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ISSN: 1896-6764
Neuropsychiatria i Neuropsychologia/Neuropsychiatry and Neuropsychology
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vol. 11
Case report

Recurrent atypical giant meningioma in the third ventricle of a child

Song-Ping Zheng
Chao You
Yan Ju

Neuropsychiatria i Neuropsychologia 2016; 11, 1: 35–38
Online publish date: 2016/06/16
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Meningioma originates from arachnoid cap cells and represents approximately 3% of primary intracranial tumors in children (Bhatoe et al. 2006). Most meningiomas are benign and occur by the side of the cerebral falx, on the cerebral convex, and on the sphenoidal ridge. Intraventricular meningiomas, especially of the third ventricle, are rare. This article reports and discusses a case of recurrence of a giant atypical meningioma in the third ventricle of a child.

Case report

A 12-year-old boy sought medical treatment in our hospital after suffering from headache for one and a half months, aggravated and accompanied by vomiting, and one week of gait dysfunction. A nervous system test found ataxia in the patient, and no other positive signs were present. Laboratory examinations found no significant abnormal conditions. Cerebral enhanced MRI showed a giant spherical space-occupying lesion in the third ventricle measuring 4.5 cm × 4 cm × 3 cm. The lesion entered the lateral ventricle upward and the anterior brain stem downward. The tumor showed low and high signals at T1 and T2, respectively, and was significantly homo­geneously enhanced after injection of gadolinium. Tumor excision was performed via a right frontal transcortical-transventricular approach. During surgery, the tumor was observably grey in color, tenacious, and had a sufficient blood supply. Borders with peripheral cerebral tissues were unclear. Total removal of the tumor under a microscope was successfully completed. The type of tumor could not be determined from an intraoperative frozen section. The postoperative pathological report showed that the tumor was atypical meningioma (WHO II), and r-knife treatment was supplemented. The condition of the patient significantly improved, and he was discharged. Nineteen months after surgery, the patient was readmitted to our hospital for headache and vomiting. Cerebral enhanced MRI indicated a homogeneous enhanced nodule in the third ventricle measuring approximately 2 cm × 2 cm × 2 cm, causing mild hydrocephalus (Fig. 1). Tumor excision via the same incision approach was performed once more. The recurrent tumor wrapped around the right middle cerebral artery; hence, subtotal removal was performed. The condition of the patient improved after surgery, and he was transferred to the Department of Oncology for whole-brain radiotherapy.


Meningioma of the third ventricle usually obstructs the circulation of cerebrospinal fluid, resulting in hydrocephalus, which increases intracranial pressure. Vision loss, endocrine diseases, and ataxia could also occur as the tumor oppresses peripheral structures (Buetow et al. 1991; Hug et al. 2000). Similar to most benign meningiomas, the reported atypical meningioma in the third ventricle presented a homogeneously enhanced nidus in cerebral CT and MRI and caused varying degrees of hydrocephalus in the child. Although such cases are rare, the possibility of meningioma should be considered preoperatively.
Given that the lateral ventricle was enlarged significantly and the tumor broke into the la­teral ventricle, excision of the tumor in the third ventricle via a right frontal transcortical-transventricular approach was performed under a microscope. The peripheral structure of the third ventricle is important. The blood supply of the tumor mainly originates from the medial posterior choroidal vessels. The essence of surgical removal is to protect normal nervous tissues around the lesion, to perform intratumoral excision carefully while avoiding traction, and to conduct border separation.
Pathologically, with reference to earlier studies of the WHO, the likelihood of recurrence of meningiomas with brain invasion is significantly high. During the latest re-grading of meningiomas by the WHO, “invasion into cerebral tissues” was added as one of the diagnostic criteria for atypical meningiomas (Huang et al. 1993). In the pathological section of the present case, tumor invasion into the cerebral parenchyma was seen (Fig. 2). With hematoxylin and eosin and phosphohistone-H3 staining, abnormal karyomitosis was observed to occur in less than 4 per 10 high-power fields. Immunohistochemical analysis indicated the following results: tumor cells GFAP(–), S100(–), Syn (–), EMA(–), 5% positive rate of Ki67. Tumor invasion into the cerebral parenchyma was observed in focal areas. Therefore, the case was diagnosed as an atypical meningioma (WHO level II).
In the existing English literature, only two cases of atypical meningioma in the third ventricle of children have been reported (Buetow et al. 1991; Komotor et al. 2012). This article reports the first case of recurrent atypical meningioma in the third ventricle of a child. With simple surgery, the recurrence rate of atypical meningiomas in five years is nearly 40% (Louis et al. 2007). The longest follow-up duration for children with atypical meningiomas in the third ventricle has been reported to be only one year. The long-term effects are unknown.
The scope of tumor excision is the main factor determining the recurrence of atypical meningiomas (Song et al. 2008). However, for third ventricle meningiomas with unclear borders, over-excision could injure the nervous system and blood vessels around the third ventricle, causing serious postoperative complications or neural functional damage. Therefore, excision of the lesion to the greatest extent without damage to important structures around the third ventricle is a great challenge for neurosurgeons. Radiotherapy, as a supplementary postoperative therapy to atypical meningioma excision, reduces the recurrence rate of the tumor (Louis et al. 2007).
Regardless of the type of therapy, atypical meningiomas frequently recur; in particular, atypical meningiomas with precise evidence of invasion into cerebral tissues have high recurrence rates recurrence rates (Table 1). Long-term, close follow-up examinations must be performed to be able to treat recurrent lesions as soon as possible.


This article reports the first case of recurrent atypical meningioma in the third ventricle of a child. Tumor invasion into cerebral tissues signified a higher recurrence rate. Excision of the tumor under a microscope without injury to normal cerebral tissues is an essential requirement for neurosurgeons. For such patients, long-term, close follow-up examinations must be conducted to monitor tumor recurrence.


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