A Case of Orbital Rhabdomyosarcoma
Journal of the Korean Ophthalmological Society
;
: 691-695, 1990.
Artigo
em Coreano
| WPRIM
| ID: wpr-29355
ABSTRACT
The orbital rhabdomyosarcoma is the most common primary malignant tumor of the orbit in childhood. It was first described in 1854 by Weber and has been increased possibly due to improvement of diagnostic procedures. A 7-year-old boy with the complaints of proptosis and visual disturbance coincidently had an ocular trauma. Incision and drainage of intraorbital hematoma was performed in the right orbit which was confirmed with orbital CT scan. Microscopic findings showed ovoid and spindle shaped rhabdoblasts, hyperchromatic nuclei, and characteristic cross striation in the cytoplasm of the giant cells. He was diagnosed as embryonal rhabdomyosarcoma. The intraorbital hematoma and surrounding tissue in the right orbit were excised and the right eye was enucleated. He received chemotherapy and radiation therapy.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Órbita
/
Rabdomiossarcoma
/
Tomografia Computadorizada por Raios X
/
Células Gigantes
/
Drenagem
/
Exoftalmia
/
Rabdomiossarcoma Embrionário
/
Citoplasma
/
Tratamento Farmacológico
/
Hematoma
Limite:
Criança
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1990
Tipo de documento:
Artigo
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