User talk:Eldaverino

My 2 year grandson has been undertaken USG guided biopsy from "abdominopelvic solid mass" shows scanty fragments of a spindle cell tumor lying in a myxoid matrix. The tumor cells are immunopositive for myogenin. WTI (cytoplasmic) mic-2 (CD99), desmin (occasional cell) and S100 (occasional cell). Histological features are suggestive of a spindle cell variant of embryonal rhabdomyosarcoma. Note from Pathology: Given the limitation of a needle biopsy, an extratrenal Wilms' tumor was considered in the differential diagnosis. However the cytoplasmic WT1 (N-terminal clone) and stong myogenic marker positivity favour a diagnosis of an embryonal rhabdomyosarcoma.

Can you suggest me the treatment to be given to him ? Hospital where he can be treated in India only? Will it be cured at All India Institute of Medical Science New Delhi ?

Regards;

T S Negi