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Difference between revisions of "Succinate dehydrogenase-deficient renal cell carcinoma"
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Succinate dehydrogenase-deficient renal cell carcinoma (view source)
Revision as of 05:00, 12 May 2015
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==General== | ==General== | ||
*Extremely rare - | *Extremely rare - estimated to represent up to 0.2% of [[renal cell carcinoma]]s.<ref name=pmid25025441>{{Cite journal | last1 = Gill | first1 = AJ. | last2 = Hes | first2 = O. | last3 = Papathomas | first3 = T. | last4 = Šedivcová | first4 = M. | last5 = Tan | first5 = PH. | last6 = Agaimy | first6 = A. | last7 = Andresen | first7 = PA. | last8 = Kedziora | first8 = A. | last9 = Clarkson | first9 = A. | title = Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients. | journal = Am J Surg Pathol | volume = 38 | issue = 12 | pages = 1588-602 | month = Dec | year = 2014 | doi = 10.1097/PAS.0000000000000292 | PMID = 25025441 }}</ref> | ||
*May be assocated with [[paraganglioma]] and familial, as with several SDH mutations.<ref name=pmid25800244>{{Cite journal | last1 = Hernandez | first1 = KG. | last2 = Ezzat | first2 = S. | last3 = Morel | first3 = CF. | last4 = Swallow | first4 = C. | last5 = Otremba | first5 = M. | last6 = Dickson | first6 = BC. | last7 = Asa | first7 = SL. | last8 = Mete | first8 = O. | title = Familial pheochromocytoma and renal cell carcinoma syndrome: TMEM127 as a novel candidate gene for the association. | journal = Virchows Arch | volume = | issue = | pages = | month = Mar | year = 2015 | doi = 10.1007/s00428-015-1755-2 | PMID = 25800244 }}</ref> | *May be assocated with [[paraganglioma]] and familial, as with several SDH mutations.<ref name=pmid25800244>{{Cite journal | last1 = Hernandez | first1 = KG. | last2 = Ezzat | first2 = S. | last3 = Morel | first3 = CF. | last4 = Swallow | first4 = C. | last5 = Otremba | first5 = M. | last6 = Dickson | first6 = BC. | last7 = Asa | first7 = SL. | last8 = Mete | first8 = O. | title = Familial pheochromocytoma and renal cell carcinoma syndrome: TMEM127 as a novel candidate gene for the association. | journal = Virchows Arch | volume = | issue = | pages = | month = Mar | year = 2015 | doi = 10.1007/s00428-015-1755-2 | PMID = 25800244 }}</ref> | ||
*Primarily described with a ''SDHB mutation''.<ref name=pmid25034258/> | *Primarily described with a ''SDHB mutation''.<ref name=pmid25034258/> | ||