期刊论文详细信息
BMC Research Notes
Clear cell sarcoma of the kidney distinguished from synovial sarcoma using genetic analysis: a case report
Yutaro Hayashi1  Kenjiro Kohri1  Yoshinobu Moritoki1  Hidenori Nishio1  Hideyuki Kamisawa1  Kentaro Mizuno1  Masahito Hirose1 
[1] Department of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Aichi, Japan
关键词: Pediatric renal tumor;    Sarcoma;    Gene analysis;   
Others  :  1164299
DOI  :  10.1186/s13104-015-1100-5
 received in 2015-03-08, accepted in 2015-03-26,  发布年份 2015
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【 摘 要 】

Background

The most common pediatric renal neoplasm is Wilms tumor, but clear cell sarcoma of the kidney or synovial sarcoma of the kidney are also sometimes encountered. Accurate pathological diagnosis is important, because adjuvant therapies including chemotherapy and radiotherapy differ according to the pathological type.

Case presentation

A 9-year-old boy presented with a headache, and ultrasonography, computed tomography, and magnetic resonance imaging revealed a heterogeneous enhancement of soft tissue originating from the upper pole of the left kidney, measuring approximately 11.0 × 10.0 × 8.0 cm. A left radical nephrectomy was performed using an intraperitoneal approach through an anterior subcostal incision. Pathological examination suggested clear cell sarcoma of the kidney or synovial sarcoma of the kidney based on morphological and immunohistological features. Using genetic analysis, a final diagnosis of spindle cell pattern clear cell sarcoma of the kidney was made based on the absence of the SYT-SSX fusion gene. After adjuvant chemo-radiotherapy was administered, no recurrence or metastasis has been identified as of 60 months postoperatively.

Conclusion

In this case, it was difficult to discriminate clear cell sarcoma of the kidney from synovial sarcoma of the kidney based on histopathological examination alone, and genetic analysis was required. Accurate pathological diagnosis of pediatric renal tumor is important for determining optimal treatment and preventing recurrence and metastasis.

【 授权许可】

   
2015 Hirose et al.; licensee BioMed Central.

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【 参考文献 】
  • [1]Kidd JM: Exclusion of certain renal neoplasms from the category of Wilms’ tumor. Am J Pathol 1970, 59:16a.
  • [2]Argani P, Faria PA, Epstein JI, Reuter VE, Perlman EJ, Beckwith JB, 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.
  • [3]Beckwith JB: National Wilms tumor study: an update for pathologists. Pediatr Dev Pathol 1998, 1:79-84.
  • [4]Oue T, Fukuzawa M, Okita H, Mugishima H, Horie H, Hata J, et al.: Outcome of pediatric renal tumor treated using the Japan Wilms Tumor Study-1 (JWiTS-1) protocol: a report from the JWiTS group. Pediatr Surg Int 2009, 25:923-9.
  • [5]Argani P, Perlman EJ, Breslow NE, Browning NG, Green DM, D’Angio GJ, et al.: Clear cell sarcoma of the kidney: a review of 351 cases from the National Wilms Tumor Study Group Pathology Center. Am J Surg Pathol 2000, 24:4-18.
  • [6]Ahmed HU, Arya M, Levitt G, Duffy PG, Mushtaq I, Part SNJ: Primary malignant non-Wilms’ renal tumours in children. Lancet Oncol 2007, 8:730-7.
  • [7]Kim DH, Sohn JH, Lee MC, Lee G, Yoon GS, Hashimoto H, et al.: Primary synovial sarcoma of the kidney. Am J Surg Pathol 2000, 24:1097-104.
  • [8]Perlmutter AE, Saunders SE, Zaslau S, Chang WW, Farivar-Mohseni H: Primary synovial sarcoma of the kidney. Int J Urol 2005, 12:760-2.
  • [9]Chung SD, Huang KH, Chueh SC, Lai MK, Lin WC: Primary synovial sarcoma of the kidney. J Formos Med Assoc 2008, 107:344-7.
  • [10]Rekhi B, Basak R, Desai SB, Jambhekar NA: Immunohistochemical validation of TLE1, a novel marker, for synovial sarcomas. Indian J Med Res 2012, 136:766-75.
  • [11]Dai YC, Wu HM, Chang CW, Liou CP, Tzeng CC: A rare synovial sarcoma of the kidney exhibiting translocation (X;18) and SYT-SSX2 fusion gene. Zhonghua Yi Xue Za Zhi (Taipei) 2002, 65:293-7.
  • [12]Nishio J, Iwasaki H, Ishiguro M, Ohjimi Y, Isayama T, Naito M, et al.: Synovial sarcoma with a secondary chromosome change der(22)t(17;22)(q12;q12). Cancer Genet Cytogenet 2002, 137:23-8.
  • [13]O’Meara E, Stack D, Lee CH, Garvin AJ, Morris T, Argani P, et al.: Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney. J Pathol 2012, 227:72-80.
  • [14]Benchekroun A, Zannoud M, el Alj HA, Nouini Y, Marzouk M, Faik M: Clear cell sarcoma of the kidney: 3 case reports. Prog Urol 2002, 12:469-73.
  • [15]Bhayani SB, Liapis H, Kibel AS: Adult clear cell sarcoma of the kidney with atrial tumor thrombus. J Urol 2001, 165:896-7.
  • [16]Ahmed HU, Arya M, Levitt G, Duffy PG, Sebire NJ, Part MI, et al.: Treatment of primary malignant non-Wilms’ renal tumours in children. Lancet Oncol 2007, 8:842-8.
  • [17]Kampe CE, Rosen G, Eilber F, Eckardt J, Lowenbraun S, Foster J, et al.: Synovial sarcoma. A study of intensive chemotherapy in 14 patients with localized disease. Cancer 1993, 72:2161-9.
  • [18]Bella AJ, Winquist EW, Perlman EJ: Primary synovial sarcoma of the kidney diagnosed by molecular detection of SYT-SSX fusion transcripts. J Urol 2002, 168:1092-3.
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