A5060706922- Sarcoma Diagnosis and Treatment
- Neuroblastoma Research and Treatments
- Soft tissue tumor case studies
- Neurofibromatosis and Schwannoma Cases
- Childhood Cancer Survivors' Quality of Life
- Testicular diseases and treatments
- Vascular Malformations and Hemangiomas
- Adrenal and Paraganglionic Tumors
- Prenatal Screening and Diagnostics
- Synthesis and Characterization of Heterocyclic Compounds
- Neuroendocrine Tumor Research Advances
- Antifungal resistance and susceptibility
- Cardiac tumors and thrombi
- Ear and Head Tumors
- Autoimmune and Inflammatory Disorders Research
- Full-Duplex Wireless Communications
- Bone Metabolism and Diseases
- Tumors and Oncological Cases
- Fungal Infections and Studies
- Glioma Diagnosis and Treatment
- Ocular Infections and Treatments
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Medical Imaging and Pathology Studies
- IgG4-Related and Inflammatory Diseases
- Bone health and treatments
Centre Hospitalier Universitaire Sainte-Justine
2022-2024
Centre Hospitalier Universitaire Amiens-Picardie
2015-2024
Université de Montréal
2022-2024
Abstract Purpose Our objectives were to compare overall survival (OS) and pulmonary relapse between patients with metastatic Ewing sarcoma (EWS) at diagnosis who achieve rapid complete response (RCR) those residual nodules after induction chemotherapy (non‐RCR). Patients methods This retrospective cohort study included children under 20 years EWS treated from 2007 2020 19 institutions in the Pediatric Surgical Oncology Research Collaborative. Chi‐square tests conducted for differences among...
Neuroblastoma management in children is multimodal and depends on multiple factors, including the possibility of complete surgical resection. Image-defined risk factors (IDRFs) are used to assess feasibility primary surgery. We studied changes IDRFs after neoadjuvant chemotherapy for thoracic neurogenic tumors.We performed a multicenter review 27 patients presenting with unresectable tumors. Patients received chemotherapy, according their group. IDRF at diagnosis before surgery were...
Abstract BACKGROUND The “central nervous system primitive neuroectodermal tumor” (CNS-PNET) nosology was removed from the World Health Organization (WHO) classification after DNA methylation profiling and new tumor entities characterized by specific recurrent genetic alterations were described. aim of this study to re-evaluate diagnosis CNS-PNET describe their clinical characteristics. METHODS Patients aged < 18 years with or unclassified tumor, who treated at Gustave Roussy between...
Voriconazole and vincristine are major therapeutics in paediatric haematology. However, the risk-benefit ratio of treatment invasive aspergillosis with voriconazole patients receiving vincristine-based chemotherapy remains unclear.We report severe peripheral central neurological disorders a 14-year-old girl T-cell acute lymphoblastic leukaemia pulmonary aspergillosis. The case describes strong exacerbation by vincristine-induced neuropathic pains. It shows high variability trough serum...
Abstract Background The objective of this study is to assess the concordance and added value combined comparative genomic hybridization plus single‐nucleotide polymorphism microarray (CGH/SNP) analyses in pediatric acute lymphoblastic leukemia (ALL) risk stratification compared conventional cytogenetic methods. Procedure This a retrospective that included patients aged 1–18 years diagnosed with de novo ALL at Sainte‐Justine Hospital between 2016 2021. Results from molecular were collected...
The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. also features annotations, reviews, short reports, images haematology Letters to the Editor.