Hereditary renal cancer syndromes
Updates to Article Attributes
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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 (also associated with angiomyolipoma)
- hereditary paraganglioma-pheochromocytoma syndromes: predominantly clear cell type
- hereditary papillary renal cell carcinoma: papillary type 1
- hereditary leiomyomatosis and renal cell carcinoma: predominantly papillary type 2
- Birt-Hogg-Dubé syndrome: predominantly chromophobe type, oncocytoma, or a hybrid of both
- hereditary non-polyposis colon cancer (Lynch type II): predominantly upper tract urothelial carcinoma
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sickle cell trait
traitorhemoglobinhaemoglobin SC disease: renal medullary carcinoma - hereditary renal oncocytoma: oncocytoma
See also
-<a href="/articles/sickle-cell-disease">sickle cell</a> trait or hemoglobin SC disease: <a href="/articles/renal-medullary-carcinoma">renal medullary carcinoma</a>- +<a title="sickle cell trait" href="/articles/sickle-cell-trait">sickle cell trait</a> or <a title="Haemoglobin SC disease" href="/articles/haemoglobin-sc-disease">haemoglobin SC disease</a>: <a href="/articles/renal-medullary-carcinoma">renal medullary carcinoma</a>