Your browser doesn't support javascript.
loading
Case report of an infant with congenital mesoblastic nephroma leading to pulmonary metastasis.
Athapathu, Arjuna Salinda; Wijayawardhana, Sameera M; Meegoda, Jithmal; Gunaratne, Sandini A; Somathilaka, Mahendra; Chang, Kenneth Tou En; Wickramasinghe, Pujitha.
Afiliación
  • Athapathu AS; Faculty of Medicine, Department of Paediatrics, University of Kelaniya, Ragama, Sri Lanka.
  • Wijayawardhana SM; Postgraduate Institute of Medicine, University of Colombo, Colombo, Sri Lanka.
  • Meegoda J; University Paediatrics Unit, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka.
  • Gunaratne SA; Faculty of Medicine, Department of Anatomy, University of Kelaniya, Ragama, Sri Lanka.
  • Somathilaka M; Faculty of Medicine, Department of Pathology, University of Colombo, Colombo, Sri Lanka.
  • Chang KTE; Department of Histopathology, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka.
  • Wickramasinghe P; National Cancer Institute, Maharagama, Sri Lanka.
SAGE Open Med Case Rep ; 11: 2050313X231220826, 2023.
Article en En | MEDLINE | ID: mdl-38149118
ABSTRACT
Congenital mesoblastic nephroma is considered a tumour with favourable clinical behaviour with only few reported cases of metastases. We report an infant who underwent complete resection and later developed pulmonary metastasis. Ten-month-old baby girl initially presented at 3 weeks of age with macroscopic haematuria, hypertension and a lumbar mass. Contrast-enhanced computed tomography revealed a tumour arising from the left kidney without local invasion or metastasis. She underwent left nephrectomy. Immunohistochemistry confirmed a cellular type of congenital mesoblastic nephroma. At 10 months, she presented with difficulty in breathing. Contrast-enhanced computed tomography revealed an opacity in the right hemi-thorax. Histology of lung mass was suggestive of deposits from the previously excised mesoblastic nephroma. She developed a right-sided haemothorax and succumbed. This case report highlights the fact that even though congenital mesoblastic nephromas are considered tumours with favourable clinical behaviour, they can present later with distant metastasis. Therefore, clinicians need to be aware of this rare malignant potential and adhere to meticulous follow-up protocols.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: SAGE Open Med Case Rep Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: SAGE Open Med Case Rep Año: 2023 Tipo del documento: Article