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Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia

Schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphyseal dysplasia. Mutations in SWI/SNF2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1...

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Autores principales: Basiratnia, Mitra, Baradaran-Heravi, Alireza, Yavarian, Majid, Geramizadeh, Bita, Karimi, Mehran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University of Medical Sciences 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556764/
https://www.ncbi.nlm.nih.gov/pubmed/23359635
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author Basiratnia, Mitra
Baradaran-Heravi, Alireza
Yavarian, Majid
Geramizadeh, Bita
Karimi, Mehran
author_facet Basiratnia, Mitra
Baradaran-Heravi, Alireza
Yavarian, Majid
Geramizadeh, Bita
Karimi, Mehran
author_sort Basiratnia, Mitra
collection PubMed
description Schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphyseal dysplasia. Mutations in SWI/SNF2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 (SMARCAL1) gene are responsible for the disease. The present report describes, for the first time, a Schimke immuno-osseous dysplasia child with SMARCAL1 missense mutation (R561H) and manifestations of intussusception secondary to Epstein-Barr virus-negative non-Hodgkin lymphoma, who expired due to septicemia following chemotherapy. The report emphasizes the necessity of more limited immunosuppressive protocols in Schimke immuno-osseous dysplasia patients with lymphoproliferative disorders.
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spelling pubmed-35567642013-01-28 Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia Basiratnia, Mitra Baradaran-Heravi, Alireza Yavarian, Majid Geramizadeh, Bita Karimi, Mehran Iran J Med Sci Case Schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphyseal dysplasia. Mutations in SWI/SNF2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 (SMARCAL1) gene are responsible for the disease. The present report describes, for the first time, a Schimke immuno-osseous dysplasia child with SMARCAL1 missense mutation (R561H) and manifestations of intussusception secondary to Epstein-Barr virus-negative non-Hodgkin lymphoma, who expired due to septicemia following chemotherapy. The report emphasizes the necessity of more limited immunosuppressive protocols in Schimke immuno-osseous dysplasia patients with lymphoproliferative disorders. Shiraz University of Medical Sciences 2011-09 /pmc/articles/PMC3556764/ /pubmed/23359635 Text en © 2011: Iranian Journal of Medical Sciences
spellingShingle Case
Basiratnia, Mitra
Baradaran-Heravi, Alireza
Yavarian, Majid
Geramizadeh, Bita
Karimi, Mehran
Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia
title Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia
title_full Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia
title_fullStr Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia
title_full_unstemmed Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia
title_short Non-Hodgkin Lymphoma in a Child with Schimke Immuno-Osseous Dysplasia
title_sort non-hodgkin lymphoma in a child with schimke immuno-osseous dysplasia
topic Case
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556764/
https://www.ncbi.nlm.nih.gov/pubmed/23359635
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