Case report of an infant with congenital mesoblastic nephroma leading to pulmonary metastasis

Author:

Athapathu Arjuna Salinda123,Wijayawardhana Sameera M4ORCID,Meegoda Jithmal5,Gunaratne Sandini A6,Somathilaka Mahendra7,Chang Kenneth Tou En8,Wickramasinghe Pujitha39

Affiliation:

1. Faculty of Medicine, Department of Paediatrics, University of Kelaniya, Ragama, Sri Lanka

2. Postgraduate Institute of Medicine, University of Colombo, Colombo, Sri Lanka

3. University Paediatrics Unit, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka

4. Faculty of Medicine, Department of Anatomy, University of Kelaniya, Ragama, Sri Lanka

5. Faculty of Medicine, Department of Pathology, University of Colombo, Colombo, Sri Lanka

6. Department of Histopathology, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka

7. National Cancer Institute, Maharagama, Sri Lanka

8. Department of Pathology and Laboratory Medicine, KK Women’s and Children’s Hospital, Singapore

9. Faculty of Medicine, Department of Paediatrics, University of Colombo, Colombo, Sri Lanka

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.

Publisher

SAGE Publications

Subject

General Medicine

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