Difference between revisions of "Succinate dehydrogenase-deficient renal cell carcinoma"
		
		
		
		
		
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Others:  | Others:  | ||
*PAX8 +ve.  | *PAX8 +ve.  | ||
*EMA +ve (10/10<ref name=pmid25034258/>).  | |||
*CK7 -ve (1/35).  | *CK7 -ve (1/35).  | ||
*AE1/AE3 -ve/+ve (4 +ve/10<ref name=pmidpmid25034258/>).  | |||
==See also==  | ==See also==  | ||
Revision as of 23:01, 4 May 2015
| Succinate dehydrogenase-deficient renal cell carcinoma | |
|---|---|
| Diagnosis in short | |
| 
 SDH-deficient renal cell carcinoma. H&E stain.  | |
| 
 | |
| LM | eosinophilic cells with clear (flocculent) cytoplasmic inclusions, round nuclei with mildly granular chromatin pattern, intratumoural mast cells, solid architecture | 
| LM DDx | renal oncocytoma, chromophobe renal cell carcinoma, clear cell renal cell carcinoma, other renal tumours with eosinophilic cytoplasm | 
| Stains | SDHB -ve, CK7 -ve, CD117 -ve, PAX8 +ve | 
| Gross | mass lesion, commonly cystic | 
| Site | kidney - see kidney tumours | 
| 
 | |
| Syndromes | familial pheochromocytoma and renal cell carcinoma syndrome | 
| 
 | |
| Prevalence | extremely rare | 
| Prognosis | usually good prognosis (limited data) | 
| Clin. DDx | other kidney tumours | 
Succinate dehydrogenase-deficient renal cell carcinoma, also succinate dehydrogenase renal cell carcinoma (abbreviated SDH-RCC), is a very rare type of renal cell carcinoma.
It is grouped in the emerging entities of the Vancouver modification of the 2004 WHO classification of renal neoplasia.[1]
General
- Extremely rare - only approximately 10 cases described as of 2012.[1]
 - May be assocated with paraganglioma and familial (as with several SDH mutations).[2]
 - Primarily described with a SDHB mutation.[3]
 - Usually good prognosis.
 
Gross
- Commonly cystic.
 
Microscopic
Features:[3]
- Eosinophilic cells with clear (flocculent) cytoplasmic inclusions. ‡
 - Round nuclei with mildly granular chromatin pattern.
 - Intratumoural mast cells.
 - Solid architecture.
 
Notes:
- ‡ Occasional cells may look like signet ring cells.
 - Typically low ISUP nucleolar grade.
- May be sarcomatoid.
 
 
DDx:
- Renal oncocytoma - granular cytoplasm.
 - Chromophobe renal cell carcinoma.
 - Clear cell renal cell carcinoma.
 - Other renal tumours with eosinophilic cytoplasm.
 
Images
www:
- SDHB-RCC - poor quality histology image (nih.gov).[4]
 - SDHC-RCC (nih.gov).[4]
 - SDH-deficient RCC (nature.com).[3]
 
Case 1
Case 2
IHC
Features:
- SDHB -ve (11 of 11 cases[3]).
- Normal tubules +ve.
 - May be (pseudo)negative in clear cells (as few mitochondria).
 
 - CD117 -ve - important.
 
Others:
See also
References
- ↑ 1.0 1.1 Srigley, JR.; Delahunt, B.; Eble, JN.; Egevad, L.; Epstein, JI.; Grignon, D.; Hes, O.; Moch, H. et al. (Oct 2013). "The International Society of Urological Pathology (ISUP) Vancouver Classification of Renal Neoplasia.". Am J Surg Pathol 37 (10): 1469-89. doi:10.1097/PAS.0b013e318299f2d1. PMID 24025519.
 - ↑ Hernandez, KG.; Ezzat, S.; Morel, CF.; Swallow, C.; Otremba, M.; Dickson, BC.; Asa, SL.; Mete, O. (Mar 2015). "Familial pheochromocytoma and renal cell carcinoma syndrome: TMEM127 as a novel candidate gene for the association.". Virchows Arch. doi:10.1007/s00428-015-1755-2. PMID 25800244.
 - ↑ 3.0 3.1 3.2 3.3 3.4 3.5 Williamson, SR.; Eble, JN.; Amin, MB.; Gupta, NS.; Smith, SC.; Sholl, LM.; Montironi, R.; Hirsch, MS. et al. (Jan 2015). "Succinate dehydrogenase-deficient renal cell carcinoma: detailed characterization of 11 tumors defining a unique subtype of renal cell carcinoma.". Mod Pathol 28 (1):  80-94. doi:10.1038/modpathol.2014.86. PMID 25034258. Cite error: Invalid 
<ref>tag; name "pmid25034258" defined multiple times with different content - ↑ 4.0 4.1 4.2 Ricketts, CJ.; Shuch, B.; Vocke, CD.; Metwalli, AR.; Bratslavsky, G.; Middelton, L.; Yang, Y.; Wei, MH. et al. (Dec 2012). "Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer.". J Urol 188 (6): 2063-71. doi:10.1016/j.juro.2012.08.030. PMID 23083876.
 - ↑ Cite error: Invalid 
<ref>tag; no text was provided for refs namedpmidpmid25034258