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Mesenchymal Kidney Tumors

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Kidney Cancer

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Abstract

Mesenchymal tumors involving the kidney include a wide range of benign and malignant tumors and are relatively rare compared to epithelial neoplasms. Within the last two decades, there have been major discoveries in the underlying genomic alterations that drive the neoplastic process in mesenchymal lesions of the kidney. Specifically, a variety of translocation-associated sarcomas have been described arising from the kidney, significantly expanding the differential diagnosis of mesenchymal tumors primary to the kidney. This chapter is devoted to the clinical, morphologic, immunohistochemical, and genomic alterations of mesenchymal tumors that primarily occur in adults, with discussion of the differential diagnosis of specific entities. In contrast to the childhood lesions, most of these entities occur primarily in somatic soft tissue sites, but are also described in the kidney and constitute an ever-increasing list that appear to have a predilection for this location. It must be recognized that many of the neoplasms reviewed also occur in children.

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References

  1. Risi E, Iacovelli R, Altavilla A, et al. Clinical and pathological features of primary neuroectodermal tumor/Ewing sarcoma of the kidney. Urology. 2013;82:382–6.

    Article  PubMed  Google Scholar 

  2. Murugan P, Rao P, Tamboli P, et al. Primary Ewing sarcoma / primitive neuroectodermal tumor of the kidney: a clinicopathologic study of 23 cases. Pathol Oncol Res. 2018;24(1):153–9.

    Article  CAS  PubMed  Google Scholar 

  3. Ozdemirli M, Fanburg-Smith JC, Hartmann DP, et al. Precursor B-lymphoblastic lymphoma presenting as a solitary bone tumor and mimicking Ewing’s sarcoma: a report of four cases and review of the literature. Am J Surg Pathol. 1998;22:795–804.

    Article  CAS  PubMed  Google Scholar 

  4. Ozdemirli M, Fanburg-Smith JC, Hartmann DP, et al. Differentiating lymphoblastic lymphoma and Ewing’s sarcoma: lymphocyte markers and gene rearrangement. Mod Pathol. 2001;14:1175–82.

    Article  CAS  PubMed  Google Scholar 

  5. Perlman EJ, Lumadue JA, Hawkins AL, et al. Primary cutaneous neuroendocrine tumors. Diagnostic use of cytogenetic and MIC2 analysis. Cancer Genet Cytogenet. 1995;82:30–4.

    Article  CAS  PubMed  Google Scholar 

  6. Lumadue JA, Askin FB, Perlman EJ. MIC2 analysis of small cell carcinoma. Am J Clin Pathol. 1994;102:692–4.

    Article  CAS  PubMed  Google Scholar 

  7. Folpe AL, Hill CE, Parham DM, et al. Immunohistochemical detection of FLI-1 protein expression: a study of 132 round cell tumors with emphasis on CD99-positive mimics of Ewing’s sarcoma/primitive neuroectodermal tumor. Am J Surg Pathol. 2000;24:1657–62.

    Article  CAS  PubMed  Google Scholar 

  8. Gerald WL, Ladanyi M, De Alava E, et al. Clinical, pathologic, and molecular spectrum of tumors associated with T(11;22)(P13;Q12): desmoplastic small round-cell tumor and its variants. J Clin Oncol. 1998;16:3028–36.

    Article  CAS  PubMed  Google Scholar 

  9. Devaney K, Abbondanzo SL, Shekitka KM, et al. MIC2 detection in tumors of bone and adjacent soft tissues. Clin Orthop Relat Res. 1995:176–87.

    Google Scholar 

  10. Granter SR, Renshaw AA, Fletcher CD, et al. CD99 reactivity in mesenchymal chondrosarcoma. Hum Pathol. 1996;27:1273–6.

    Article  CAS  PubMed  Google Scholar 

  11. Folpe AL, Goldblum JR, Rubin BP, et al. Morphologic and immunophenotypic diversity in Ewing family tumors: a study of 66 genetically confirmed cases. Am J Surg Pathol. 2005;29:1025–33.

    PubMed  Google Scholar 

  12. Yoshida A, Sekine S, Tsuta K, et al. NKX2.2 is a useful immunohistochemical marker for Ewing sarcoma. Am J Surg Pathol. 2012;36:993–9.

