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Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings
Autoimmune polyglandular syndrome type 1 (APS1) is a rare autosomal recessive disorder, and large granular lymphocytic leukemia (LGLL) may, even more rarely, complicate APS1. LGLL may be subtle in presentation, but it is imperative to recognize LGLL in APS1 promptly, as outcome may otherwise be fata...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930195/ https://www.ncbi.nlm.nih.gov/pubmed/29744070 http://dx.doi.org/10.1002/ccr3.1454 |
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author | Harrison, Jonathan S. Parmar, Harsh Wang, Xiangbing D. |
author_facet | Harrison, Jonathan S. Parmar, Harsh Wang, Xiangbing D. |
author_sort | Harrison, Jonathan S. |
collection | PubMed |
description | Autoimmune polyglandular syndrome type 1 (APS1) is a rare autosomal recessive disorder, and large granular lymphocytic leukemia (LGLL) may, even more rarely, complicate APS1. LGLL may be subtle in presentation, but it is imperative to recognize LGLL in APS1 promptly, as outcome may otherwise be fatal, as described herein. |
format | Online Article Text |
id | pubmed-5930195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59301952018-05-09 Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings Harrison, Jonathan S. Parmar, Harsh Wang, Xiangbing D. Clin Case Rep Case Reports Autoimmune polyglandular syndrome type 1 (APS1) is a rare autosomal recessive disorder, and large granular lymphocytic leukemia (LGLL) may, even more rarely, complicate APS1. LGLL may be subtle in presentation, but it is imperative to recognize LGLL in APS1 promptly, as outcome may otherwise be fatal, as described herein. John Wiley and Sons Inc. 2018-03-11 /pmc/articles/PMC5930195/ /pubmed/29744070 http://dx.doi.org/10.1002/ccr3.1454 Text en © 2018 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Harrison, Jonathan S. Parmar, Harsh Wang, Xiangbing D. Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings |
title | Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings |
title_full | Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings |
title_fullStr | Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings |
title_full_unstemmed | Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings |
title_short | Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings |
title_sort | large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930195/ https://www.ncbi.nlm.nih.gov/pubmed/29744070 http://dx.doi.org/10.1002/ccr3.1454 |
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