2010
DOI: 10.3121/cmr.2010.877
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Large Supratentorial Cortical Ependymoma in a Child

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Cited by 19 publications
(19 citation statements)
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“…In the present series, the majority of the tumors were irregularly-lobulated, which was likely due to the fact that the tumors grew actively or the cell proliferation was not uniform. The tumors were hypointense to isointense relative to the gray matter on non-enhanced T1WI, and they were hyperintense or slightly hypointense on T2WI, similar to the appearances of other intracranial tumors (24). The architecture of the tumors in the present study was commonly heterogeneous, correlating with the MRI results and the microscopic findings; heterogeneous intensity can indicate various components of the lesion, such as cysts, necrosis, intratumoral hemorrhage, calcification, fibrosis or vascular proliferation (25).…”
supporting
confidence: 70%
“…In the present series, the majority of the tumors were irregularly-lobulated, which was likely due to the fact that the tumors grew actively or the cell proliferation was not uniform. The tumors were hypointense to isointense relative to the gray matter on non-enhanced T1WI, and they were hyperintense or slightly hypointense on T2WI, similar to the appearances of other intracranial tumors (24). The architecture of the tumors in the present study was commonly heterogeneous, correlating with the MRI results and the microscopic findings; heterogeneous intensity can indicate various components of the lesion, such as cysts, necrosis, intratumoral hemorrhage, calcification, fibrosis or vascular proliferation (25).…”
supporting
confidence: 70%
“…GTR (10 of 14 patients in our series) is the optimal therapy for symptomatic supratentorial parenchymal ependymomas (2,3,(5)(6)(7)(8)(9)12,15,(18)(19)(20)(21)23). In the present series, the postoperative care of patients depended on the operative procedure.…”
Section: Treatment Proceduresmentioning
confidence: 86%
“…We did not recommend adjuvant therapy such as radiotherapy or chemotherapy if gross total surgical removal (GTR) had been achieved in the patients with low grade tumors (The WHO Grade I and Grade II ependymomas). The radiotherapy should only be given to patients with anaplastic ependymomas and tumors in locations where total excision is not possible (9,16,19,21).…”
Section: Surgical Proceduresmentioning
confidence: 99%
“…The clinical and pathological characteristics of supratentorial ependymomas in children are not well identified in the literature, because most series deal with ependymomas regardless of their location or age of the patient. Extraventricular ependymomas are especially rare, and while they have definite ependymal morphology, their histogenesis remains uncertain 10) . However, in some articles the pathogenesis of supratentorial, extraventricular, cortical, and ectopic ependymoma were explained in other ways.…”
Section: Discussionmentioning
confidence: 99%
“…The researchers concluded that post-operative radiotherapy did not play a role in treatment. However, in another recent study of supratentorial ependymomas, it has been suggested that radiotherapy should be given to patients with anaplastic ependymomas and in cases where only partial resection of either benign or malignant tumors has been achieved 10) . As mentioned previously, ependymomas can infiltrate surrounding normal tissue, so incomplete removal of the tumor during surgery may lead to a bad prognosis.…”
Section: Treatment and Prognosismentioning
confidence: 99%