1.
Eur J Gynaecol Oncol
; 34(4): 332-5, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24020141
RESUMO
Embryonal rhabdomyosarcoma (RMS) is a rare sarcoma that characteristically occurs in children. The current treatment protocols are based on trials performed in patients under 21 years of age. Embryonal RMS in women over 20 years of age is rare, and studies on treatments and outcomes are limited. The authors here in report a case of a 35-year-old woman with ectocervical RMS who was treated with radical hysterectomy followed by chemotherapy. She is currently disease-free. Based on a literature review, the authors recommend a surgical approach in combination with chemotherapy for treatment of embryonal RMS in adult patients.
Assuntos
Rabdomiossarcoma Embrionário/terapia , Neoplasias Uterinas/terapia , Adulto , Terapia Combinada , Feminino , Humanos , Rabdomiossarcoma Embrionário/patologia , Neoplasias Uterinas/patologia
2.
Hiroshima J Med Sci
; 33(1): 81-100, 1984 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-6480373