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[恶性小脑节细胞胶质瘤。一例病例报告及文献复习]

[Malignant cerebellar ganglioglioma. A case report and review of the literature].

作者信息

Mekni A, Chelly I, Haouet S, Zitouna M, Kchir N

机构信息

Service d'Anatomie et de Cytologie Pathologique, Hôpital La Rabta, 1007, Bab Saadoun, Tunis, Tunisie.

出版信息

Neurochirurgie. 2006 Jun;52(2-3 Pt 1):119-22. doi: 10.1016/s0028-3770(06)71206-1.

Abstract

Ganglioglioma is usually a well differentiated slowly growing mixed neuronal and glial neoplasm corresponding to WHO grade I or II. However, some gangliogliomas are considered to be WHO grade III because they exhibit anaplastic features in their glial component. Finally there are exceptionally rare cases of newly diagnosed gangliogliomas with grade IV changes in the glial component. We report a case of a 25-year-old woman with a family history of neurofibromatosis who presented initially with a World Health Organization grade IV anaplastic ganglioglioma (a mixed ganglion cell multiform tumor glioblastoma). Despite aggressive management, the patient died of disease in a relatively short period. Histologically, two cell populations were noted: a predominant glial component consisting in a multiform glioblastoma and ganglion cells supporting a diagnosis of ganglioglioma. Immunohistochemical analysis clearly distinguished the two tumor cell populations. Although other cases of grade III gangliogliomas and twelve cases of grade IV gangliogliomas have been reported, the present case is exceptional in that, to our knowledge, it is the second case of a patient who presented initially with a composite grade IV ganglioglioma and who was clinically followed up to the time of death. This case allows direct comparison between the histological findings in a multiform glioblastoma and a ganglioglioma. It also documents the aggressive biologic behavior of this complex neoplasm.

摘要

节细胞胶质瘤通常是一种分化良好、生长缓慢的混合性神经元和胶质肿瘤,相当于世界卫生组织(WHO)I级或II级。然而,一些节细胞胶质瘤被认为是WHO III级,因为它们在胶质成分中表现出间变特征。最后,还有极少数新诊断的节细胞胶质瘤,其胶质成分有IV级改变的情况。我们报告一例25岁女性患者,有神经纤维瘤病家族史,最初表现为世界卫生组织IV级间变性节细胞胶质瘤(一种混合性神经节细胞多形性肿瘤胶质母细胞瘤)。尽管采取了积极的治疗措施,患者仍在相对较短的时间内死于该疾病。组织学上,观察到两种细胞群:主要的胶质成分由多形性胶质母细胞瘤组成,以及支持节细胞胶质瘤诊断的神经节细胞。免疫组织化学分析清楚地区分了这两种肿瘤细胞群。虽然已经报道了其他III级节细胞胶质瘤病例和12例IV级节细胞胶质瘤病例,但本病例很特殊,据我们所知,这是第二例最初表现为复合性IV级节细胞胶质瘤且临床随访至死亡的患者。该病例使得多形性胶质母细胞瘤和节细胞胶质瘤的组织学发现能够直接比较。它还记录了这种复杂肿瘤的侵袭性生物学行为。

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