Literature DB >> 17638432

Primary desmoplastic small round cell tumor of the kidney: a case report in a 14-year-old girl with molecular confirmation.

Sophie Collardeau-Frachon1, Dominique Ranchère-Vince, Olivier Delattre, Stelly Hoarau, Philippe Thiesse, Rémi Dubois, Christophe Bergeron, Frédérique Dijoud, Raymonde Bouvier.   

Abstract

We report a case of desmoplastic small round cell tumor (DSRCT) arising in the kidney of a 14-year-old female. The subject presented with gross hematuria. Medical imaging uncovered a left renal mass without regional or metastatic extension. The tumor showed morphological, immunohistochemical, and molecular features of DSRCT. Immunostaining revealed polyphenotypic differentiation. Molecular analysis detected the fusion transcript resulting from the t(11;22)(p13;q12) reciprocal translocation, which characterized this neoplasm. Desmoplastic small round cell tumor is a rare, aggressive neoplasm that mainly affects young males and that usually presents with widespread abdominal serosal involvement. This unusual localization should lead one to consider this tumor in the differential diagnosis of small blue round cell tumors of the kidney.

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Year:  2007        PMID: 17638432     DOI: 10.2350/06-10-0177.1

Source DB:  PubMed          Journal:  Pediatr Dev Pathol        ISSN: 1093-5266


  2 in total

Review 1.  Renal Tumors of Childhood: Radiologic-Pathologic Correlation Part 2. The 2nd Decade: From the Radiologic Pathology Archives.

Authors:  Ellen M Chung; Grant E Lattin; Kimberly E Fagen; Andrew M Kim; Michael A Pavio; Adam J Fehringer; Richard M Conran
Journal:  Radiographics       Date:  2017 Sep-Oct       Impact factor: 5.333

2.  Desmoplastic small round cell tumor of the kidney: a case report.

Authors:  Dilek Ertoy Baydar; Ayse Armutlu; Oguz Aydin; Ayhan Dagdemir; Yarkin Kamil Yakupoglu
Journal:  Diagn Pathol       Date:  2020-07-23       Impact factor: 2.644

  2 in total

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