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首页> 外文期刊>Pediatric blood & cancer >Posterior fossa syndrome after posterior fossa surgery in children with brain tumors.
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Posterior fossa syndrome after posterior fossa surgery in children with brain tumors.

机译:儿童脑肿瘤后颅窝手术后颅窝综合征。

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BACKGROUND: Posterior fossa syndrome (PFS) is defined as the temporary and complete loss of speech after posterior fossa surgery. The goal of this study was to identify incidence and risk factors for PFS and to determine accompanying neurobehavioral and psychologic problems. PROCEDURE: Between May 2007 and April 2009, children with brain tumors having posterior fossa surgery were evaluated neurologically and psychologically in preoperative and postoperative period. RESULTS: PFS developed in 9 patients among 36 (25%) included in the study. Mutism continued for 120 days in one patient. Histopathological diagnosis (P = 0.05), location of the tumor (P = 0.05) and socioeconomic level of the family (P = 0.06) gave the significant results in relation with the PFS by univariate analyses. In multivariate analysis the risk of developing PFS was found 7.2 times higher in patients with medulloblastoma, 6.7 times higher in tumors located at the midline, 5.7 times higher in families with low socioecnomic level. Intelligence quotients of the patients in PFS and other group (P = 0.85) with Wechsler Intelligence Scale for Children and the results of the Denver II Developmental Screening Test were not significant statistically (P = 0.5). CONCLUSION: The diagnosis of medulloblastoma, midline location of the tumor and low socioeconomic level of the families are important risk factors for the development of PFS. These findings support the hypothesis that temporary ischemia and edema due to retracted and manipulated dentate nuclei and superior cerebellar pedincles may be the cause of mutism.
机译:背景:后颅窝综合征(PFS)的定义是后颅窝手术后暂时性和完全性的语言丧失。这项研究的目的是确定PFS的发生率和危险因素,并确定伴随的神经行为和心理问题。程序:自2007年5月至2009年4月,对接受颅后窝手术的脑瘤患儿在术前和术后进行神经和心理方面的评估。结果:研究中36名(25%)的9名患者发生了PFS。一名患者的默症持续了120天。通过单因素分析,与PFS相关的组织病理学诊断(P = 0.05),肿瘤位置(P = 0.05)和家庭的社会经济水平(P = 0.06)得到了显着结果。在多变量分析中,髓母细胞瘤患者发生PFS的风险高7.2倍,中线肿瘤高6.7倍,社会经济水平低的家庭高5.7倍。 PFS和其他组患者的智商(P = 0.85)和儿童的韦氏智力量表以及Denver II发育筛查测试的结果在统计学上均无统计学意义(P = 0.5)。结论:髓母细胞瘤的诊断,肿瘤的中线位置和家庭的社会经济水平低是PFS发展的重要危险因素。这些发现支持这样的假说,即由于齿状核的缩回和操纵以及小脑上半轴的暂时性缺血和水肿可能是变的原因。

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