Difference between revisions of "Renal oncocytosis"
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==Molecular== | ==Molecular== | ||
*Scant data suggests chromosomal changes are different than those of [[ChRCC]] and [[oncocytoma]].<ref name=pmid20305535>{{Cite journal | last1 = Gobbo | first1 = S. | last2 = Eble | first2 = JN. | last3 = Delahunt | first3 = B. | last4 = Grignon | first4 = DJ. | last5 = Samaratunga | first5 = H. | last6 = Martignoni | first6 = G. | last7 = Zhang | first7 = S. | last8 = Wang | first8 = M. | last9 = Brunelli | first9 = M. | title = Renal cell neoplasms of oncocytosis have distinct morphologic, immunohistochemical, and cytogenetic profiles. | journal = Am J Surg Pathol | volume = 34 | issue = 5 | pages = 620-6 | month = May | year = 2010 | doi = 10.1097/PAS.0b013e3181d73293 | PMID = 20305535 }}</ref> | *Scant data suggests chromosomal changes are seen that are different than those of [[ChRCC]] and [[oncocytoma]].<ref name=pmid20305535>{{Cite journal | last1 = Gobbo | first1 = S. | last2 = Eble | first2 = JN. | last3 = Delahunt | first3 = B. | last4 = Grignon | first4 = DJ. | last5 = Samaratunga | first5 = H. | last6 = Martignoni | first6 = G. | last7 = Zhang | first7 = S. | last8 = Wang | first8 = M. | last9 = Brunelli | first9 = M. | title = Renal cell neoplasms of oncocytosis have distinct morphologic, immunohistochemical, and cytogenetic profiles. | journal = Am J Surg Pathol | volume = 34 | issue = 5 | pages = 620-6 | month = May | year = 2010 | doi = 10.1097/PAS.0b013e3181d73293 | PMID = 20305535 }}</ref> | ||
==See also== | ==See also== | ||
Revision as of 04:26, 4 December 2015
| Renal oncocytosis | |
|---|---|
| Diagnosis in short | |
|
| |
| LM | any mixture of oncocytic tumours - see hybrid tumour, chromophobe renal cell carcinoma and renal oncocytoma |
| LM DDx | other renal tumours with eosinophilic cytoplasm |
| IHC | characteristic of the histologic appearance - stain like oncocytoma, ChRCC and hybrid tumour |
| Gross | multiple brown kidney nodules (bilateral or unilateral) |
| Grossing notes | total nephrectomy for tumour grossing, partial nephrectomy grossing |
| Staging | kidney cancer staging |
| Site | kidney - see kidney tumours |
|
| |
| Syndromes | Birt–Hogg–Dubé syndrome |
|
| |
| Clinical history | +/-chronic renal failure and hemodialysis |
| Prevalence | rare |
| Radiology | multiple renal tumours (unilateral or bilateral) |
| Clin. DDx | metastatic disease, multifocal renal cell carcinoma |
Renal oncocytosis is the presence of multiple oncocytic lesions within the kidney.[1]
General
- Rare.
- May be seen in the context of Birt–Hogg–Dubé syndrome or chronic renal failure or may be sporadic.[1]
- Chronic renal failure seen in 50% of cases in one series.[2]
Gross
- Multiple (unilateral or bilateral) brown-coloured nodules.[1]
Microscopic
Features:
- Any mixture of oncocytic tumours (hybrid tumour, chromophobe renal cell carcinoma, renal oncocytoma).
DDx:
- Hybrid tumour.
- Chromophobe renal cell carcinoma.
- Renal oncocytoma.
- Other renal tumours with eosinophilic cytoplasm.
IHC
- Characteristic of the histologic appearance.[1]
- Stain like renal oncocytomas, chromophobe renal cell carcinomas and hybrid tumours.
Molecular
- Scant data suggests chromosomal changes are seen that are different than those of ChRCC and oncocytoma.[3]
See also
References
- ↑ 1.0 1.1 1.2 1.3 Kuroda, N.; Tanaka, A.; Ohe, C.; Mikami, S.; Nagashima, Y.; Sasaki, T.; Inoue, K.; Hes, O. et al. (Nov 2012). "Review of renal oncocytosis (multiple oncocytic lesions) with focus on clinical and pathobiological aspects.". Histol Histopathol 27 (11): 1407-12. PMID 23018240.
- ↑ Adamy, A.; Lowrance, WT.; Yee, DS.; Chong, KT.; Bernstein, M.; Tickoo, SK.; Coleman, JA.; Russo, P. (Mar 2011). "Renal oncocytosis: management and clinical outcomes.". J Urol 185 (3): 795-801. doi:10.1016/j.juro.2010.10.068. PMID 21239013.
- ↑ Gobbo, S.; Eble, JN.; Delahunt, B.; Grignon, DJ.; Samaratunga, H.; Martignoni, G.; Zhang, S.; Wang, M. et al. (May 2010). "Renal cell neoplasms of oncocytosis have distinct morphologic, immunohistochemical, and cytogenetic profiles.". Am J Surg Pathol 34 (5): 620-6. doi:10.1097/PAS.0b013e3181d73293. PMID 20305535.