    Article  PubMed  Google Scholar 

  13. Hung YP, Fletcher CD, Hornick JL. Evaluation of NKX2-2 expression in round cell sarcomas and other tumors with EWSR1 rearrangement: imperfect specificity for Ewing sarcoma. Mod Pathol. 2016;29:370–80.

    Article  CAS  PubMed  Google Scholar 

  14. Ng TL, O’sullivan MJ, Pallen CJ, et al. Ewing sarcoma with novel translocation T(2;16) producing an in-frame fusion of FUS and FEV. J Mol Diagn. 2007;9:459–63.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Shing DC, Mcmullan DJ, Roberts P, et al. FUS/ERG gene fusions in Ewing’s tumors. Cancer Res. 2003;63:4568–76.

    CAS  PubMed  Google Scholar 

  16. Graham C, Chilton-Macneill S, Zielenska M, et al. The CIC-DUX4 fusion transcript is present in a subgroup of pediatric primitive round cell sarcomas. Hum Pathol. 2012;43:180–9.

    Article  CAS  PubMed  Google Scholar 

  17. Italiano A, Sung YS, Zhang L, et al. High prevalence of cic fusion with double-homeobox (DUX4) transcription factors in EWSR1-negative undifferentiated small blue round cell sarcomas. Genes Chromosomes Cancer. 2012;51:207–18.

    Article  CAS  PubMed  Google Scholar 

  18. Mangray S, Somers GR, He J, et al. Primary undifferentiated sarcoma of the kidney harboring a novel variant of CIC-DUX4 gene fusion. Am J Surg Pathol. 2016;40:1298–301.

    Article  PubMed  Google Scholar 

  19. Bergerat S, Barthelemy P, Mouracade P, et al. Primary CIC-DUX4 round cell sarcoma of the kidney: a treatment-refractory tumor with poor outcome. Pathol Res Pract. 2017;213:154–60.

    Article  PubMed  Google Scholar 

  20. Antonescu CR, Owosho AA, Zhang L, et al. Sarcomas with CIC-rearrangements are a distinct pathologic entity with aggressive outcome: a clinicopathologic and molecular study of 115 cases. Am J Surg Pathol. 2017;41:941–9.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Specht K, Sung YS, Zhang L, et al. Distinct transcriptional signature and immunoprofile of CIC-DUX4 fusion-positive round cell tumors compared to EWSR1-rearranged Ewing sarcomas: further evidence toward distinct pathologic entities. Genes Chromosomes Cancer. 2014;53:622–33.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Mangray S, Kelly D, Leguellec S, et al. Clinical, morphologic, immunohistochemical and molecular features of a series of primary renal CIC-rearranged sarcomas. Am J Surg Pathol. 2018;42(10):1360–9.

    Article  PubMed  Google Scholar 

  23. Pierron G, Tirode F, Lucchesi C, et al. A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion. Nat Genet. 2012;44:461–6.

    Article  CAS  PubMed  Google Scholar 

  24. Argani P, Kao YC, Zhang L, et al. Primary renal sarcomas with BCOR-CCNB3 gene fusion: a report of 2 cases showing histologic overlap with clear cell sarcoma of kidney, suggesting further link between BCOR-related sarcomas of the kidney and soft tissues. Am J Surg Pathol. 2017;41:1702–12.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Mirza M, Zamilpa I, Bunning J. Primary renal synovial sarcoma. Urology. 2008;72:716.. E711-712

    Article  PubMed  Google Scholar 

  26. Shannon BA, Murch A, Cohen RJ. Primary renal synovial sarcoma confirmed by cytogenetic analysis: a lesion distinct from sarcomatoid renal cell carcinoma. Arch Pathol Lab Med. 2005;129:238–40.

    PubMed  Google Scholar 

  27. Argani P, Faria PA, Epstein JI, et al. Primary renal synovial sarcoma: molecular and morphologic delineation of an entity previously included among embryonal sarcomas of the kidney. Am J Surg Pathol. 2000;24:1087–96.

    Article  CAS  PubMed  Google Scholar 

  28. Palau LM, Thu Pham T, Barnard N, et al. Primary synovial sarcoma of the kidney with rhabdoid features. Int J Surg Pathol. 2007;15:421–8.

