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http://dx.doi.org/10.1007/s00381-015-2943-8 | DOI Listing |
Pediatr Hematol Oncol
February 2024
Department of Pediatric Onco-Hematology, Hôpital d'Enfants de La Timone, AP-HM, Marseille, France.
Solid tumors or predisposition syndromes are increasingly suspected before birth. However optimal management and outcomes remain unclear. We have performed a ten-year retrospective study of oncologic indications of prenatal diagnosis in public hospitals in Marseille.
View Article and Find Full Text PDFFetal Pediatr Pathol
August 2022
Pathology, Institute of Postgraduate Medical Education and Research, Kolkata, India.
Neuroblastoma can arise from extra-adrenal sites in the paraspinal sympathetic chain, including the presacral region, where they must be differentiated from an immature or malignant neural lesion arising from a teratoma.We describe two congenital presacral neuroblastomas. The main clinical differential diagnoses were sacrococcygeal teratoma and meningomyelocele.
View Article and Find Full Text PDFPrenat Diagn
January 2020
Surgery Department Center for Fetal Diagnosis and Treatment, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Fetal tumors and other dysplastic masses are relatively rare. They are usually the result of failure of differentiation and maturation during embryonic or fetal life; dysplastic lesions may be the consequence of an obstruction sequence. In this review, we present the most commonly encountered tumors and masses seen during fetal life.
View Article and Find Full Text PDFClin Nucl Med
May 2019
Department of Nuclear Medicine, JIPMER, Puducherry, Pondicherry, India.
A 5-month-old boy with ultrasonography showing bilateral hydronephrosis, referred for renal scan. On Tc-L,L,ethylenedicysteine (Tc-LLEC) renal scan, tracer blush in flow images in the region of urinary bladder was seen and tumor mass was suspected. Contrast-enhanced CT showed a soft tissue mass in sacrococcygeal region.
View Article and Find Full Text PDFAim: Neonatal tumours represents less than 2% of all childhood cancers. The biological behaviour of this tumours will differ in older children. The tumours's biological differences and the immature physiological characteristics of newborns represent a great therapeutically challenge making newborns vulnerable.
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