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Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report
Severe chronic neutropenia is classified as severe congenital, cyclic, autoimmune, or idiopathic. However, there is a lot of uncertainty regarding the diagnosis of severe congenital neutropenia (SCN) and chronic idiopathic neutropenia, and this uncertainty affects further evaluations and treatments....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Journal of Yeungnam Medical Science
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390272/ https://www.ncbi.nlm.nih.gov/pubmed/35899327 http://dx.doi.org/10.12701/jyms.2022.00353 |
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author | Kim, Juhyung Hwang, Soyoon Hwang, Narae Lee, Yeonji Cho, Hee Jeong Moon, Joon Ho Sohn, Sang Kyun Baek, Dong Won |
author_facet | Kim, Juhyung Hwang, Soyoon Hwang, Narae Lee, Yeonji Cho, Hee Jeong Moon, Joon Ho Sohn, Sang Kyun Baek, Dong Won |
author_sort | Kim, Juhyung |
collection | PubMed |
description | Severe chronic neutropenia is classified as severe congenital, cyclic, autoimmune, or idiopathic. However, there is a lot of uncertainty regarding the diagnosis of severe congenital neutropenia (SCN) and chronic idiopathic neutropenia, and this uncertainty affects further evaluations and treatments. A 20-year-old man presented with fever and knee abrasions after a bicycle accident. On admission, his initial absolute neutrophil count (ANC) was 30/µL. He had no medical history of persistent severe neutropenia with periodic oscillation of ANC. Although his fever resolved after appropriate antibiotic therapy, ANC remained at 80/µL. Bone marrow (BM) aspiration and biopsy were performed, and a BM smear showed myeloid maturation arrest. Moreover, genetic mutation test results showed a heterozygous missense variant in exon 4 of the neutrophil elastase ELANE: c597+1G>C (pV190-F199del). The patient was diagnosed with SCN. After discharge, we routinely checked his ANC level and monitored any signs of infection with minimum use of granulocyte colony-stimulating factor (G-CSF), considering its potential risk of leukemic transformation. Considering that SCN can be fatal, timely diagnosis and appropriate management with G-CSF are essential. We report the case of a patient with SCN caused by ELANE mutation who had atypical clinical manifestations. For a more accurate diagnosis and treatment of severe chronic neutropenia, further studies are needed to elucidate the various clinical features of ELANE. |
format | Online Article Text |
id | pubmed-10390272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Journal of Yeungnam Medical Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-103902722023-08-01 Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report Kim, Juhyung Hwang, Soyoon Hwang, Narae Lee, Yeonji Cho, Hee Jeong Moon, Joon Ho Sohn, Sang Kyun Baek, Dong Won J Yeungnam Med Sci Case Report Severe chronic neutropenia is classified as severe congenital, cyclic, autoimmune, or idiopathic. However, there is a lot of uncertainty regarding the diagnosis of severe congenital neutropenia (SCN) and chronic idiopathic neutropenia, and this uncertainty affects further evaluations and treatments. A 20-year-old man presented with fever and knee abrasions after a bicycle accident. On admission, his initial absolute neutrophil count (ANC) was 30/µL. He had no medical history of persistent severe neutropenia with periodic oscillation of ANC. Although his fever resolved after appropriate antibiotic therapy, ANC remained at 80/µL. Bone marrow (BM) aspiration and biopsy were performed, and a BM smear showed myeloid maturation arrest. Moreover, genetic mutation test results showed a heterozygous missense variant in exon 4 of the neutrophil elastase ELANE: c597+1G>C (pV190-F199del). The patient was diagnosed with SCN. After discharge, we routinely checked his ANC level and monitored any signs of infection with minimum use of granulocyte colony-stimulating factor (G-CSF), considering its potential risk of leukemic transformation. Considering that SCN can be fatal, timely diagnosis and appropriate management with G-CSF are essential. We report the case of a patient with SCN caused by ELANE mutation who had atypical clinical manifestations. For a more accurate diagnosis and treatment of severe chronic neutropenia, further studies are needed to elucidate the various clinical features of ELANE. Journal of Yeungnam Medical Science 2022-07-28 /pmc/articles/PMC10390272/ /pubmed/35899327 http://dx.doi.org/10.12701/jyms.2022.00353 Text en Copyright © 2023 Yeungnam University College of Medicine, Yeungnam University Institute of Medical Science https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kim, Juhyung Hwang, Soyoon Hwang, Narae Lee, Yeonji Cho, Hee Jeong Moon, Joon Ho Sohn, Sang Kyun Baek, Dong Won Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report |
title | Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report |
title_full | Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report |
title_fullStr | Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report |
title_full_unstemmed | Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report |
title_short | Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report |
title_sort | severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390272/ https://www.ncbi.nlm.nih.gov/pubmed/35899327 http://dx.doi.org/10.12701/jyms.2022.00353 |
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