[Anatomical variants of papillary craniopharyngiomas: analysis of surgical series].

Q4 Medicine
V V Ivanov, A N Konovalov, L V Shishkina, D V Fomichev, A N Shkarubo, M A Kutin, P L Kalinin
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引用次数: 0

Abstract

Background: Craniopharyngiomas are benign tumors of the chiasmal-sellar region of adults and children, prone to local invasion and recurrence. There are two morphological types of craniopharyngiomas - adamantinomatous (in children and adults) and papillary (PCPs) (mainly in adults). PCPs are a rarer type (15-20%). In the literature of recent years devoted to PCPs, two main variants of these tumors are distinguished: 1) solid intraventricular (III ventricle) and 2) monocystic with a small tumor component located outside III ventricle.

Objective: To investigate the pathogenesis of PCPs and clarify the causes of formation of different anatomical tumor variants.

Material and methods: The study included 34 adult patients with PCPs, among them 21 - women and 13 - men, who had undergone primary surgical treatment in the NMRC for Neurosurgery named after Academician N.N. Burdenko from 2017 to 2024. The inclusion criterion was the presence of suprasellar, extra-intraventricular and strictly ventricular localization according to the brain MRI data. Tumor resection was performed using microsurgical (12) and endoscopic transsphenoidal access (22). In all cases, intraoperative sampling of histological material was carried out, including both a solid part of the tumor and a tumor cyst capsule. «Papillary craniopharyngioma» diagnosis in all cases was histologically confirmed.

Results: Two main forms of PCP have been identified - solid intraventricular PCP (III ventricle) (24%) and PCP with pronounced monocystic component (76%). Cystic PCPs of two variants - suprasellar extraventricular (cisternal) cystic PCPs and cystic PCPs, displacing the III ventricle's floor and spreading into its cavity.

Conclusion: The existence of two main forms of PCPs - solid intraventricular and predominantly cystic is determined by the initial tumor growth site relative to the pia mater. The cause for formation of cystic forms of PCPs is their location under the pia mater, which participates in the cystic wall formation.

[乳头状颅咽管瘤的解剖变异:外科系列分析]。
背景:颅咽管瘤是发生于成人和儿童鞍交区的良性肿瘤,易局部侵袭和复发。颅咽管瘤有两种形态类型——金刚瘤(儿童和成人)和乳头状(pcp)(主要是成人)。pcp是罕见的类型(15-20%)。在近年来关于pcp的文献中,区分了两种主要的肿瘤变体:1)实心脑室内(III脑室)和2)单囊性,位于III脑室外的小肿瘤成分。目的:探讨pcp的发病机制,明确不同解剖结构肿瘤变异的形成原因。材料和方法:该研究纳入了34例成年pcp患者,其中21例女性,13例男性,他们于2017年至2024年在以N.N. Burdenko院士命名的NMRC神经外科接受了初级手术治疗。纳入标准是根据脑MRI资料存在鞍上、脑室外和严格的脑室定位。肿瘤切除采用显微外科手术(12)和内镜下经蝶窦通路(22)。在所有病例中,术中都进行了组织材料取样,包括肿瘤的实体部分和肿瘤囊肿囊。所有病例的“乳头状颅咽管瘤”诊断均经组织学证实。结果:已确定两种主要形式的PCP -实心脑室内PCP (III脑室)(24%)和明显的单囊性PCP(76%)。囊性pcp有两种变体——鞍上室外(池)囊性pcp和囊性pcp,移位第三脑室底并向腔内扩散。结论:pcp的存在主要有两种形式——实心脑室内和以囊性为主,这是由肿瘤相对于硬膜的初始生长部位决定的。pcp囊性形成的原因是其位于脑膜下,参与囊壁形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
75
期刊介绍: Scientific and practical peer-reviewed journal. This publication covers the theoretical, practical and organizational problems of modern neurosurgery, the latest advances in the treatment of various diseases of the central and peripheral nervous system. Founded in 1937. English version of the journal translates from Russian version since #1/2013.
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