Congenital embryonal rhabdomyosarcoma with prenatal onset
Iranian Journal of Pediatrics. 2008; 18 (1): 62-66
em Inglês
| IMEMR
| ID: emr-143517
ABSTRACT
Rhabdomyosarcoma [RMS] is the single most common type of soft tissue sarcoma in children and adolescents but it is extraordinarily rare in neonates. Extremity RMS comprises 20% of all sites, occurs more commonly in the leg than in the arm and accounts for 9% of all RMS cases. According to our review, this is the second case of RMS on day one of life with congenital, antenatal feature, and postnatal progressive clinical course of a large tumor of the hand [pretreatment staging T2bN1M0] with embryonic histological subtype and unfavorable prognosis. The patient is a term newborn boy with huge mass in the right hand and palpable lymph node in subaxillar region. Congenital embryonal rhabdomyosarcoma is a rare form of sarcomas with congenital in nature, antenatal feature and post natal progressive clinical course of sarcomas of extremities in newborn infants
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Diagnóstico Pré-Natal
/
Prognóstico
/
Recém-Nascido
/
Fatores de Risco
/
Rabdomiossarcoma Embrionário
Tipo de estudo:
Relato de Casos
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Iran. J. Pediatr.
Ano de publicação:
2008
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