    Article  CAS  Google Scholar 

  29. Chen PC, Chang YH, Yen CC, et al. Primary renal synovial sarcoma with inferior vena cava and right atrium invasion. Int J Urol. 2003;10:657–60.

    Article  PubMed  Google Scholar 

  30. Vesoulis Z, Rahmeh T, Nelson R, et al. Fine needle aspiration biopsy of primary renal synovial sarcoma. A case report. Acta Cytol. 2003;47:668–72.

    Article  PubMed  Google Scholar 

  31. Karafin M, Parwani AV, Netto GJ, et al. Diffuse expression of Pax2 and Pax8 in the cystic epithelium of mixed epithelial stromal tumor, angiomyolipoma with epithelial cysts, and primary renal synovial sarcoma: evidence supporting renal tubular differentiation. Am J Surg Pathol. 2011;35:1264–73.

    Article  PubMed  Google Scholar 

  32. Eklund MJ, Cundiff C, Shehata BM, et al. Desmoplastic small round cell tumor of the kidney with unusual imaging features. Clin Imaging. 2015;39:904–7.

    Article  PubMed  Google Scholar 

  33. Egloff AM, Lee EY, Dillon JE, et al. Desmoplastic small round cell tumor of the kidney in a pediatric patient: sonographic and multiphase CT findings. AJR Am J Roentgenol. 2005;185:1347–9.

    Article  PubMed  Google Scholar 

  34. Eaton SH, Cendron MA. Primary desmoplastic small round cell tumor of the kidney in a 7-year-old girl. J Pediatr Urol. 2006;2:52–4.

    Article  PubMed  Google Scholar 

  35. Wang LL, Perlman EJ, Vujanic GM, et al. Desmoplastic small round cell tumor of the kidney in childhood. Am J Surg Pathol. 2007;31:576–84.

    Article  PubMed  Google Scholar 

  36. Walton WJ, Flores RR. Desmoplastic small round cell tumor of the kidney: AIRP best cases in radiologic-pathologic correlation. Radiographics. 2016;36:1533–8.

    Article  PubMed  Google Scholar 

  37. Su MC, Jeng YM, Chu YC. Desmoplastic small round cell tumor of the kidney. Am J Surg Pathol. 2004;28:1379–83.

    Article  PubMed  Google Scholar 

  38. Janssens E, Desprechins B, Ernst C, et al. Desmoplastic small round cell tumor of the kidney. JBR-BTR. 2009;92:60.

    CAS  PubMed  Google Scholar 

  39. Parvin S, Ghosh R, Das RN, et al. Primary renal rhabdomyosarcoma: an unusual bone metastasizing tumor of kidney. Fetal Pediatr Pathol. 2016;35:251–9.

    Article  PubMed  Google Scholar 

  40. Lin WC, Chen JH, Westphalen A, et al. Primary renal rhabdomyosarcoma in an adolescent with tumor thrombosis in the inferior vena cava and right atrium: a case report and review of the literature. Medicine (Baltimore). 2016;95:e3771.

    Article  Google Scholar 

  41. Kren L, Goncharuk VN, Votava M, et al. Botryoid-type of embryonal rhabdomyosarcoma of renal pelvis in an adult. A case report and review of the literature. Cesk Patol. 2003;39:31–5.

    CAS  PubMed  Google Scholar 

  42. Kaabneh A, Lang C, Eichel R, et al. Botryoid-type of embryonal rhabdomyosarcoma of renal pelvis in a young woman. Urol Ann. 2014;6:81–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Kuroda N, Inoue Y, Taguchi T, et al. Renal leiomyoma: an immunohistochemical, ultrastructural and comparative genomic hybridization study. Histol Histopathol. 2007;22:883–8.

    CAS  PubMed  Google Scholar 

  44. Lee S, Hsu H, Chang C, et al. Renal capsular leiomyoma--imaging features on computed tomography and angiography. Nephrol Dial Transplant. 2006;21:228–9.

    Article  PubMed  Google Scholar 

  45. Patil PA, Mckenney JK, Trpkov K, et al. Renal leiomyoma: a contemporary multi-institution study of an infrequent and frequently misclassified neoplasm. Am J Surg Pathol. 2015;39:349–56.

    Article  PubMed  Google Scholar 

  46. Miller JS, Zhou M, Brimo F, et al. Primary leiomyosarcoma of the kidney: a clinicopathologic study of 27 cases. Am J Surg Pathol. 2010;34:238–42.

