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[一例多组织病理学类型多中心胶质瘤的尸检病例]

[An autopsy case of multicentric glioma of multiple histopathology].

作者信息

Nakase H, Hisanaga M, Iwanaga H

机构信息

Department of Neurosurgery, National Senboku Hospital, Osaka, Japan.

出版信息

No Shinkei Geka. 1987 Oct;15(10):1073-7.

PMID:3323931
Abstract

An autopsy case is described of an 66-year-old man with multicentric glioma of multiple histopathology, i.e. protoplasmic astrocytoma and glioblastoma. Enhanced CT scan revealed three separate lesions in the right cerebral hemisphere, pons, and cerebellar vermis. Initial diagnosis by CT included metastatic and primary brain tumor, multiple abscess, fungal infection, parasites, tuberculoma, and so on. Biopsy of the right frontal mass revealed astrocytoma grade-2. An autopsy revealed gelatinous, clear marginal mass in the right frontal, parietooccipital and cerebellar vermis; an opaque marginal mass with necrosis in dorsal pons was found. At microscopic examination, the right frontal tumor exhibited continuity with both the paraventricular and the right parietooccipital tumor. The right cerebral hemisphere and cerebellar vermis tumors showed protoplasmic astrocytoma; the dorsal pons tumor showed glioblastoma. CSF examination revealed no tumor cells. Tumor invasion of the internal capsule and the meninges was also not found. Accordingly, we diagnosed as multicentric astrocytoma of multiple histopathology. Only 11 case reports of multicentric glioma were recorded in Japan; only one of which was of multiple histopathology. Worldwide, only 7 case reports of multicentric glioma of multiple histopathology were recorded; this is the first case of protoplasmic astrocytoma and glioblastoma. Seen in terms of pathogenesis of multicentric glioma, this case is thought to be very interesting.

摘要

本文描述了一例66岁男性多中心胶质瘤的尸检病例,该肿瘤具有多种组织病理学类型,即原浆性星形细胞瘤和胶质母细胞瘤。增强CT扫描显示右侧大脑半球、脑桥和小脑蚓部有三个独立病灶。CT初步诊断包括转移性和原发性脑肿瘤、多发性脓肿、真菌感染、寄生虫、结核瘤等。右侧额叶肿块活检显示为2级星形细胞瘤。尸检发现右侧额叶、顶枕部和小脑蚓部有胶冻状、边界清晰的肿块;脑桥背侧有一个边界不清、伴有坏死的肿块。显微镜检查显示,右侧额叶肿瘤与脑室旁及右侧顶枕部肿瘤相连。右侧大脑半球和小脑蚓部肿瘤表现为原浆性星形细胞瘤;脑桥背侧肿瘤为胶质母细胞瘤。脑脊液检查未发现肿瘤细胞。也未发现肿瘤侵犯内囊和脑膜。因此,我们诊断为多组织病理学类型的多中心星形细胞瘤。在日本仅记录了11例多中心胶质瘤病例报告;其中只有1例是多组织病理学类型。在全球范围内,仅记录了7例多组织病理学类型的多中心胶质瘤病例报告;这是首例原浆性星形细胞瘤和胶质母细胞瘤病例。从多中心胶质瘤的发病机制来看,该病例被认为非常有趣。

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