1.
An. pediatr. (2003. Ed. impr.)
; 95(4): 267-268, Oct. 2021. tab, ilus
Artigo
em Espanhol
| IBECS
| ID: ibc-207789
RESUMO
No disponible
Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Neoplasias do Córtex Suprarrenal/diagnóstico por imagem , Neoplasias do Córtex Suprarrenal/diagnóstico , Neoplasias do Córtex Suprarrenal/etiologia , Neoplasias do Córtex Suprarrenal/tratamento farmacológico , Hormônios
2.
An Pediatr (Engl Ed)
; 95(4): 267-268, 2021 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34479837
3.
4.
Pediatr Blood Cancer
; 67(11): e28679, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32860659
RESUMO
Composite sarcoma of bone is a very rare entity that primarily affects adolescent and young adult patients. It usually combines areas of liposarcoma and osteosarcoma, and up to 60% of cases have metastatic disease at diagnosis. It is a highly aggressive pathology with intrinsic resistance to bone sarcoma conventional treatments. The prognosis is poor, with long-term survival rates not exceeding 30%. We present the case of an adolescent female diagnosed with an aggressive composite sarcoma of bone with rhabdomyosarcoma foci and loco-regional lymph node involvement.