    Article  PubMed  Google Scholar 

  47. Shah VB, Rupani AB, Deokar MS, et al. Idiopathic renal replacement lipomatosis: a case report and review of literature. Indian J Pathol Microbiol. 2009;52:552–3.

    Article  PubMed  Google Scholar 

  48. Petersson F, Michal M, Franco M, et al. Chromophobe renal cell carcinoma with liposarcomatous dedifferentiation – report of a unique case. Int J Clin Exp Pathol. 2010;3:534–40.

    PubMed  PubMed Central  Google Scholar 

  49. Anila KR, Mathew AP, Somanathan T, et al. Chromophobe renal cell carcinoma with heterologous (liposarcomatous) differentiation: a case report. Int J Surg Pathol. 2012;20:416–9.

    Article  CAS  PubMed  Google Scholar 

  50. Alvarado-Cabrero I, Folpe AL, Srigley JR, et al. Intrarenal schwannoma: a report of four cases including three cellular variants. Mod Pathol. 2000;13:851–6.

    Article  CAS  PubMed  Google Scholar 

  51. Kelley J, Collins R, Allam C. Robot-assisted laparoscopic renal schwannoma excision. J Endourol Case Rep. 2016;2:221–3.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Gobbo S, Eble JN, Huang J, et al. Schwannoma of the kidney. Mod Pathol. 2008;21:779–83.

    Article  CAS  PubMed  Google Scholar 

  53. Eble JN. Angiomyolipoma of kidney. Semin Diagn Pathol. 1998;15:21–40.

    CAS  PubMed  Google Scholar 

  54. Lin C, Jin L, Yang Y, et al. Tuberous sclerosis-associated renal angiomyolipoma: a report of two cases and review of the literature. Mol Clin Oncol. 2017;7:706–8.

    Article  PubMed  PubMed Central  Google Scholar 

  55. Nese N, Martignoni G, Fletcher CD, et al. Pure epithelioid pecomas (so-called epithelioid angiomyolipoma) of the kidney: a clinicopathologic study of 41 cases: detailed assessment of morphology and risk stratification. Am J Surg Pathol. 2011;35:161–76.

    Article  PubMed  Google Scholar 

  56. Brimo F, Robinson B, Guo C, et al. Renal epithelioid angiomyolipoma with atypia: a series of 40 cases with emphasis on clinicopathologic prognostic indicators of malignancy. Am J Surg Pathol. 2010;34:715–22.

    Article  PubMed  Google Scholar 

  57. Fine SW, Reuter VE, Epstein JI, et al. Angiomyolipoma with epithelial cysts (AMLEC): a distinct cystic variant of angiomyolipoma. Am J Surg Pathol. 2006;30:593–9.

    Article  PubMed  Google Scholar 

  58. Park BK. Renal angiomyolipoma: radiologic classification and imaging features according to the amount of fat. AJR Am J Roentgenol. 2017;209:826–35.

    Article  PubMed  Google Scholar 

  59. Jahn H, Nissen HM. Haemangioma of the urinary tract: review of the literature. Br J Urol. 1991;68:113–7.

    Article  CAS  PubMed  Google Scholar 

  60. Montgomery E, Epstein JI. Anastomosing hemangioma of the genitourinary tract: a lesion mimicking angiosarcoma. Am J Surg Pathol. 2009;33:1364–9.

    Article  PubMed  Google Scholar 

  61. Taneja K, Arora S, Rogers CG, et al. Unclassified hemangioma-like renal cell carcinoma: a potential diagnostic pitfall. Hum Pathol. 2018;75:132–6.

    Article  CAS  PubMed  Google Scholar 

  62. Ip YT, Yuan JQ, Cheung H, et al. Sporadic hemangioblastoma of the kidney: an underrecognized pseudomalignant tumor? Am J Surg Pathol. 2010;34:1695–700.

    PubMed  Google Scholar 

  63. Liu Y, Qiu XS, Wang EH. Sporadic hemangioblastoma of the kidney: a rare renal tumor. Diagn Pathol. 2012;7:49.

    Article  PubMed  PubMed Central  Google Scholar 

  64. Doyle LA, Fletcher CD. Peripheral hemangioblastoma: clinicopathologic characterization in a series of 22 cases. Am J Surg Pathol. 2014;38:119–27.

