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Background: Image-defined risk factors (IDRFs) were promulgated for predicting the feasibility and safety of complete primary tumor resection in children with neuroblastoma (NB). There is limited understanding of the impact of individual IDRFs on resectability of the primary tumor or patient outcomes. A multicenter database of patients with high-risk NB was interrogated to answer this question.
Design/methods: Patients with high-risk NB (age <20 years) were eligible if cross-sectional imaging was performed at least twice prior to resection. IDRFs and primary tumor measurements were recorded for each imaging study. Extent of resection was determined from operative reports.
Results: There were 211 of 229 patients with IDRFs at diagnosis, and 171 patients with IDRFs present pre-surgery. A ≥90% resection was significantly more likely in the absence of tumor invading or encasing the porta hepatis, hepatoduodenal ligament, superior mesenteric artery (SMA), renal pedicles, abdominal aorta/inferior vena cava (IVC), iliac vessels, and/or diaphragm at diagnosis or an overlapping subset of IDRFs (except diaphragm) at pre-surgery. There were no significant differences in event-free survival (EFS) and overall survival (OS) when patients were stratified by the presence versus absence of any IDRF either at diagnosis or pre-surgery.
Conclusion: Two distinct but overlapping subsets of IDRFs present either at diagnosis or after induction chemotherapy significantly influence the probability of a complete resection in children with high-risk NB. The presence of IDRFs was not associated with significant differences in OS or EFS in this cohort.
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http://dx.doi.org/10.1002/pbc.31218 | DOI Listing |
Quant Imaging Med Surg
August 2025
Nuclear Medicine Department, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Background: Congenital neuroblastoma represents an early-onset form of neuroblastoma. This study aims to evaluate the imaging features of I-metaiodobenzylguanidine (I-MIBG) single-photon emission computed tomography (SPECT)/computed tomography (CT) and their correlation with the clinical characteristics of localized congenital neuroblastoma.
Methods: We retrospectively collected imaging and clinical data from congenital neuroblastoma patients who underwent I-MIBG SPECT/CT.
European J Pediatr Surg Rep
January 2025
Pediatric Surgery Department, IRCCS, Istituto Giannina Gaslini, Genoa, Italy.
We report the use of endoscopic cholecystoduodenostomy in a 6-year-old child to manage postanastomotic stricture of the common bile duct (CBD) secondary to an intraoperative injury sustained during the resection of an abdominal neuroblastoma (NB). The patient was diagnosed with stage M NB, characterized by dissemination to the bone marrow and vertebrae, and MYCN amplification. Following multiple cycles of chemotherapy and subsequent hematopoietic stem cell transplantation, the patient was scheduled for surgical resection.
View Article and Find Full Text PDFJ Comput Assist Tomogr
July 2025
Department of Radiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Neurodevelopment and Cognitive Disorders.
Objective: Anatomic image-defined risk factors (IDRFs) and metabolic metrics from PET/CT imaging can evaluate tumor biology and guide clinical decision-making in neuroblastoma. This study explored the association between IDRFs and 18F-FDG PET/CT metabolic metrics in neuroblastoma and compared their prognostic value.
Methods: A retrospective analysis was conducted on 24 neuroblastoma patients who underwent pretreatment CECT and 18F-FDG PET/CT imaging.
J Bone Metab
May 2025
Department of Rheumatology, Hospital Universitari de Bellvitge, Barcelona, Spain.
Background: To investigate the contribution of radiological characteristics of baseline fragility vertebral fractures (FVF) and clinical characteristics to the development of radiological worsening (RW).
Methods: Patients were recruited between 2015 and 2018. The primary outcome was the identification of RW in a radiological second image, defined as the progression of prevalent FVF, new FVF, or both.
J Indian Assoc Pediatr Surg
March 2025
Department of Paediatric Surgery, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
Background: Adrenal tumors account for 0.2%-1% of all tumors in children. They can be benign or malignant, secretory or nonsecretory, and can arise either from the cortex or medulla.
View Article and Find Full Text PDF