Literature DB >> 15069403

HHV-8-associated Kaposi sarcoma in a child with IFNgammaR1 deficiency.

Yildiz Camcioglu1, Capucine Picard, Vincent Lacoste, Stéphanie Dupuis, Necla Akçakaya, Haluk Cokura, Gültekin Kaner, Cuyan Demirkesen, Sabine Plancoulaine, Jean-François Emile, Antoine Gessain, Jean-Laurent Casanova.   

Abstract

OBJECTIVES: Mediterranean classic Kaposi sarcoma (KS) of childhood is rare and unexplained. Our objective is to describe the case of a child with complete IFNgammaR1 deficiency and severe mycobacterial disease in whom Kaposi sarcoma (KS) developed.
RESULTS: Disseminated mycobacterial infection began at the age of 5 months, and at 11 years of age the child had disseminated KS lesions. The histologic appearance of these lesions was typical, with endothelial and spindle cell proliferation. Human herpesvirus-8 (HHV-8)-associated antigens were detected in situ by immunohistochemistry. HHV-8 DNA of K1 molecular subtype A was amplified from tissue lesions, and HHV-8-specific antibodies were detected in the patient's serum. The child died at 12 years of age of disseminated mycobacterial disease and KS.
CONCLUSIONS: This is the first identification of a well-defined primary immunodeficiency in a child with KS. Inherited disorders of IFN-gamma-mediated immunity and severe mycobacterial disease may predispose HHV-8-infected children to KS.

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Year:  2004        PMID: 15069403     DOI: 10.1016/j.jpeds.2003.11.012

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  42 in total

1.  Disseminated Mycobacterium Avium Infection in a Child with Complete Interferon-γ Receptor 1 Deficiency due to Compound Heterozygosis of IFNGR1 for a Subpolymorphic Copy Number Variation and a Novel Splice-Site Variant.

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Journal:  J Pediatr Genet       Date:  2019-11-04

Review 2.  Immunity to microbes: lessons from primary immunodeficiencies.

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Journal:  Infect Immun       Date:  2007-02-05       Impact factor: 3.441

Review 3.  Diagnostic and therapeutic challenges in a child with complete interferon-γ receptor 1 deficiency.

Authors:  Peter Olbrich; Maria Teresa Martínez-Saavedra; José Maria Perez-Hurtado; Cristina Sanchez; Berta Sanchez; Caroline Deswarte; Ignacio Obando; Jean-Laurent Casanova; Carsten Speckmann; Jacinta Bustamante; Carlos Rodriguez-Gallego; Olaf Neth
Journal:  Pediatr Blood Cancer       Date:  2015-07-14       Impact factor: 3.167

4.  Clinical and host genetic characteristics of Mendelian susceptibility to mycobacterial diseases in Japan.

Authors:  Takayuki Hoshina; Hidetoshi Takada; Yuka Sasaki-Mihara; Koichi Kusuhara; Koichi Ohshima; Satoshi Okada; Masao Kobayashi; Osamu Ohara; Toshiro Hara
Journal:  J Clin Immunol       Date:  2011-01-08       Impact factor: 8.317

5.  B-cell lymphoma in a patient with complete interferon gamma receptor 1 deficiency.

Authors:  Hannelore I Bax; Alexandra F Freeman; Victoria L Anderson; Per Vesterhus; Dan Laerum; Stefania Pittaluga; Wyndham H Wilson; Steven M Holland
Journal:  J Clin Immunol       Date:  2013-06-26       Impact factor: 8.317

Review 6.  Human inborn errors of immunity to herpes viruses.

Authors:  Emmanuelle Jouanguy; Vivien Béziat; Trine H Mogensen; Jean-Laurent Casanova; Stuart G Tangye; Shen-Ying Zhang
Journal:  Curr Opin Immunol       Date:  2020-01-31       Impact factor: 7.486

7.  Interleukin 1 receptor-associated kinase 1 (IRAK1) mutation is a common, essential driver for Kaposi sarcoma herpesvirus lymphoma.

Authors:  Dongmei Yang; Wuguo Chen; Jie Xiong; Carly J Sherrod; David H Henry; Dirk P Dittmer
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-23       Impact factor: 11.205

8.  Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion.

Authors:  Carolyn C Jackson; Alain Lefèvre-Utile; Anne Guimier; Valérie Malan; Julie Bruneau; Antoine Gessain; Olivier Cassar; Jeanne Amiel; Aurélie Cobat; Vimel Rattina; Laurent Abel; Jean-Laurent Casanova; Stéphane Blanche
Journal:  Am J Med Genet A       Date:  2017-05-09       Impact factor: 2.802

Review 9.  Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity.

Authors:  Jacinta Bustamante; Stéphanie Boisson-Dupuis; Laurent Abel; Jean-Laurent Casanova
Journal:  Semin Immunol       Date:  2014-10-26       Impact factor: 11.130

Review 10.  Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiency.

Authors:  Carolina Prando; Stéphanie Boisson-Dupuis; Audrey V Grant; Xiao-Fei Kong; Jacinta Bustamante; Jacqueline Feinberg; Ariane Chapgier; Yoann Rose; Lucile Jannière; Elena Rizzardi; Qiuping Zhang; Catherine M Shanahan; Louis Viollet; Stanislas Lyonnet; Laurent Abel; Ezia Maria Ruga; Jean-Laurent Casanova
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

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