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EAHP 2020 workshop proceedings, pediatric myeloid neoplasms

Leguit, R. J. ; Orazi, A. ; Kucine, N. ; Kvasnicka, H. M. ; Gianelli, U. ; Arber, D. A. ; Porwit, A. LU and Ponzoni, M. (2022) In Virchows Archiv 481(4). p.621-646
Abstract

The first section of the bone marrow workshop of the European Association of Haematopathology 2020 Virtual Meeting was dedicated to pediatric myeloid neoplasms. The section covered the whole spectrum of myeloid neoplasms, including myelodysplastic syndromes (MDS), myeloproliferative neoplasms (MPN), myelodysplastic/myeloproliferative neoplasms (MDS/MPN), and acute myeloid leukemia. The workshop cases are hereby presented, preceded by an introduction on these overall rare diseases in this age group. Very rare entities such as primary myelofibrosis, pediatric MDS with fibrosis, and MDS/MPN with JMML-like features and t(4;17)(q12;q21); FIP1L1::RARA fusion, are described in more detail.

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author
; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Acute leukemia, Bone marrow biopsy, EAHP workshop, Juvenile myelomonocytic leukemia, Myelodysplastic syndrome, Myeloproliferative neoplasm, Pediatric
in
Virchows Archiv
volume
481
issue
4
pages
26 pages
publisher
Springer
external identifiers
  • scopus:85134239668
  • pmid:35819517
ISSN
0945-6317
DOI
10.1007/s00428-022-03375-8
language
English
LU publication?
yes
id
c4ca068b-a65c-41fd-ba29-b3b9163406c3
date added to LUP
2022-10-04 08:51:28
date last changed
2024-06-13 16:01:45
@article{c4ca068b-a65c-41fd-ba29-b3b9163406c3,
  abstract     = {{<p>The first section of the bone marrow workshop of the European Association of Haematopathology 2020 Virtual Meeting was dedicated to pediatric myeloid neoplasms. The section covered the whole spectrum of myeloid neoplasms, including myelodysplastic syndromes (MDS), myeloproliferative neoplasms (MPN), myelodysplastic/myeloproliferative neoplasms (MDS/MPN), and acute myeloid leukemia. The workshop cases are hereby presented, preceded by an introduction on these overall rare diseases in this age group. Very rare entities such as primary myelofibrosis, pediatric MDS with fibrosis, and MDS/MPN with JMML-like features and t(4;17)(q12;q21); FIP1L1::RARA fusion, are described in more detail.</p>}},
  author       = {{Leguit, R. J. and Orazi, A. and Kucine, N. and Kvasnicka, H. M. and Gianelli, U. and Arber, D. A. and Porwit, A. and Ponzoni, M.}},
  issn         = {{0945-6317}},
  keywords     = {{Acute leukemia; Bone marrow biopsy; EAHP workshop; Juvenile myelomonocytic leukemia; Myelodysplastic syndrome; Myeloproliferative neoplasm; Pediatric}},
  language     = {{eng}},
  number       = {{4}},
  pages        = {{621--646}},
  publisher    = {{Springer}},
  series       = {{Virchows Archiv}},
  title        = {{EAHP 2020 workshop proceedings, pediatric myeloid neoplasms}},
  url          = {{http://dx.doi.org/10.1007/s00428-022-03375-8}},
  doi          = {{10.1007/s00428-022-03375-8}},
  volume       = {{481}},
  year         = {{2022}},
}