[Congenital basal encephaloceles involving functionally important structures].

Q4 Medicine
N A Chernikova, L A Satanin, E V Shelesko, G V Danilov, S B Agrba, A N Shkarubo, N A Mazerkina, M L Satanina
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引用次数: 0

Abstract

In rare cases, basal encephaloceles can include important brain structures (pituitary gland, chiasm, third ventricle walls, cerebral vessels).

Material and methods: We reviewed 43 articles (78 cases) devoted to basal encephaloceles involving functionally important structures. Analysis included transsphenoidal and sphenoethmoidal hernias.

Results: Nasal breathing disorders were found in 76.9% of cases, decreased visual acuity - 53.8%, endocrine disorders - 44.9%, nasal CSF leakage - 14.1%, meningitis - 10.3%. Concomitant malformations occurred in 85.9%. Severe respiratory disorders (52.6%, p<0.05) and multiple concomitant malformations (71.7%, p<0.05) were more common among patients with sphenoethmoidal encephalocele. Among 78 patients, 73.1% underwent surgery while follow-up was preferable in 26.9% of cases. There was progression of endocrine disorders (9.5%), visual impairment (4.8%) and nasal breathing disorders (4.8%) in follow-up period. Surgical treatment also has many risks. Transcranial, transnasal, transoral and combined approaches are currently used. It was not possible to establish the most effective surgical approach due to heterogeneous clinical data. Postoperative complications occurred in 47.4% of cases (endocrine disorders - 33.3%, CSF leakage - 8.8%, visual impairment - 1.8%, infectious complications - 14%). Mortality rate was 3.5%.

Conclusion: Congenital basal encephalocele involving functionally important structures is an extremely rare developmental defect. Such patients often have concomitant anomalies. Comprehensive examination is necessary to estimate the structures included in hernial sac and concomitant diseases. Treatment strategy should be determined individually after thorough examination and comparison of all risks. Surgical treatment is associated with high risk of complications due to damage to the structures comprising encephalocele.

[涉及重要功能结构的先天性基底脑畸形]。
在极少数病例中,基底脑畸形可包括重要的脑结构(垂体、脊管、第三脑室壁、脑血管):我们查阅了 43 篇文章(78 个病例),专门讨论了涉及重要功能结构的基底脑畸形。分析包括经蝶疝和蝶窦疝:结果:76.9%的病例出现鼻呼吸障碍,53.8%的病例视力下降,44.9%的病例出现内分泌紊乱,14.1%的病例出现鼻腔CSF渗漏,10.3%的病例出现脑膜炎。85.9%的病例伴有畸形。严重的呼吸系统疾病(52.6%,ppConclusion:先天性基底脑畸形涉及重要的功能结构,是一种极为罕见的发育缺陷。这类患者通常伴有异常。有必要进行全面检查,以估计疝囊内的结构和并发疾病。治疗策略应在全面检查和比较所有风险后逐一确定。手术治疗会对疝囊结构造成损伤,因此并发症的风险很高。
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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