Hereditary renal cancer syndromes
Updates to Article Attributes
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was changed:
Despite the vast majority of renal cancers being sporadic, there are a number of hereditary renal cancer syndromes:
- von Hippel Lindau syndrome: predominantly clear cell type
- tuberous sclerosis: predominantly clear cell type
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hereditary
leiomyomataleiomyomatosis and renal cellcancer syndromecarcinoma: described in ISUP Vancouver classification32 - Birt-Hogg-Dube syndrome: predominantly chromophobe renal cell cancer (also associated with oncocytic adenomas)
- hereditary papillary renal cell cancer type 1: papillary type I
- hereditary non-polyposis colon cancer (Lynch type II): predominantly transitional cell carcinoma of the renal pelvis
- hereditary renal oncocytoma
- sickle cell anaemia: medullary renal carcinoma
See also
-<a href="/articles/hereditary-leiomyomata-renal-cell-cancer-syndrome-hlrcc">hereditary leiomyomata renal cell cancer syndrome</a>: described in ISUP Vancouver classification <sup>3</sup>- +<a title="Hereditary leiomyomatosis and renal cell carcinoma" href="/articles/hereditary-leiomyomatosis-and-renal-cell-carcinoma">hereditary leiomyomatosis and renal cell carcinoma</a> <sup>2</sup>
References changed:
- 3. Srigley JR, Delahunt B, Eble JN et-al. The International Society of Urological Pathology (ISUP) Vancouver Classification of Renal Neoplasia. Am. J. Surg. Pathol. 2013;37 (10): 1469-89. <a href="http://dx.doi.org/10.1097/PAS.0b013e318299f2d1">doi:10.1097/PAS.0b013e318299f2d1</a> - <a href="http://www.ncbi.nlm.nih.gov/pubmed/24025519">Pubmed citation</a><span class="auto"></span>