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Unusual Metastatic Patterns of Wilms Tumor: A Case Series.
Tagoe, Lily G; Bonney, Nana Yaa A; Amoako, Emmanuella; Amegan-Aho, Kokou H; Gbadamosi, Hafisatu; Dadzie, Mary-Ann; Segbefia, Catherine I.
Afiliação
  • Tagoe LG; Child Health, Korle Bu Teaching Hospital, Accra, GHA.
  • Bonney NYA; Child Health, Korle Bu Teaching Hospital, Accra, GHA.
  • Amoako E; Child Health, Korle Bu Teaching Hospital, Accra, GHA.
  • Amegan-Aho KH; Pediatrics and Child Health, University of Health and Allied Sciences, Ho, GHA.
  • Gbadamosi H; Radiology, Korle Bu Teaching Hospital, Accra, GHA.
  • Dadzie MA; Radiotherapy and Nuclear Medicine, Korle Bu Teaching Hospital, Accra, GHA.
  • Segbefia CI; Child Health, University of Ghana Medical School, Accra, GHA.
Cureus ; 16(2): e54640, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38523916
ABSTRACT
Wilms tumor (WT) is the most common renal malignancy of childhood. The common metastatic sites are the lungs, liver, and lymph nodes, with brain and bone metastases occurring rarely. Metastatic disease can be present at initial diagnosis or may occur with relapse or disease progression. The majority of relapses in WT occur within the first two years post-treatment. Late relapses are rare. This article describes four cases of WT, each demonstrating an unusual site or timing of metastases. Case 1 presented primarily with jaw metastases, Case 2 presented with bone (vertebrae) and spinal metastases manifesting as paraplegia, at relapse one year after completion of treatment, Case 3 presented with isolated liver metastases four years after treatment completion, and Case 4 presented with brain metastases after six weeks of treatment abandonment. This case series demonstrates the varied pattern of metastases of WT and highlights the need for a high index of suspicion for WT among patients who present with unusual sites of tumor or for metastasis in those who present with neurologic symptoms during or after treatment.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article