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Clear cell sarcoma of the kidney in children: experience in a developing country

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Abstract

Introduction

Clear cell sarcoma of the kidney (CCSK) is a rare tumour comprising 4% of primary renal tumours in children. It has a unique constellation of chromosomal and molecular features and should no longer be viewed as an unfavourable histological variant of Wilms tumour. Little is known of its clinical presentation and pathological profile in children living in a developing country.

Aim

To describe the clinical and pathological features of CCSK in children in our practice and to identify factors contributing to poor patient outcomes.

Method

A retrospective review of patients with a confirmed diagnosis of CCSK who presented for treatment at a single institution between 1990 and 2008.

Results

14 patients fulfilled the inception criteria. They represented 4% of 356 patients presenting with primary renal tumours during the review period. Clinical and radiological features were indistinguishable from Wilms tumour. Tumours were large (Mean mass 1.4 kg; median 0.9 kg) and metastases were common (42%). Lung and lymph node metastases were more common than skeletal disease. Co-morbidity, particularly hypertension (64%) was common. Initial diagnosis by needle biopsy was correct in only two of seven patients (29%) leading to inappropriate neoadjuvant chemotherapy. Overall survival is poor with 57% of patients alive and disease free from 1 to 7 years off treatment.

Conclusion

In a developing country, CCSK is rare and clinically and radiologically indistinguishable from Wilms tumour. Associated hypertension is common. Pretreatment diagnosis is difficult and sampling errors using needle biopsies may be unavoidable. Treatment results are poor and, given the propensity for late recurrence in CCSK, may not be sustained.

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References

  1. Kidd JM (1970) Exclusion of certain renal neoplasms from the category of Wilms tumor (abstract) American. J Pathol 59:16a

    Google Scholar 

  2. Morgan E, Kidd JM (1978) Undifferentiated sarcoma of the kidney: a tumor with histopathologic and clinical characteristics distinct from Wilms tumor. Cancer 42(4):1916–1921

    Article  CAS  PubMed  Google Scholar 

  3. Yun K (1993) Clear cell sarcoma of the kidney expresses insulin like growth factor-ll but not WT1 transcripts. Am J Pathol 142(1):39–47

    CAS  PubMed  Google Scholar 

  4. Jones C, Rodriguez-Pinilla M, Lambros M, Bax D, Messahel B, Vujanic GM, Reis-Filho JS, Pritchard-Jones K (2007) c-KIT overexpression, without gene amplification and mutation, in paediatric renal tumours. J Clin Pathol 60(11):1226–1231

    Article  CAS  PubMed  Google Scholar 

  5. Little SE, Bax DA, Rodriguez-Pinilla M, Natrajan R, Messahel B, Pritchard-Jones K, Vujanic GM, Reis-Filho JS, Jones C (2007) Multifaceted dysregulation of the epidermal growth factor receptor pathway in clear cell sarcoma of the kidney. Clin Cancer Res 13(15 Pt 1):4360–4364

    Article  CAS  PubMed  Google Scholar 

  6. Brownlee NA, Perkins LA, Stewart W, Jackle B, Pettenati MJ, Koty PP, Iskandar SS, Garvin AJ (2007) Recurring translocation (10;17) and deletion (14q) in clear cell sarcoma of the kidney. Arch Pathol Lab Med 131(3):446–451

    PubMed  Google Scholar 

  7. Cutcliffe C, Kersey D, Huang CC, Zeng Y, Walterhouse D, Perlman EJ (2005) Renal Tumor Committee of the Children’s Oncology Group. Clear cell sarcoma of the kidney: up-regulation of neural markers with activation of the sonic hedgehog and Akt pathways. Clin Cancer Res 11(22):7986–7994

    Article  CAS  PubMed  Google Scholar 

  8. Rakheja D, Weinberg AG, Tomlinson GE, Partridge K, Schneider NR (2004) Translocation (10;17)(q22;p13): a recurring translocation in clear cell sarcoma of kidney. Cancer Genet Cytogenet 154(2):175–179

    Article  CAS  PubMed  Google Scholar 

  9. Pastore G, Znaor A, Spreafico F, Graf N, Pritchard-Jones K, Steliarova-Foucher E (2006) Malignant renal tumours incidence and survival in European children (1978–1997): report from the Automated Childhood Cancer Information System project. Eur J Cancer 42(13):2103–2114

    Article  PubMed  Google Scholar 

  10. Argani P, Perlman EJ, Breslow NE, Browning NG, Green DM, D’Angio GJ, Beckwith JB (2000) Clear cell sarcoma of the kidney: a review of 351 cases from the National Wilms Tumor Study Group Pathology Center. Am J Surg Pathol 24(1):4–18