    Article  PubMed  Google Scholar 

  65. Chaabouni A, Rebai N, Fourati M, et al. Cystic lymphangioma of the kidney: diagnosis and management. Int J Surg Case Rep. 2012;3:587–9.

    Article  PubMed  PubMed Central  Google Scholar 

  66. Caduff RF, Schwobel MG, Willi UV, et al. Lymphangioma of the right kidney in an infant boy. Pediatr Pathol Lab Med. 1997;17:631–7.

    Article  CAS  PubMed  Google Scholar 

  67. Zapzalka DM, Krishnamurti L, Manivel JC, et al. Lymphangioma of the renal capsule. J Urol. 2002;168:220.

    Article  PubMed  Google Scholar 

  68. Nakai Y, Namba Y, Sugao H. Renal lymphangioma. J Urol. 1999;162:484–5.

    Article  CAS  PubMed  Google Scholar 

  69. Honma I, Takagi Y, Shigyo M, et al. Lymphangioma of the kidney. Int J Urol. 2002;9:178–82.

    Article  PubMed  Google Scholar 

  70. Topaloglu H, Karakoyunlu N, Ozok U, et al. Lymphangioma of pyeloureteral junction: an extremely rare case. Urol Int. 2013;90:243–5.

    Article  CAS  PubMed  Google Scholar 

  71. Omiyale AO. Clinicopathological features of primary angiosarcoma of the kidney: a review of 62 cases. Transl Androl Urol. 2015;4:464–73.

    PubMed  PubMed Central  Google Scholar 

  72. Brown JG, Folpe AL, Rao P, et al. Primary vascular tumors and tumor-like lesions of the kidney: a clinicopathologic analysis of 25 cases. Am J Surg Pathol. 2010;34:942–9.

    Article  PubMed  Google Scholar 

  73. Al-Ahmadie HA, Yilmaz A, Olgac S, et al. Glomus tumor of the kidney: a report of 3 cases involving renal parenchyma and review of the literature. Am J Surg Pathol. 2007;31:585–91.

    Article  PubMed  Google Scholar 

  74. Herawi M, Parwani AV, Edlow D, et al. Glomus tumor of renal pelvis: a case report and review of the literature. Hum Pathol. 2005;36:299–302.

    Article  PubMed  Google Scholar 

  75. Siddiqui N, Rogalska A, Basil IS. Glomangiomyoma (glomus tumor) of the kidney. Arch Pathol Lab Med. 2005;129:1172–4.

    PubMed  Google Scholar 

  76. Lau SK, Klein R, Jiang Z, et al. Myopericytoma of the kidney. Hum Pathol. 2010;41:1500–4.

    Article  PubMed  Google Scholar 

  77. Dhingra S, Ayala A, Chai H, et al. Renal myopericytoma: case report and review of literature. Arch Pathol Lab Med. 2012;136:563–6.

    Article  PubMed  Google Scholar 

  78. Zhang Z, Yu D, Shi H, et al. Renal myopericytoma: a case report with a literature review. Oncol Lett. 2014;7:285–7.

    Article  PubMed  Google Scholar 

  79. Lamba G, Rafiyath SM, Kaur H, et al. Malignant glomus tumor of kidney: the first reported case and review of literature. Hum Pathol. 2011;42:1200–3.

    Article  PubMed  Google Scholar 

  80. Mai K. Giant renomedullary interstitial cell tumor. J Urol. 1994;151:986–8.

    Article  CAS  PubMed  Google Scholar 

  81. Kuroda N, Toi M, Miyazaki E, et al. Participation of alpha-smooth muscle actin-positive cells in renomedullary interstitial cell tumors. Oncol Rep. 2002;9:745–50.

    CAS  PubMed  Google Scholar 

  82. Argani P, Lewin JR, Edmonds P, et al. Primary renal sclerosing epithelioid fibrosarcoma: report of 2 cases with EWSR1-CREB3L1 gene fusion. Am J Surg Pathol. 2015;39:365–73.

    Article  PubMed  PubMed Central  Google Scholar 

  83. Gelb AB, Simmons M, Weidner N. Solitary fibrous tumor involving the renal capsule. Am J Surg Pathol. 1996;20:1288–95.

