Tumor surveillance for children and adolescents with cancer predisposition syndromes: The psychosocial impact reported by adolescents and caregivers

K van Engelen, M Barrera… - Pediatric Blood & …, 2021 - Wiley Online Library
Purpose Individuals with cancer predisposition syndromes (CPS) are often followed in
cancer screening programs, which aim to detect early stage tumors. While cancer …

Nephron sparing surgery for unilateral Wilms tumor in children with predisposing syndromes: single center experience over 10 years

RLP Romão, JL Pippi Salle, C Shuman… - The Journal of …, 2012 - auajournals.org
Purpose: Unilateral Wilms tumors associated with predisposing syndromes are treated with
preoperative chemotherapy followed by surgical resection. We describe our experience with …

Management of familial cancer: sequencing, surveillance and society

N Samuel, A Villani, CV Fernandez… - Nature Reviews Clinical …, 2014 - nature.com
The clinical management of familial cancer begins with recognition of patterns of cancer
occurrence suggestive of genetic susceptibility in a proband or pedigree, to enable …

Mesenchymal hamartoma or embryonal sarcoma of the liver in childhood: a difficult diagnosis before complete surgical excision

BE Wildhaber, E Montaruli, F Guérin… - Journal of pediatric …, 2014 - Elsevier
Background Clinical experience shows that the primary diagnosis of mesenchymal
hamartoma (MHL) and embryonal sarcoma of the liver (ESL) recurrently is mistaken, leading …

[HTML][HTML] Genetic syndromes associated with overgrowth in childhood

JM Ko - Annals of pediatric endocrinology & metabolism, 2013 - ncbi.nlm.nih.gov
Overgrowth syndromes comprise a diverse group of conditions with unique clinical,
behavioral and molecular genetic features. While considerable overlap in presentation …

The technologically integrated oncosimulator: combining multiscale cancer modeling with information technology in the in silico oncology context

G Stamatakos, D Dionysiou, A Lunzer… - IEEE Journal of …, 2013 - ieeexplore.ieee.org
This paper outlines the major components and function of the technologically integrated
oncosimulator developed primarily within the Advancing Clinico Genomic Trials on Cancer …

Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith–Wiedemann syndrome

A Mussa, GB Ferrero, B Ceoloni, E Basso… - European journal of …, 2011 - Springer
Beckwith–Wiedemann syndrome is an overgrowth disorder characterized by neonatal
macrosomia, abdominal wall defects, macroglossia, renal anomalies, organomegaly …

Imaging for Staging of Pediatric Abdominal Tumors: An Update, From the AJR Special Series on Cancer Staging

CE Morin, M Artunduaga, GR Schooler… - American Journal of …, 2021 - Am Roentgen Ray Soc
The three most common pediatric solid tumors of the abdomen are neuroblastoma, Wilms
tumor, and hepatoblastoma. These embryonal tumors most commonly present in the first …

Genetic testing and tumor surveillance for children with cancer predisposition syndromes

A Rao, J Rothman, KE Nichols - Current opinion in pediatrics, 2008 - journals.lww.com
Advances in the understanding of cancer predisposition and implementation of standardized
cancer surveillance protocols have improved the outcome for certain patients. Future …

Incidence of abdominal tumors in syndromic and idiopathic hemihypertrophy/isolated hemihyperplasia

M Dempsey-Robertson, D Wilkes, A Stall… - Journal of Pediatric …, 2012 - journals.lww.com
Background: There is a reported increased risk of intra-abdominal tumors in children with
both syndromic (SH) and isolated idiopathic hemihyperplasia (IH). Recommendations for …