    Article  CAS  PubMed  Google Scholar 

  11. Ahmed HU, Arya M, Levitt G, Duffy P, Sebire N, Mushtaq I (2007) Part ll: Treatment of primary non-Wilms’ renal tumours in children. Lancet Oncol 8(9):730–737

    Article  PubMed  Google Scholar 

  12. Zigman A, Shen I (2006) Clear cell sarcoma of the kidney with cavo-atrial tumor thrombus: complete resection in a child. J Pediatr Surg 41(8):1464–1466

    Article  PubMed  Google Scholar 

  13. Feusner JH, Beckwith JB, D’Angio GJ (1990) Clear cell sarcoma of the kidney: accuracy of imaging methods for detecting bone metastases. Report from the National Wilms’ Tumor Study. Med Pediatr Oncol 18(3):225–227

    Article  CAS  PubMed  Google Scholar 

  14. Kural AR, Onal B, Ozkara H, Cakarir C, Ayan I, Agaoglu FY (2006) Adult clear cell sarcoma of the kidney: a case report. BMC Urol 6:11

    Article  PubMed  Google Scholar 

  15. Oue T, Fukuzawa M, Okita H, Mugishima H et al (2009) Outcme of pedaitric renal tumour treated using the Japan Wilms Tumor Study-1 (JWiTS-1) protocol: a report from the JWiTS Group. Pediatr Surg Int 25(11):923–929

    Article  PubMed  Google Scholar 

  16. Green DM, Breslow NE, Beckwith JB, Moksness J, Finklestein JZ, D’Angio GJ (1994) Treatment of children with clear-cell sarcoma of the kidney: a report from the National Wilms’ Tumor Study Group. J Clin Oncol 12(10):2132–2137

    CAS  PubMed  Google Scholar 

  17. Seibel NL, Li S, Breslow NE, Beckwith JB, Green DM, Haase GM, Ritchey ML, Thomas PR, Grundy PE, Finklestein JZ, Kim T, Shochat SJ, Kelalis PP, D’Angio GJ (2004) Effect of duration of treatment on treatment outcome for patients with clear-cell sarcoma of the kidney: a report from the National Wilms’ Tumor Study Group. J Clin Oncol 22(3):468–473

    Article  PubMed  Google Scholar 

  18. Miniati D, Gay AN, Parks KV, Naik-Mathuria BJ, Hicks J, Nuchtern JG, Cass DL, Olutoye OO (2008) Imaging accuracy and incidence of Wilms’ and non-Wilms’ renal tumors in children. J Pediatr Surg 43(7):1301–1307

    Article  PubMed  Google Scholar 

  19. Portugal R, Barroca H (2008) Clear cell sarcoma, cellular mesoblastic nephroma and metanephric adenoma: cytological features and differential diagnosis from Wilms tumour. Cytopathology 19(2):80–85

    Article  CAS  PubMed  Google Scholar 

  20. Iyer VK, Agarwala S, Verma K (2005) Fine-needle aspiration cytology of clear-cell sarcoma of the kidney: study of eight cases. Diagn Cytopathol 33(2):83–89

    Article  PubMed  Google Scholar 

  21. Balarezo FS, Joshi VV (2001) CCSK of the paediatric kidney:detailed description and analysis of variant histologic patterns of a tumor with many faces. Adv Anat Pathol 8:98–108

    Article  CAS  PubMed  Google Scholar 

  22. Murphy WM, Grignon DJ, Perlman EJ (eds) (2004) Tumours of the kidney, bladder and related structures. Armed forced Institute of Pathology, Washington DC, pp 1–100

  23. Pritchard-Jones K, Fleming S (1991) Cell types expressing Wilms’ tumour gene WT1 in Wilms’ tumours implications for tumour histogenesis. Oncogene 6:2211–2220

    CAS  PubMed  Google Scholar 

  24. Ahmed HU, Arya M, Levitt G, Duffy P, Mushtaq I, Sebire N (2007) Part l: Primary non-Wilms’ tumours in children. Lancet Oncol 8(8):730–737

    Article  PubMed  Google Scholar 

  25. Kusumakumary P, Chellam VG, Rojymon J, Hariharan S, Krishnan NM (1997) Late recurrence of clear cell sarcoma of the kidney. Med Pediatr Oncol 28(5):355–357

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

The contribution of Dr Yetish Sing FCPath(SA) of the Department of Anatomical Pathology at Inkosi Albert Luthuli Hospital to our understanding of the pathology of CCSK is gratefully acknowledged

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Correspondence to G. P. Hadley.

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Hadley, G.P., Sheik-Gafoor, M.H. Clear cell sarcoma of the kidney in children: experience in a developing country. Pediatr Surg Int 26, 345–348 (2010). https://doi.org/10.1007/s00383-010-2554-0

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