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10.1136/bcr-2015-209771

http://scihub22266oqcxt.onion/10.1136/bcr-2015-209771
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C4401955!4401955 !25878237
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suck abstract from ncbi


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pmid25878237
      BMJ+Case+Rep 2015 ; 2015 (ä): ä
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  • A rare case of bilateral cystic partially differentiated nephroblastoma recurring as bilateral cystic Wilms tumour #MMPMID25878237
  • Kurian JJ ; Ninan PJ
  • BMJ Case Rep 2015[Apr]; 2015 (ä): ä PMID25878237 show ga
  • Childhood cystic partially differentiated nephroblastoma (CPDN) is an uncommon renal neoplasm. Bilateral CPDN or CPDN co-existing with a cystic nephroma/Wilms tumour is extremely rare. Treatment of CPDN is by complete surgical excision. Although local recurrences are uncommon, distant metastases have not been described. We present a case of bilateral CPDN that, after complete excision, recurred as bilateral cystic Wilms tumour. To the best of our knowledge, this is the first reported case in the literature where a bilateral CPDN has recurred as bilateral Wilms tumour.
  • |Diagnosis, Differential [MESH]
  • |Humans [MESH]
  • |Infant [MESH]
  • |Male [MESH]
  • |Neoplasm Recurrence, Local/*pathology/surgery [MESH]
  • |Polycystic Kidney Diseases/*diagnosis/diagnostic imaging/*pathology [MESH]
  • |Radiography [MESH]


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