Non‐rhabdomyosarcoma soft tissue sarcomas diagnosed in patients at a young age. An overview of clinical, pathological, and molecular findings

Objective Disease spectrum in pediatric sarcoma differs substantially from adults. We report a cohort of very young children with non‐rhabdomyosarcoma soft tissue sarcoma (NRSTS) detailing their molecular features, treatment, and outcome. Methods We report features of consecutive children (age

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Bibliographic Details
Published in:Pediatric blood & cancer 2021-08, Vol.68 (8), p.e29022-n/a
Main Authors: Renzi, Samuele, Cullinan, Noelle, Cohen‐Gogo, Sarah, Langenberg‐Ververgaert, Karin, Michaeli, Orli, Alkendi, Jalila, Kanwar, Nisha, Lo, Winnie, Villani, Anita, Shlien, Adam, Malkin, David, Ryan, Anne L., Gallinger, Bailey, Ingley, Katrina, Hopyan, Sevan, Gupta, Abha, Chami, Rose
Format: Article
Language:English
Subjects:
Age
Chemotherapy
Children
Disease-Free Survival
Female
Fibrosarcoma
Fibrosarcoma - diagnosis
Fibrosarcoma - therapy
Hematology
Humans
Infant
infant sarcoma
Infant, Newborn
Male
Malignant rhabdoid tumor
Metastases
molecular diagnostics
Oncology
Patients
Pediatrics
Rhabdoid Tumor - diagnosis
Rhabdoid Tumor - therapy
Rhabdomyosarcoma
Sarcoma
Sarcoma - diagnosis
Sarcoma - therapy
Soft Tissue Neoplasms - diagnosis
Soft Tissue Neoplasms - therapy
Soft tissue sarcoma
Surgery
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Description
Summary:Objective Disease spectrum in pediatric sarcoma differs substantially from adults. We report a cohort of very young children with non‐rhabdomyosarcoma soft tissue sarcoma (NRSTS) detailing their molecular features, treatment, and outcome. Methods We report features of consecutive children (age
ISSN:1545-5009
1545-5017
DOI:10.1002/pbc.29022