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Primary autoimmune myelofibrosis: A case report in a child
Autoimmune myelofibrosis (AIMF) is an uncommon cause of myelofibrosis associated with favorable outcome. Primary AIMF, AIMF without a known systemic autoimmune disorder, has been described in adults, but never in children. Here, we present, for the first time, an apparent case of primary AIMF in a 1...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175846/ https://www.ncbi.nlm.nih.gov/pubmed/35847714 http://dx.doi.org/10.1002/jha2.38 |
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author | Hexner‐Erlichman, Zufit Yacobovich, Joanne Trougouboff, Philippe Avraham‐Kelbert, Moran Eitam, Harel Spiegel, Ronen Yeganeh, Shay Levin, Carina |
author_facet | Hexner‐Erlichman, Zufit Yacobovich, Joanne Trougouboff, Philippe Avraham‐Kelbert, Moran Eitam, Harel Spiegel, Ronen Yeganeh, Shay Levin, Carina |
author_sort | Hexner‐Erlichman, Zufit |
collection | PubMed |
description | Autoimmune myelofibrosis (AIMF) is an uncommon cause of myelofibrosis associated with favorable outcome. Primary AIMF, AIMF without a known systemic autoimmune disorder, has been described in adults, but never in children. Here, we present, for the first time, an apparent case of primary AIMF in a 15‐year‐old boy admitted with profound hypoproliferative anemia. |
format | Online Article Text |
id | pubmed-9175846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91758462022-07-14 Primary autoimmune myelofibrosis: A case report in a child Hexner‐Erlichman, Zufit Yacobovich, Joanne Trougouboff, Philippe Avraham‐Kelbert, Moran Eitam, Harel Spiegel, Ronen Yeganeh, Shay Levin, Carina EJHaem Case Reports Autoimmune myelofibrosis (AIMF) is an uncommon cause of myelofibrosis associated with favorable outcome. Primary AIMF, AIMF without a known systemic autoimmune disorder, has been described in adults, but never in children. Here, we present, for the first time, an apparent case of primary AIMF in a 15‐year‐old boy admitted with profound hypoproliferative anemia. John Wiley and Sons Inc. 2020-06-28 /pmc/articles/PMC9175846/ /pubmed/35847714 http://dx.doi.org/10.1002/jha2.38 Text en © 2020 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Hexner‐Erlichman, Zufit Yacobovich, Joanne Trougouboff, Philippe Avraham‐Kelbert, Moran Eitam, Harel Spiegel, Ronen Yeganeh, Shay Levin, Carina Primary autoimmune myelofibrosis: A case report in a child |
title | Primary autoimmune myelofibrosis: A case report in a child |
title_full | Primary autoimmune myelofibrosis: A case report in a child |
title_fullStr | Primary autoimmune myelofibrosis: A case report in a child |
title_full_unstemmed | Primary autoimmune myelofibrosis: A case report in a child |
title_short | Primary autoimmune myelofibrosis: A case report in a child |
title_sort | primary autoimmune myelofibrosis: a case report in a child |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175846/ https://www.ncbi.nlm.nih.gov/pubmed/35847714 http://dx.doi.org/10.1002/jha2.38 |
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