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Acta Gastroenterol Latinoam ; 42(2): 131-4, 2012 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-22876716

RESUMEN

Rhabdomyosarcomas are rare and malignant tumors. There have been reported two histological types of gastric rhabdomyosarcomas, the pleomorphic and embryonal cell types. We report the case of a 53-year-old male with endoscopic diagnosis of a Bormann type III ulcer which revealed a gastric primary rhabdomyosarcoma. Ultrasound showed two liver lesions, two hepatic pedicle lymph nodes and a huge primary gastric tumor. CT scan revealed a primary gastric tumor. The patient is submitted to a distal gastrectomy with a Billroth II reconstruction and a resection of the distal liver metastases at segment IV The patient was discharged uneventfully on the eighth postoperative day. The gold standard for a final diagnoses is the immuno-histochemical staining of the endoscopic biopsy. There is very little information on the results of chemotherapy and the surgical treatment is the best choice.


Asunto(s)
Neoplasias Hepáticas/secundario , Rabdomiosarcoma/patología , Rabdomiosarcoma/secundario , Neoplasias Gástricas/patología , Biopsia , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad
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