Literature DB >> 10466454

Mesoblastic nephroma in adulthood: a case report.

K Shiraishi1, M Yamamoto, T Gondo, S Shirataki, K Naito.   

Abstract

BACKGROUND: Mesoblastic nephroma is an uncommon renal tumor of infancy and rarely occurs in adults. We report an adult case of mesoblastic nephroma.
METHODS: A 50-year-old woman was found incidentally to have a right renal mass by abdominal ultrasonography. Computed tomography and magnetic resonance imaging revealed a heterogeneous tumor and angiography showed a mixture of hypervascularity and hypovascularity. Right radical nephrectomy was performed.
RESULTS: The tumor was an encapsulated yellowish solid mass. Microscopically, the tumor was composed of spindle cell proliferation. Atypia and mitoses were not identified. Among the tumor cells, there were tubular arranged epithelial elements.
CONCLUSION: The patient was free of recurrence 14 months postoperatively. Mesoblastic nephroma is classified as a benign tumor but recurrence and malignant formation of this tumor have been reported so regular postoperative follow up is required.

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Year:  1999        PMID: 10466454     DOI: 10.1046/j.1442-2042.1999.00085.x

Source DB:  PubMed          Journal:  Int J Urol        ISSN: 0919-8172            Impact factor:   3.369


  1 in total

1.  Multiphasic contrast-enhanced CT and MRI findings of adult mesoblastic nephroma: A report of two cases.

Authors:  Yuqin Ding; Deming He; Jianjun Zhou; Mengsu Zeng
Journal:  Indian J Radiol Imaging       Date:  2013-01
  1 in total

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