Literature DB >> 21337690

Angiosarcoma in a patient with immunodeficiency, centromeric region instability, facial anomalies (ICF) syndrome.

Michiel van den Brand1, Uta E Flucke, Peter Bult, Corry M R Weemaes, Marcel van Deuren.   

Abstract

The Immunodeficiency, Centromeric region instability, and Facial anomalies (ICF) syndrome (OMIM #242860) is a rare autosomal recessive disorder caused by defective DNA methylation. Hematological disease and malignancy (macrophage activation syndrome, myelodysplastic syndrome, and Hodgkin lymphoma) have been reported in three patients. To date, there have been no reports of either epithelial or mesenchymal malignancies. We present a patient with all clinical and laboratory findings of the ICF syndrome who died of a metastatic angiosarcoma of the liver. This is the first report of a non-hematological malignancy in the ICF syndrome. The young age at which our patient developed an angiosarcoma suggests an effect of the defective DNA methylation observed in the ICF syndrome. Therefore, with improvement of recognition and treatment of the ICF syndrome, malignancy could become more common in this condition.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21337690     DOI: 10.1002/ajmg.a.33831

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  5 in total

1.  Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey.

Authors:  Delphine Sterlin; Guillaume Velasco; Despina Moshous; Fabien Touzot; Nizar Mahlaoui; Alain Fischer; Felipe Suarez; Claire Francastel; Capucine Picard
Journal:  J Clin Immunol       Date:  2016-02-06       Impact factor: 8.317

2.  Immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome, due to ZBTB24 mutations, presenting with large cerebral cyst.

Authors:  Manuela Cerbone; Jun Wang; Silvère M Van der Maarel; Alessandra D'Amico; Antonio D'Agostino; Alfonso Romano; Nicola Brunetti-Pierri
Journal:  Am J Med Genet A       Date:  2012-07-11       Impact factor: 2.802

3.  Liver failure due to hepatic angiosarcoma in an adolescent with dyskeratosis congenita.

Authors:  Timothy S Olson; Elaine S Chan; Michele E Paessler; Kathleen E Sullivan; Christopher N Frantz; Piere Russo; Monica Bessler
Journal:  J Pediatr Hematol Oncol       Date:  2014-05       Impact factor: 1.289

4.  Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects.

Authors:  Corry M R Weemaes; Maarten J D van Tol; Jun Wang; Monique M van Ostaijen-ten Dam; Marja C J A van Eggermond; Peter E Thijssen; Caner Aytekin; Nicola Brunetti-Pierri; Mirjam van der Burg; E Graham Davies; Alina Ferster; Dieter Furthner; Giorgio Gimelli; Andy Gennery; Barbara Kloeckener-Gruissem; Stephan Meyn; Cynthia Powell; Ismail Reisli; Catharina Schuetz; Ansgar Schulz; Andrea Shugar; Peter J van den Elsen; Silvère M van der Maarel
Journal:  Eur J Hum Genet       Date:  2013-03-13       Impact factor: 4.246

Review 5.  Dnmt3b Prefers Germ Line Genes and Centromeric Regions: Lessons from the ICF Syndrome and Cancer and Implications for Diseases.

Authors:  Emma L Walton; Claire Francastel; Guillaume Velasco
Journal:  Biology (Basel)       Date:  2014-09-05
  5 in total

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