Neuroblastoma of the Bone and Bone Marrow Without an Apparent Primary Site: Report of 4 Cases With Long-term Follow-up.
imaging studies
long-term follow-up
neural crest tumors
neuroblastoma
surg path
without an apparent primary site
Journal
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
ISSN: 1615-5742
Titre abrégé: Pediatr Dev Pathol
Pays: United States
ID NLM: 9809673
Informations de publication
Date de publication:
Historique:
pubmed:
3
1
2019
medline:
22
1
2020
entrez:
3
1
2019
Statut:
ppublish
Résumé
Children with neuroblastoma rarely present with metastatic disease without identifiable primary tumors. We describe the clinical and histopathologic characteristics of 4 patients aged 1, 7, 7, and 11 years with neuroblastoma involving bone or bone marrow without an apparent primary site. One patient presented with a periorbital bone lesion, 1 presented with a distal femoral lesion, and 2 presented with diffuse bone marrow involvement. All tumors were negative for
Identifiants
pubmed: 30600764
doi: 10.1177/1093526618822597
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM