermal tissue within an optic vesicle formation were detected, leading to the diagnosis of an immature teratoma. In due course, the patient was discharged in good health without neurological deficits. To our knowledge, optic vesicle-containing intracranial germ cell tumors are extremely rare. Here we report a unique case with immature neuroectodermal tissue within an optic vesicle formation in an otherwise mature teratoma.
机译:颅内畸胎瘤是一种罕见的肿瘤,它来自全能生殖细胞,可以包含中胚层,内胚层和/或外胚层组织。组织学畸胎瘤的特征是异常结构,如牙齿或骨骼,根据不完全分化的组织的存在,可以进一步细分为成熟和不成熟。特征性颅内畸胎瘤是松果体区域占位性病变,由于输水管狭窄而常出现脑积水症状。一个3岁的男孩表现出严重的偏瘫,疲劳和言语障碍。 MRI诊断显示,在中脑顶盖的顶部出现囊性,部分实心的,不均匀的增强造影剂,并连续导水管受压。该患者通过race小脑上入路进行了枕下颅骨开颅手术,并实现了完全切除。组织病理学检查主要显示外胚层,中胚层和内胚层来源的成熟组织。然而,在视神经小泡形成内的未分化神经外胚层组织的小区域被检测到,导致未成熟畸胎瘤的诊断。在适当的时候,该患者身体健康,没有神经功能缺损。据我们所知,含有视泡的颅内生殖细胞肿瘤极为罕见。在这里,我们报告了一个不成熟的神经外胚层组织在否则成熟的畸胎瘤的视泡形成内的独特病例。

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