Literature DB >> 18452823

Familial papillary renal carcinoma: cytogenetic characterization in normal and tumor tissues in two brothers. A case report.

Michele Gallucci1, Erika Vico, Steno Sentinelli, Costantino Leonardo, Paulo Visca, Giulia Orlandi, AnnaMaria Cianciulli.   

Abstract

BACKGROUND: Renal tumor subtypes are associated with distinct, recurring cytogenetic abnormalities and hereditary cancer syndromes. In papillary renal carcinoma, trisomy 7 and 17 and loss of the Y chromosome are the most common chromosomal defects. CASE
PRESENTATION: The present paper analyzes the chromosomes 7, 17, and Y alterations found in familial papillary carcinoma and in the normal tissue of two brothers. The evaluation, performed by fluorescence in situ hybridization (FISH) and cytogenetic conventional methods, was carried out on blood samples, normal kidney tissue, and tumor samples of the two brothers. Patient 1 showed gains of chromosomes 7 and 17 both in normal and tumor tissue. Chromosome Y status was normal. Patient 2 showed chromosome 7 and 17 gains, chromosome Y loss in tumor and chromosome 17 and Y alterations in normal kidney tissue. The constitutional karyotype was normal in both brothers.
CONCLUSIONS: Of particular relevance were the chromosome aberrations found in normal kidney parenchyma. In fact, the progressive alterations of 7, 17, and Y chromosomes could provide evidence of early genetic instability of tissue and may even precede the development of macroscopically identifiable lesions.

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Year:  2008        PMID: 18452823     DOI: 10.1016/j.urolonc.2007.01.025

Source DB:  PubMed          Journal:  Urol Oncol        ISSN: 1078-1439            Impact factor:   3.498


  1 in total

1.  Ewing's sarcoma of the kidney.

Authors:  Joel R Angel; Anushayanthan Alfred; Ankit Sakhuja; Ryan E Sells; Joseph John Zechlinski
Journal:  Int J Clin Oncol       Date:  2010-03-04       Impact factor: 3.402

  1 in total

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