Human Pathology
Volume 41, Issue 10 , Pages 1495-1499, October 2010

Anaplastic sarcoma of the kidney with chromosomal abnormality: first report on cytogenetic findings

  • Kiyoshi Gomi, MD, PhD

      Affiliations

    • Division of Pathology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
    • Corresponding Author InformationCorresponding author. Division of Pathology, Kanagawa Children's Medical Center, Yokohama City, Kanagawa Prefecture, 232-8555, Japan.
  • ,
  • Satoshi Hamanoue, MD, PhD

      Affiliations

    • Division of Hemato-oncology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
  • ,
  • Mio Tanaka, MD, PhD

      Affiliations

    • Division of Pathology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
  • ,
  • Masae Matsumoto, MD, PhD

      Affiliations

    • Division of Hemato-oncology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
  • ,
  • Norihiko Kitagawa, MD, PhD

      Affiliations

    • Division of Surgery, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
  • ,
  • Tetsu Niwa, MD, PhD

      Affiliations

    • Division of Radiology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
  • ,
  • Noriko Aida, MD, PhD

      Affiliations

    • Division of Radiology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
  • ,
  • Hisato Kigasawa, MD, PhD

      Affiliations

    • Division of Hemato-oncology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan
  • ,
  • Yukichi Tanaka, MD, PhD

      Affiliations

    • Division of Pathology, Kanagawa Children's Medical Center, Yokohama, 232-8555 Japan

Received 6 January 2010; received in revised form 22 February 2010; accepted 11 March 2010. published online 26 July 2010.

Summary 

We report a case of anaplastic sarcoma of the kidney (ASK) with cytogenetic findings. A 12-year-old Japanese girl presented with buttock pain and urinary incontinence. Radiological investigations revealed a right renal tumor with multiple distant metastases and multicystic thyroid tumor. She underwent radical right nephrectomy and subsequently received chemotherapy and radiation therapy. Histologically, the renal tumor demonstrated admixture of various types of mesenchymal elements: cellular spindle cells with anaplastic features, cartilage, and rhabdomyoblastic cells consistent with ASK. Chromosomal analysis revealed the karyotype of the tumor cells to be 46, XX, +8, –10, der (18) t (10; 18) (q21; p11.2). The thyroid tumor was removed later and diagnosed as adenomatous goiter. To our knowledge, this is the first case of ASK with chromosomal abnormality and may provide new insight into the molecular biologic basis of this rare renal tumor.

Keywords: Anaplastic sarcoma of kidney, Renal tumor, Children, Chromosomal abnormality

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PII: S0046-8177(10)00133-4

doi:10.1016/j.humpath.2010.03.008

Human Pathology
Volume 41, Issue 10 , Pages 1495-1499, October 2010