El-Ayadi, M., K. Egervari, D. Merkler, T. A. McKee, F. Gumy-Pause, D. Stichel, D. Capper, T. Pietsch, M. Ansari, and A. O. von Bueren, "Concurrent IDH1 and SMARCB1 Mutations in Pediatric Medulloblastoma: A Case Report.", Frontiers in neurology, vol. 9, pp. 398, 2018. Abstract

Isocitrate Dehydrogenase-1 ( is a driver gene in several cancers including brain tumors such as low-grade and high-grade gliomas. Mutations of were described in atypical teratoid rhabdoid tumors and to date have not been associated with the pathogenesis of medulloblastoma. We report concurrent and mutations in a medulloblastoma patient. We searched the catalog of somatic mutations in cancer (COSMIC) database and other mutation databases and -to our knowledge- this is the first reported case of medulloblastoma harboring both mutations together. Our patient is a 13-year-old male presenting with headache and vomiting at diagnosis. MRI revealed left cerebellar expansive lesion with no evidence of metastasis. A histopathological diagnosis of desmoplastic/nodular medulloblastoma was made after complete resection of the tumor. Immunophenotypic characterization and methylation profiling suggested a medulloblastoma with SHH activation. Next generation sequencing of a panel of 400 genes revealed heterozygous somatic (p.R132C), (p.R201Q), and (p.L625T) mutations. The patient was treated according to the HIT-SIOP PNET 4 protocol. He is in complete remission more than 2 years after diagnosis. In conclusion, increasing use of high throughput sequencing will certainly increase the frequency with which rare mutations or mutation combinations are identified. The exact frequency of this mutation combination and whether it has any particular therapeutic implications or prognostic relevance requires further investigation.

El-Ayadi, M., M. Ansari, C. D. Kühnöl, A. Bendel, D. Sturm, T. Pietsch, C. M. Kramm, and A. O. von Bueren, "Occurrence of high-grade glioma in Noonan syndrome: Report of two cases.", Pediatric blood & cancer, vol. 66, issue 5, pp. e27625, 2019. Abstract

Noonan syndrome (NS) is an autosomal dominant disorder commonly caused by PTPN11 germline mutations. Patients are characterized by short stature, congenital heart defects, facial dysmorphism, and increased risk of malignancies including brain tumors. Commonly associated brain tumors are dysembryoplastic neuroepithelial tumor and low-grade glioma. We report two cases of anaplastic astrocytoma with PTPN11-related NS. We conducted a systematic search of medical databases looking for other reported cases of high-grade glioma associated with NS and identified 24 cases of brain tumors, all of which were low-grade glial or glioneuronal tumors except for one case of medulloblastoma.

Perez, A., L. Merlini, M. El-Ayadi, C. Korff, M. Ansari, and A. O. von Bueren, "Comment on: Ketogenic diet treatment in recurrent diffuse intrinsic pontine glioma in children: A safety and feasibility study.", Pediatric blood & cancer, vol. 66, issue 7, pp. e27664, 2019.
El-Ayadi, M. M., M. Ansari, C. Kuhnol, A. Bendel, D. Sturm, T. Pietsch, C. Kramm, and A. VonBuren, "Noonan syndrome can be associated with high grade glioma; a report of two cases", 22nd Annual Meeting for Society of Neuro-oncology, San Francisco, California, USA, 17 November, 2017.
El-Ayadi, M., M. Ansari, D. Sturm, G. Gerrit, M. Warmuth-Metz, C. Kramm, and A. VonBuren, "High-grade glioma in very young children: a rare and particular patient population ", oncotarget, vol. 8, issue 8, pp. 64564-64578, 2017.
Shalaby, L., A. Elhaddad, Sonia Magdy, and M. El-Ayadi, "Relapse Risk Group Parameters of Newly Diagnosed Pediatric Acute Myeloid Leukemia Patients Treated at Children Cancer Hospital in Egypt", Pediatric Blood & Cancer, vol. 57, issue 5, pp. 773 - 773, 2011.
El-Ayadi, M., S. Aboul-Naga, L. Shalaby, and S. Salem, Disease Outcome of Newly Diagnosed Pediatric Acute Myeloid Leukemia Patients treated at Children Cancer Hospital, Egypt, , Cairo, Cairo, 2010.
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