Literature DB >> 21143835

Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case report.

Lien De Somer1, Carine Wouters, Marie-Anne Morren, Rita De Vos, Joost Van Den Oord, Koenraad Devriendt, Isabelle Meyts.   

Abstract

Rothmund-Thomson syndrome (RTS)(OMIM 268400) is a rare autosomal recessive genodermatosis characterized by poikiloderma, small stature, skeletal and dental abnormalities, cataract and an increased risk of cancer. It is caused by mutations in RECQL4 at 8q24. Immune deficiency is not described as a classical feature of the disease. Here we report the appearance of granulomatous skin lesions complicating primary Varicella Zoster Virus infection in a toddler with Rothmund Thomson syndrome and immune deficiency. Although granulomatous disorders are sometimes seen after Herpes zoster, they are even more rare after Varicella primary infection. Granulomas have hitherto not been described in Rothmund-Thomson syndrome. With this report we aim to stress the importance of screening for immune deficiency in patients with Rothmund-Thomson syndrome.

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Year:  2010        PMID: 21143835      PMCID: PMC3009952          DOI: 10.1186/1750-1172-5-37

Source DB:  PubMed          Journal:  Orphanet J Rare Dis        ISSN: 1750-1172            Impact factor:   4.123


  22 in total

1.  Successful umbilical cord blood stem cell transplantation in a patient with Rothmund-Thomson syndrome and combined immunodeficiency.

Authors:  M A Broom; L L Wang; S K Otta; A P Knutsen; E Siegfried; J R Batanian; M E Kelly; M Shah
Journal:  Clin Genet       Date:  2006-04       Impact factor: 4.438

2.  Bronchiectasis in two pediatric patients with Rothmund-Thomson syndrome.

Authors:  Philippe Reix; Jocelyne Derelle; Helene Levrey-Hadden; Henri Plauchu; Gabriel Bellon
Journal:  Pediatr Int       Date:  2007-02       Impact factor: 1.524

3.  Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene.

Authors:  L Van Maldergem; H A Siitonen; N Jalkh; E Chouery; M De Roy; V Delague; M Muenke; E W Jabs; J Cai; L L Wang; S E Plon; C Fourneau; M Kestilä; Y Gillerot; A Mégarbané; A Verloes
Journal:  J Med Genet       Date:  2005-06-17       Impact factor: 6.318

4.  IgG4 deficiency with Rothmund-Thomson syndrome: a case report.

Authors:  M Kubota; M Yasunaga; H Hashimoto; H Kimata; H Mikawa; A Shinya; C Nishigori
Journal:  Eur J Pediatr       Date:  1993-05       Impact factor: 3.183

5.  Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome.

Authors:  Lisa L Wang; Anu Gannavarapu; Claudia A Kozinetz; Moise L Levy; Richard A Lewis; Murali M Chintagumpala; Ramon Ruiz-Maldanado; Jose Contreras-Ruiz; Christopher Cunniff; Robert P Erickson; Dorit Lev; Maureen Rogers; Elaine H Zackai; Sharon E Plon
Journal:  J Natl Cancer Inst       Date:  2003-05-07       Impact factor: 13.506

Review 6.  Development of granulomatous common variable immunodeficiency subsequent to infection with Toxoplasma gondii.

Authors:  S Mrusek; A Marx; J Kummerle-Deschner; N Tzaribachev; A Enders; U-N Riede; K Warnatz; G E Dannecker; S Ehl
Journal:  Clin Exp Immunol       Date:  2004-09       Impact factor: 4.330

Review 7.  Rothmund-Thomson syndrome.

Authors:  Lidia Larizza; Gaia Roversi; Ludovica Volpi
Journal:  Orphanet J Rare Dis       Date:  2010-01-29       Impact factor: 4.123

8.  The EUROclass trial: defining subgroups in common variable immunodeficiency.

Authors:  Claudia Wehr; Teemu Kivioja; Christian Schmitt; Berne Ferry; Torsten Witte; Efrem Eren; Marcela Vlkova; Manuel Hernandez; Drahomira Detkova; Philip R Bos; Gonke Poerksen; Horst von Bernuth; Ulrich Baumann; Sigune Goldacker; Sylvia Gutenberger; Michael Schlesier; Florence Bergeron-van der Cruyssen; Magali Le Garff; Patrice Debré; Roland Jacobs; John Jones; Elizabeth Bateman; Jiri Litzman; P Martin van Hagen; Alessandro Plebani; Reinhold E Schmidt; Vojtech Thon; Isabella Quinti; Teresa Espanol; A David Webster; Helen Chapel; Mauno Vihinen; Eric Oksenhendler; Hans Hartmut Peter; Klaus Warnatz
Journal:  Blood       Date:  2007-09-26       Impact factor: 22.113

9.  Varicella-zoster virus DNA in granulomatous skin lesions following herpes zoster. A study by the polymerase chain reaction.

