Cystic nephroma overview: Difference between revisions
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There is no classification system established for cystic nephroma. | There is no classification system established for cystic nephroma. | ||
==Pathophysiology== | |||
On gross pathology, large, unilateral, multiloculated, and well-encapsulated [[cystic]] [[tumor]] is the characteristic finding of cystic nephroma. On microscopic histopathological analysis, [[cyst]]s lined by a simple [[epithelium]] with a hobnail morphology and [[ovary|ovarian]]-like [[stroma]] are characteristic findings of cystic nephroma. | |||
==Causes== | |||
Cystic nephroma is caused by mutations in the [[DICER1]] gene.<ref name="pmid24481001">{{cite journal |vauthors=Doros LA, Rossi CT, Yang J, Field A, Williams GM, Messinger Y, Cajaiba MM, Perlman EJ, A Schultz K, Cathro HP, Legallo RD, LaFortune KA, Chikwava KR, Faria P, Geller JI, Dome JS, Mullen EA, Gratias EJ, Dehner LP, Hill DA |title=DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma |journal=[[Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc]] |volume=27 |issue=9 |pages=1267–80 |year=2014 |pmid=24481001 |pmc=4117822 |doi=10.1038/modpathol.2013.242 |url=http://dx.doi.org/10.1038/modpathol.2013.242}}</ref> | |||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shanshan Cen, M.D. [2]
Overview
Cystic nephroma is a type of rare benign kidney tumor.[1]
Classification
There is no classification system established for cystic nephroma.
Pathophysiology
On gross pathology, large, unilateral, multiloculated, and well-encapsulated cystic tumor is the characteristic finding of cystic nephroma. On microscopic histopathological analysis, cysts lined by a simple epithelium with a hobnail morphology and ovarian-like stroma are characteristic findings of cystic nephroma.
Causes
Cystic nephroma is caused by mutations in the DICER1 gene.[2]
References
- ↑ Turbiner J, Amin MB, Humphrey PA, et al. (April 2007). "Cystic nephroma and mixed epithelial and stromal tumor of kidney: a detailed clinicopathologic analysis of 34 cases and proposal for renal epithelial and stromal tumor (REST) as a unifying term". Am. J. Surg. Pathol. 31 (4): 489–500. doi:10.1097/PAS.0b013e31802bdd56. PMID 17414095.
- ↑ Doros LA, Rossi CT, Yang J, Field A, Williams GM, Messinger Y, Cajaiba MM, Perlman EJ, A Schultz K, Cathro HP, Legallo RD, LaFortune KA, Chikwava KR, Faria P, Geller JI, Dome JS, Mullen EA, Gratias EJ, Dehner LP, Hill DA (2014). "DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma". Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc. 27 (9): 1267–80. doi:10.1038/modpathol.2013.242. PMC 4117822. PMID 24481001.