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Congenital acute megakaryocytic leukemia
Congenital leukemia (CL) is an extremely rare disorder in the newborn, significant proportion of which is of myeloid origin, primarily of M4 or M5 morphology. As compared to pediatric leukemia, CL is a more aggressive disease. Acute myeloid leukemia (AML-M7) or acute megakaryocytic leukemia is a rar...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342726/ https://www.ncbi.nlm.nih.gov/pubmed/22557786 http://dx.doi.org/10.4103/0971-5851.92821 |
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author | Mathur, N. B. Joshi, Neha Singh, T. Singh, Meeta |
author_facet | Mathur, N. B. Joshi, Neha Singh, T. Singh, Meeta |
author_sort | Mathur, N. B. |
collection | PubMed |
description | Congenital leukemia (CL) is an extremely rare disorder in the newborn, significant proportion of which is of myeloid origin, primarily of M4 or M5 morphology. As compared to pediatric leukemia, CL is a more aggressive disease. Acute myeloid leukemia (AML-M7) or acute megakaryocytic leukemia is a rare type of AML with an incidence of 0.5 per million per year. Median age of presentation is 6 years, and children may present with a broad variety of symptoms including low-grade fever, diarrhea, easy bruising, failure to gain weight and life-threatening conditions. |
format | Online Article Text |
id | pubmed-3342726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33427262012-05-03 Congenital acute megakaryocytic leukemia Mathur, N. B. Joshi, Neha Singh, T. Singh, Meeta Indian J Med Paediatr Oncol Case Report Congenital leukemia (CL) is an extremely rare disorder in the newborn, significant proportion of which is of myeloid origin, primarily of M4 or M5 morphology. As compared to pediatric leukemia, CL is a more aggressive disease. Acute myeloid leukemia (AML-M7) or acute megakaryocytic leukemia is a rare type of AML with an incidence of 0.5 per million per year. Median age of presentation is 6 years, and children may present with a broad variety of symptoms including low-grade fever, diarrhea, easy bruising, failure to gain weight and life-threatening conditions. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3342726/ /pubmed/22557786 http://dx.doi.org/10.4103/0971-5851.92821 Text en Copyright: © Indian Journal of Medical and Paediatric Oncology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Mathur, N. B. Joshi, Neha Singh, T. Singh, Meeta Congenital acute megakaryocytic leukemia |
title | Congenital acute megakaryocytic leukemia |
title_full | Congenital acute megakaryocytic leukemia |
title_fullStr | Congenital acute megakaryocytic leukemia |
title_full_unstemmed | Congenital acute megakaryocytic leukemia |
title_short | Congenital acute megakaryocytic leukemia |
title_sort | congenital acute megakaryocytic leukemia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342726/ https://www.ncbi.nlm.nih.gov/pubmed/22557786 http://dx.doi.org/10.4103/0971-5851.92821 |
work_keys_str_mv | AT mathurnb congenitalacutemegakaryocyticleukemia AT joshineha congenitalacutemegakaryocyticleukemia AT singht congenitalacutemegakaryocyticleukemia AT singhmeeta congenitalacutemegakaryocyticleukemia |