An Atypical Presentation of Rhabdomyosarcoma

Date of submission: 25-11-2019 | Date of acceptance: 20-02-2020 | Published: 02-10-2020

Authors

  • Mariana Morgado Pediatric Surgery Department, Hospital de Santa Maria, Lisboa, Portugal
  • Maria João Palaré Pediatrics Department, Hospital de Santa Maria, Lisboa, Portugal
  • Luísa Lobo Radiology Department, Hospital de Santa Maria, Lisboa, Portugal
  • Miroslava Gonçalves Pediatric Surgery Department, Hospital de Santa Maria, Lisboa, Portugal

DOI:

https://doi.org/10.25754/pjp.2020.18944

Abstract

Thromboembolism is infrequent in children, nonetheless, whenever malignancy is present, there is an increased risk, around 7% to 25%. Rhabdomyosarcomas are typically asymptomatic masses, but patients can become symptomatic due to mass overgrowth and compression of surrounding structures, therefore presentation might be as a thromboembolic event. Sarcomas have recognized risk factors including large tumour masses, intensive chemotherapy, radiation therapy, extensive surgery and associated limited mobility. Whenever a thromboembolic event presents without a reliable aetiology and with no response to conventional treatment, an underlying malignancy should be excluded. In this context, we present a six-year-old boy who presented with a persistent symptomatic deep venous thrombosis of the inferior limb, despite anticoagulation and, in the subsequent investigation, a retroperitoneal rhabdomyosarcoma was diagnosed. In the light of this case, a brief review of the literature review is presented.

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Published

2020-10-15

Issue

Section

Case reports

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