Literature DB >> 17414095

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.

Julia Turbiner1, Mahul B Amin, Peter A Humphrey, John R Srigley, Laurence De Leval, Anuradha Radhakrishnan, Esther Oliva.   

Abstract

Cystic nephroma (CN) and mixed epithelial and stromal tumor (MEST) are rare benign renal neoplasms that have overlapping clinical and morphologic features, including predominance in middle-aged women, variably cystic architecture, eosinophilic cells, and hobnail cells lining the cysts and ovarian-type stroma. The aim of this study was to analyze and compare the histologic features and immunohistochemical profile of these tumors. We studied 34 cases from 5 large academic institutions. Twenty tumors were diagnosed as CNs, 18 in women and 2 in men, their age ranged from 24 to 63 (mean 48; median 50) years. Fourteen tumors were diagnosed as MESTs, all in women, their age ranged from 26 to 84 (mean 52; median 51) years. Histologically, all tumors were well-circumscribed except for one MEST. The stromal/epithelial ratio was approximately 2.3 in MESTs versus 0.3 in CNs; cellular ovarian-type stroma composed 45% of the stroma in MESTs and 12% of the stroma of CNs. Stromal hyalinization was prominent in both. Five MESTs showed stromal luteinization. In the epithelial component, the relative amount of large cysts, medium to small cysts, and phyllodes-type glands was: 65%/25%/10% in CNs versus 25%/40%/35% in MESTs. The epithelial component ranged from flat to cuboidal to hobnail cells in both types of tumors. No significant atypia of either component was seen, although the epithelial cells showed reactive changes. Immunohistochemical stains for estrogen receptors and progesterone receptors showed 62% and 85% positivity in the stromal component of MESTs versus 19% and 40% in CNs. CD10 positivity was seen in 77% of MESTs versus 50% of CNs, calretinin was seen in 69% of MESTs versus 41% of CNs, and inhibin in 42% of MESTs versus 36% of CNs, although the staining was focal. Follow-up in both categories of tumors (mean 3.2 y, median 3 y for CNs and mean 2.5 y, median of 2 y for MESTs) showed no evidence of recurrence or metastases in keeping with their benign nature. This study highlights the remarkable similarity between CN and MEST in sex predilection, age distribution, and morphologic attributes of both the epithelial and stromal components and immunohistochemical profile albeit with variation in individual categories with higher prevalence of stromal to epithelial ratio, prominent ovarian stroma, smaller cysts with phyllodes glands pattern and stromal luteinization being more common in MEST; and large cysts, thin septae and low stromal to epithelial ratio in CN. The presence of ovarian-type stroma and müllerian related immunohistochemical markers raises the possibility that these tumors may originate from müllerian remnants misplaced during embryogenesis. On the basis of detailed morphologic analysis of this series of CN and MEST, we propose a unifying term of "renal epithelial and stromal tumor" (REST) to encompass the spectrum of findings observed in these tumors at least until new molecular studies can prove or disprove this challenging hypothesis.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17414095     DOI: 10.1097/PAS.0b013e31802bdd56

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  36 in total

1.  High-resolution genomic profiling of an adult Wilms' tumor: evidence for a pathogenesis distinct from corresponding pediatric tumors.

Authors:  Jenny Karlsson; Linda Holmquist Mengelbier; Peter Elfving; David Gisselsson Nord
Journal:  Virchows Arch       Date:  2011-09-23       Impact factor: 4.064

2.  Case report: a left upper quadrant complex cystic mass.

Authors:  Lydia Choi; Neena Mirani; Steve H Kim
Journal:  Int J Surg Case Rep       Date:  2011-11-10

3.  Exophytic benign mixed epithelial stromal tumour of the kidney: case report of a rare tumour entity.

Authors:  Michael Richter; Werner Meyer; Jens Küster; Peter Middel
Journal:  Diagn Pathol       Date:  2010-03-01       Impact factor: 2.644

4.  Mixed epithelial and stromal tumors of the kidney discovered incidentally at autopsy.

Authors:  Varsha Podduturi; Joseph M Guileyardo
Journal:  Proc (Bayl Univ Med Cent)       Date:  2015-04

Review 5.  Mixed epithelial and stromal tumor of the kidney: report of a rare case and review of literature.

Authors:  Ying Wang; Junqing Yuan; Jihong Wang; Qiang Fu
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01

6.  Giant Renal Mixed Epithelial and Stromal Tumour in A Young Female: A Rare Presentation.

Authors:  Sidhartha Kalra; Ramanitharan Manikandan; Lalgudi Narayanan Dorairajan
Journal:  J Clin Diagn Res       Date:  2015-05-01

7.  Tubulocystic carcinoma of the kidney: a histologic, immunohistochemical, and ultrastructural study.

Authors:  Borislav A Alexiev; Cinthia B Drachenberg
Journal:  Virchows Arch       Date:  2013-03-24       Impact factor: 4.064

Review 8.  Malignant mixed epithelial and stromal tumor of the kidney: the second male case and review of literature.

Authors:  Liang Zou; Xiuming Zhang; Hua Xiang
Journal:  Int J Clin Exp Pathol       Date:  2014-04-15

9.  Mixed epithelial and stromal tumour of the kidney.

Authors:  Eric Simpson; Shalini Koppisetty; Ricardo C Alessio; Anil Kumar
Journal:  BMJ Case Rep       Date:  2015-07-27

10.  Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations.

Authors:  Mariana M Cajaiba; Geetika Khanna; Ethan A Smith; Lan Gellert; Yueh-Yun Chi; Elizabeth A Mullen; Dana A Hill; James I Geller; Jeffrey S Dome; Elizabeth J Perlman
Journal:  Hum Pathol       Date:  2015-10-28       Impact factor: 3.466

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.