    Article  CAS  PubMed  Google Scholar 

  84. Khater N, Khauli R, Shahait M, et al. Solitary fibrous tumors of the kidneys: presentation, evaluation, and treatment. Urol Int. 2013;91:373–83.

    Article  PubMed  Google Scholar 

  85. Wang J, Arber DA, Frankel K, et al. Large solitary fibrous tumor of the kidney: report of two cases and review of the literature. Am J Surg Pathol. 2001;25:1194–9.

    Article  CAS  PubMed  Google Scholar 

  86. Hasegawa T, Matsuno Y, Shimoda T, et al. Extrathoracic solitary fibrous tumors: their histological variability and potentially aggressive behavior. Hum Pathol. 1999;30:1464–73.

    Article  CAS  PubMed  Google Scholar 

  87. Doyle LA, Vivero M, Fletcher CD, et al. Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics. Mod Pathol. 2014;27:390–5.

    Article  CAS  PubMed  Google Scholar 

  88. Hasegawa T, Hirose T, Seki K, et al. Solitary fibrous tumor of the soft tissue. An immunohistochemical and ultrastructural study. Am J Clin Pathol. 1996;106:325–31.

    Article  CAS  PubMed  Google Scholar 

  89. Nishimoto K, Sumitomo M, Kakoi N, et al. Case of renal myxoma. Int J Urol. 2007;14:242–4.

    Article  PubMed  Google Scholar 

  90. Thakker P, Ramsey T, Navarro F. Renal myxoma, an incidental finding. Urol Case Rep. 2017;13:131–2.

    Article  PubMed  PubMed Central  Google Scholar 

  91. Suthar KS, Vanikar AV, Patel RD, et al. Renal myxoma- a rare variety of benign genitourinary tumour. J Clin Diagn Res. 2015;9:ED11–2.

    CAS  PubMed  PubMed Central  Google Scholar 

  92. Nielsen GP, O’connell JX, Rosenberg AE. Intramuscular myxoma: a clinicopathologic study of 51 cases with emphasis on hypercellular and hypervascular variants. Am J Surg Pathol. 1998;22:1222–7.

    Article  CAS  PubMed  Google Scholar 

  93. Wu T, Gu JQ, Duan X, et al. Hypertension due to juxtaglomerular cell tumor of the kidney. Kaohsiung J Med Sci. 2016;32:276–7.

    Article  PubMed  Google Scholar 

  94. Soni A, Gordetsky JB. Adult pleomorphic juxtaglomerular cell tumor. Urology. 2016;87:E5–7.

    Article  PubMed  Google Scholar 

  95. Kuroda N, Maris S, Monzon FA, et al. Juxtaglomerular cell tumor: a morphological, immunohistochemical and genetic study of six cases. Hum Pathol. 2013;44:47–54.

    Article  CAS  PubMed  Google Scholar 

  96. Duan X, Bruneval P, Hammadeh R, et al. Metastatic juxtaglomerular cell tumor in a 52-year-old man. Am J Surg Pathol. 2004;28:1098–102.

    Article  PubMed  Google Scholar 

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Authors and Affiliations

  1. Department of Pathology, Urology, and Oncology, Johns Hopkins Medical Institutions, Baltimore, MD, USA

    Andres Matoso

  2. Department of Pathology, Lifespan Academic Medical Center and Brown University, Providence, RI, USA

    Evgeny Yakirevich & Shamlal Mangray

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  1. Andres Matoso
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  2. Evgeny Yakirevich
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  3. Shamlal Mangray
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Correspondence to Andres Matoso .

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Editors and Affiliations

  1. Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Weill Medical College of Cornell University, Houston, TX, USA

    Mukul K. Divatia

  2. Gulhane Military Medical Academy, School of Medicine, Department of Pathology, Ankara, Turkey

    Ayhan Ozcan

  3. Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA

    Charles C. Guo

  4. Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Weill Medical College of Cornell University, Houston, TX, USA

    Jae Y. Ro

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Matoso, A., Yakirevich, E., Mangray, S. (2020). Mesenchymal Kidney Tumors. In: Divatia, M., Ozcan, A., Guo, C., Ro, J. (eds) Kidney Cancer. Springer, Cham. https://doi.org/10.1007/978-3-030-28333-9_8

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