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Structured assessment and followup for patients with hereditary kidney tumour syndromes
Author(s) -
JeanBaptiste Lattouf,
Stephen E. Pautler,
M. Neil Reaume,
Raymond H. Kim,
Melanie Care,
Jane Green,
Alan So,
Philippe D. Violette,
Issam Saliba,
Philippe Major,
Shane Silver,
Richard Leicht,
Joan Basiuk,
Simon Tanguay,
Michael A.S. Jewett,
Darrel Drachenberg
Publication year - 2016
Publication title -
canadian urological association journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.477
H-Index - 38
eISSN - 1920-1214
pISSN - 1911-6470
DOI - 10.5489/cuaj.3798
Subject(s) - medicine , tuberous sclerosis , renal cell carcinoma , leiomyomatosis , kidney cancer , von hippel–lindau disease , pheochromocytoma , disease , oncology , gynecology , surgery , pathology , leiomyoma
Optimal clinical assessment and subsequent followup of patients with or suspected of having a hereditary renal cell carcinoma syndrome (hRCC) is not standardized and practice varies widely. We propose protocols to optimize these processes in patients with hRCC to encourage a more uniform approach to management that can then be evaluated.

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