UTERINE RHABDOMYOSARCOMA

Authors

  • Waldemar Augusto Rivoire
  • Heleusa Ione Monego
  • Márcia Appel
  • Ricardo dos Reis
  • Luiz Augusto L. da Costa
  • Edison Capp

DOI:

https://doi.org/10.22491/2357-9730.126144

Keywords:

Rhabdomyosarcoma, uterine sarcoma, cancer, uterine bleeding

Abstract

Uterine rhabdomyosarcomas are very rare. They are characterized by late diagnosis and poor prognosis. In this paper we report clinical manifestations of this tumor in a 37-year-old patient. Rhabdomyosarcomas are treated similarly to endometrial sarcomas. The initial therapy for most uterine sarcomas is exploratory laparotomy, total abdominal hysterectomy, and bilateral salpingo-oophorectomy. There is not much information about the epidemiologic risk factors for sarcoma; similarly, little work has been performed assessing molecular alterations in sarcomas. Because of their rarity, uterine sarcomas are not suitable for screening. They are best managed by specialists with expertise in these malignancies, but primary care physicians can play an important role in the early diagnosis. In suspected cases, endometrial biopsy or dilation and curettage may aid diagnosis.

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Published

2022-07-27

How to Cite

1.
Rivoire WA, Monego HI, Appel M, dos Reis R, L. da Costa LA, Capp E. UTERINE RHABDOMYOSARCOMA. Clin Biomed Res [Internet]. 2022 Jul. 27 [cited 2026 Oct. 9];22(2). Available from: https://seer.ufrgs.br/index.php/hcpa/article/view/126144

Issue

Section

Case Report

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