Authors:  U Serfling; N S Penneys; W Y Zhu; M Sisto; C Leonardi
Journal:  J Cutan Pathol       Date:  1993-02       Impact factor: 1.587

10.  Viral glycoproteins in herpesviridae granulomas.

Authors:  A F Nikkels; S Debrus; P Delvenne; C Sadzot-Delvaux; J Piette; B Rentier; G E Piérard
Journal:  Am J Dermatopathol       Date:  1994-12       Impact factor: 1.533

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  11 in total

1.  Rothmund-Thomson Syndrome-like RECQL4 truncating mutations cause a haploinsufficient low bone mass phenotype in mice.

Authors:  Wilson Castillo-Tandazo; Ann E Frazier; Natalie A Sims; Monique F Smeets; Carl R Walkley
Journal:  Mol Cell Biol       Date:  2020-12-23       Impact factor: 4.272

2.  Disseminated, persistent, and fatal infection due to the vaccine strain of varicella-zoster virus in an adult following stem cell transplantation.

Authors:  Preeti Bhalla; Graeme N Forrest; Michael Gershon; Yan Zhou; Jason Chen; Philip LaRussa; Sharon Steinberg; Anne A Gershon
Journal:  Clin Infect Dis       Date:  2014-12-01       Impact factor: 9.079

3.  The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis.

Authors:  Monique F Smeets; Elisabetta DeLuca; Meaghan Wall; Julie M Quach; Alistair M Chalk; Andrew J Deans; Jörg Heierhorst; Louise E Purton; David J Izon; Carl R Walkley
Journal:  J Clin Invest       Date:  2014-06-24       Impact factor: 14.808

4.  Immunodeficiency in a Child with Rapadilino Syndrome: A Case Report and Review of the Literature.

Authors:  M M G Vollebregt; A Malfroot; M De Raedemaecker; M van der Burg; J E van der Werff Ten Bosch
Journal:  Case Reports Immunol       Date:  2015-05-06

5.  Rothmund-Thomson syndrome and osteoma cutis in a patient previously diagnosed as COPS syndrome.

Authors:  M C van Rij; M L Grijsen; N M Appelman-Dijkstra; K B M Hansson; C A L Ruivenkamp; K Mulder; R van Doorn; A P Oranje; S G Kant
Journal:  Eur J Pediatr       Date:  2016-12-30       Impact factor: 3.183

6.  Expanding the Clinical and Genetic Spectra of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected and Unexpected Findings.

Authors:  Francesc Rudilla; Clara Franco-Jarava; Mónica Martínez-Gallo; Marina Garcia-Prat; Andrea Martín-Nalda; Jacques Rivière; Aina Aguiló-Cucurull; Laura Mongay; Francisco Vidal; Xavier Solanich; Iñaki Irastorza; Juan Luis Santos-Pérez; Jesús Tercedor Sánchez; Ivon Cuscó; Clara Serra; Noelia Baz-Redón; Mónica Fernández-Cancio; Carmen Carreras; José Manuel Vagace; Vicenç Garcia-Patos; Ricardo Pujol-Borrell; Pere Soler-Palacín; Roger Colobran
Journal:  Front Immunol       Date:  2019-10-01       Impact factor: 7.561

Review 7.  Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms.

Authors:  Megan Schmit; Anja-Katrin Bielinsky
Journal:  Int J Mol Sci       Date:  2021-01-18       Impact factor: 5.923

8.  Rothmund-Thomson Syndrome: Insights from New Patients on the Genetic Variability Underpinning Clinical Presentation and Cancer Outcome.

Authors:  Elisa A Colombo; Andrea Locatelli; Laura Cubells Sánchez; Sara Romeo; Nursel H Elcioglu; Isabelle Maystadt; Altea Esteve Martínez; Alessandra Sironi; Laura Fontana; Palma Finelli; Cristina Gervasini; Vanna Pecile; Lidia Larizza
Journal:  Int J Mol Sci       Date:  2018-04-06       Impact factor: 5.923

Review 9.  DNA Repair Syndromes and Cancer: Insights Into Genetics and Phenotype Patterns.

Authors:  Richa Sharma; Sara Lewis; Marcin W Wlodarski
Journal:  Front Pediatr       Date:  2020-10-23       Impact factor: 3.418

10.  Novel physiological RECQL4 alternative transcript disclosed by molecular characterisation of Rothmund-Thomson Syndrome sibs with mild phenotype.

Authors:  Elisa Adele Colombo; Laura Fontana; Gaia Roversi; Gloria Negri; Daniele Castiglia; Mauro Paradisi; Giovanna Zambruno; Lidia Larizza
Journal:  Eur J Hum Genet       Date:  2014-02-12       Impact factor: 4.246

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