2007
DOI: 10.3174/ajnr.a0601
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Rhabdoid Meningioma: Clinical Features and MR Imaging Findings in 15 Patients

Abstract: BACKGROUND AND PURPOSE:Rhabdoid meningioma (RM) is a recently described variant of malignant meningioma, with radiologic features currently not well characterized in the medical literature. The purpose of this study was to describe and characterize clinical features and imaging findings associated with RM.

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Cited by 41 publications
(28 citation statements)
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“…The diagnosis of RM was strictly based on previously published criteria [1][2][3]. At diagnosis, the 59-year-old male patient had a mass in the floor of the right middle cranial fossa.…”
Section: Patient and Samplementioning
confidence: 99%
See 1 more Smart Citation
“…The diagnosis of RM was strictly based on previously published criteria [1][2][3]. At diagnosis, the 59-year-old male patient had a mass in the floor of the right middle cranial fossa.…”
Section: Patient and Samplementioning
confidence: 99%
“…Despite radical surgical excision and adjuvant radio-and chemotherapy, RM usually exhibits early recurrence, metastasis, and poor prognosis. Previous reports have mainly focused on clinical and histological features of RM, but rarely on its oncogenesis, particularly the tumor-initiating cells (TICs) [1][2][3].…”
Section: Introductionmentioning
confidence: 99%
“…To the best of our knowledge, 50 cases of RM, including three case series, have been published in the English-language literature. 2,3,[8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23] Rhabdoid features usually emerge as a focal change, in either benign or malignant meningiomas of other histological subtypes. 2,3 Pure variants of such tumors are very uncommon, but rhabdoid components tend to be more prominent in recurrent tumors.…”
Section: Discussionmentioning
confidence: 99%
“…Generally, the prognosis is poor, and many case reports are available on pediatric patients in the literature. On CT and MRI, the tumor demonstrates severe peritumoral edema in 75 %, cyst formation in 38 %, and mixed bone destruction and hyperostosis in 33 % of the cases [27].…”
Section: Other Histological Variantsmentioning
confidence: 99%