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[原始生发起源的脑肿瘤]

[Cerebral tumors of primitive germinal origin].

作者信息

Juif J G, Maitrot D, Pierson M, Heldt N, Buchheit F, Luckel J C

出版信息

Arch Fr Pediatr. 1977 Apr;34(4):335-46.

PMID:196564
Abstract

The authors attempt to justify the term cerebral tumour of primitive germinal origin from four of their own cases and a review of the literature. They emphasise the specific features. The tumours are more common in boys and involve the pineal, the walls of the third ventricle, the hypothalamus and the posterior pituitary. Several histological types may be distinguished by the degree of differentiation but the stromal reaction, which is partly responsible for the symptoms, is always present. The clinical course of the illness is biphasic. The first is manifest by endocrine disorders and is of relatively long duration. Water homeostasis is always affected and may be associated with other hypothalamic disorders. In the second phase, neurological symptoms and raised intracranial pressure appear. Surgical removal is not always possible, but radiotherapy improves the outlook.

摘要

作者通过自身的4例病例并结合文献综述,试图论证“原始生发起源的脑肿瘤”这一术语。他们强调了其特定特征。这些肿瘤在男孩中更为常见,累及松果体、第三脑室壁、下丘脑和垂体后叶。根据分化程度可区分出几种组织学类型,但部分导致症状的间质反应始终存在。该疾病的临床病程呈双相性。第一阶段表现为内分泌紊乱,持续时间相对较长。水稳态总是受到影响,可能与其他下丘脑紊乱相关。在第二阶段,出现神经症状和颅内压升高。手术切除并非总是可行,但放疗可改善预后。

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