... Blood Cancer. 2012 ; 58 ( 6 ): 905 – 909 . 4. Zaytseva M , Valiakhmetova A , Yasko L , et al . Molecular heterogeneity of pediatric choroid plexus carcinomas determines the distinctions in clinical course and prognosis . Neuro Oncol . 2023 ; 25 ( 6 ): 1132 – 1145 . 5...

.... Ruland V , Hartung S , Kordes U , et al . Choroid plexus carcinomas are characterized by complex chromosomal alterations related to patient age and prognosis . Genes Chromosomes Cancer. 2014 ; 53 ( 5 ): 373 – 380 . 3. Thomas C , Soschinski P , Zwaig M , et al...

..., Standard Journals Publication Model ( https://dbpia.nl.go.kr/pages/standard-publication-reuse-rights ) Science for Children Key Points Choroid plexus carcinomas can be stratified into risk groups based on gene expression profiles; Choroid plexus carcinomas with “hyperactive” oncogenic pathways...

... ( Nov ): 2579 – 2605 . 27. Duffner   PK , Kun   LE , Burger   PC , et al   Postoperative chemotherapy and delayed radiation in infants and very young children with choroid plexus carcinomas . Pediatr Neurosurg.   1995 ; 22 ( 4 ): 189 – 196 . 28. Chow   E , Reardon...

... atypical choroid plexus papillomas (aCPPs, WHO grade II), and 31 choroid plexus carcinomas (CPCs, WHO grade III) by Illumina Infinium HumanMethylation450 Bead Chip Array. Results Unsupervised hierarchical clustering identified 3 subgroups: methylation cluster 1 (pediatric CPP and aCPP of mainly...

... and show INI1 protein loss. Histological and immunohistochemical features did not correspond to established tumor types, including atypical teratoid/rhabdoid tumors, medulloepithelioma, choroid plexus carcinoma, and ependymoma. Fluorescence in situ hybridization analyses failed to identify chromosomal...

...Astrid Jeibmann; Martin Hasselblatt; Joachim Gerss; Brigitte Wrede; Rupert Egensperger; Rudi Beschorner; Volkmar H. J. Hans; Christian H. Rickert; Johannes E. Wolff; Werner Paulus As shown in Table 1 , the 24 cases of choroid plexus carcinoma as well as the 140 cases of choroid plexus papilloma...

...Alexander R. Judkins; Peter C. Burger; Ronald L. Hamilton; Bette Kleinschmidt-DeMasters; Arie Perry; Scott L. Pomeroy; Marc K. Rosenblum; Anthony T. Yachnis; Holly Zhou; Lucy B. Rorke; Jaclyn A. Biegel Atypical teratoid/rhabdoid tumor (AT/RT) BAF47 Choroid plexus carcinoma hSNF5...

... mutation or whether it reflects the genetic background of the affected families. Astrocytoma Choroid plexus carcinoma Glioblastoma p53 germline mutation ...

... Abstract OBJECTIVE: Choroid plexus carcinomas are rare tumors with dismal prognosis. The role of surgery has been well established, but the benefit of either chemotherapy or radiotherapy remains controversial. To determine prognostic factors and effects of different therapeutic modalities on the outcome...

... plexus carcinomas in siblings aged II months and 10 years were examined by light microscopy and immunocytochemistry. One case was studied by electron microscopy. Choroid plexus carcinoma is rare, with approximately 24 reported cases in children. Predicting the behavior of choroid plexus tumors from...

... and a full/tense fontanelle. The chapter reviews the differential diagnoses for macrocephaly. Imaging, including magnetic resonance spectroscopy, revealed a highly vascular intraventricular mass with some areas of likely necrosis, suggesting choroid plexus carcinoma. The authors review the preoperative...

... papilloma, and choroid plexus carcinoma. Choroid plexus carcinomas can occur in the context of Li–Fraumeni syndrome, where the TP53 germline mutation predisposes patients to a wide range of neoplasms. Treatment of these tumours is challenging, due to their high vascularity and the young age...