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Rare case of blastemal predominant adult Wilms’ tumor with skeletal metastasis case report and brief review of literature

Wilms’ tumor (nephroblastoma) is extremely rare in adults, skeletal metastasis being still rarer. The clinical course of adult Wilms’ tumor is very aggressive. The present case is a rare blastemal predominant adult Wilms’ tumor presenting with skeletal metastasis. We report a case of 19-year-old fem...

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Detaylı Bibliyografya
Asıl Yazarlar: Patnayak, Rashmi, Rambabu, D. V. S., Jena, Amitabh, Vijaylaxmi, Bodagala, Phaneendra, B. V., Reddy, M. Kumaraswamy
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2012
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3579131/
https://ncbi.nlm.nih.gov/pubmed/23450214
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0970-1591.105772
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