Literature DB >> 22876716

Primary gastric rhabdomyosarcoma. Case report.

Mariano Palermo1, Luis M Mastronardi, Rafael H García, Ignacio Solari, Francisco J Tarsitano.   

Abstract

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.

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Year:  2012        PMID: 22876716

Source DB:  PubMed          Journal:  Acta Gastroenterol Latinoam        ISSN: 0300-9033


  2 in total

1.  An Exceptionally Rare Primary Epithelioid Rhabdomyosarcomas of the Stomach: A Case Report.

Authors:  Lav Kumar Shah; Nashruva Jahan Mony; Sumitanand Mishra; Biswas Pant
Journal:  Cureus       Date:  2022-06-17

Review 2.  Primary epithelioid rhabdomyosarcoma of the stomach: a case report and review of literature.

Authors:  Yangkun Wang; Pei Guo; Zhishang Zhang; Runde Jiang; Zuguo Li
Journal:  Diagn Pathol       Date:  2019-12-23       Impact factor: 2.644

  2 in total

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