Pediatric Myelodysplastic Syndrome
Myelodysplastic syndromes (MDSs) are rare in children and have unique clinical manifestations and implications. To review the clinical features, pathogenesis, and classification of pediatric MDS. Published literature and personal experience. Pediatric MDS vastly differs from adult MDS. Evaluation fo...
Gespeichert in:
Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2024-10 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | Archives of pathology & laboratory medicine (1976) |
container_volume | |
creator | Inam, Zaina Pan, Miao Diab, Yaser Schore, Reuven Vatsayan, Anant Cheng, Jinjun |
description | Myelodysplastic syndromes (MDSs) are rare in children and have unique clinical manifestations and implications.
To review the clinical features, pathogenesis, and classification of pediatric MDS.
Published literature and personal experience.
Pediatric MDS vastly differs from adult MDS. Evaluation for the presence of an underlying germline predisposition syndrome is critical for optimal classification and management. Because of the rarity of cases, resources to aid with the recognition, diagnosis, and management of pediatric MDS are limited, and multi-institutional collaborative studies are needed for the future. |
doi_str_mv | 10.5858/arpa.2024-0164-RA |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3114498975</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3114498975</sourcerecordid><originalsourceid>FETCH-LOGICAL-c141a-5453629e704c89da7d49cc58982341af5a8175290a03da40fd1d8a9efa5c0f1c3</originalsourceid><addsrcrecordid>eNo9kMtKxDAUhoMozjj6AG5EXLnJmJNLmyyHwRuMKKOuwzFJodJOa9Iu-va2zOjq8HP-C3yEXAJbKq30HcYWl5xxSRlkkm5XR2QOSgrKIVPHZM4YE9QYrWbkLKXvURrO4ZTMhBG54YbNyc1b8CV2sXTXL0OoGj-ktsLUjfp92PnY1OGcnBRYpXBxuAvy-XD_sX6im9fH5_VqQx1IQKqkEhk3IWfSaeMx99I4p7TRXIz_QqGGXI2jyIRHyQoPXqMJBSrHCnBiQW73vW1sfvqQOluXyYWqwl1o-mQFgJRGm1yNVthbXWxSiqGwbSxrjIMFZic0dkJjJzR2QmO3qzFzdajvv-rg_xN_LMQvn7te3w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3114498975</pqid></control><display><type>article</type><title>Pediatric Myelodysplastic Syndrome</title><source>Allen Press Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Inam, Zaina ; Pan, Miao ; Diab, Yaser ; Schore, Reuven ; Vatsayan, Anant ; Cheng, Jinjun</creator><creatorcontrib>Inam, Zaina ; Pan, Miao ; Diab, Yaser ; Schore, Reuven ; Vatsayan, Anant ; Cheng, Jinjun</creatorcontrib><description>Myelodysplastic syndromes (MDSs) are rare in children and have unique clinical manifestations and implications.
To review the clinical features, pathogenesis, and classification of pediatric MDS.
Published literature and personal experience.
Pediatric MDS vastly differs from adult MDS. Evaluation for the presence of an underlying germline predisposition syndrome is critical for optimal classification and management. Because of the rarity of cases, resources to aid with the recognition, diagnosis, and management of pediatric MDS are limited, and multi-institutional collaborative studies are needed for the future.</description><identifier>ISSN: 0003-9985</identifier><identifier>ISSN: 1543-2165</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/arpa.2024-0164-RA</identifier><identifier>PMID: 39379290</identifier><language>eng</language><publisher>United States</publisher><ispartof>Archives of pathology & laboratory medicine (1976), 2024-10</ispartof><rights>2024 College of American Pathologists.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39379290$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Inam, Zaina</creatorcontrib><creatorcontrib>Pan, Miao</creatorcontrib><creatorcontrib>Diab, Yaser</creatorcontrib><creatorcontrib>Schore, Reuven</creatorcontrib><creatorcontrib>Vatsayan, Anant</creatorcontrib><creatorcontrib>Cheng, Jinjun</creatorcontrib><title>Pediatric Myelodysplastic Syndrome</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>Myelodysplastic syndromes (MDSs) are rare in children and have unique clinical manifestations and implications.
To review the clinical features, pathogenesis, and classification of pediatric MDS.
Published literature and personal experience.
Pediatric MDS vastly differs from adult MDS. Evaluation for the presence of an underlying germline predisposition syndrome is critical for optimal classification and management. Because of the rarity of cases, resources to aid with the recognition, diagnosis, and management of pediatric MDS are limited, and multi-institutional collaborative studies are needed for the future.</description><issn>0003-9985</issn><issn>1543-2165</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtKxDAUhoMozjj6AG5EXLnJmJNLmyyHwRuMKKOuwzFJodJOa9Iu-va2zOjq8HP-C3yEXAJbKq30HcYWl5xxSRlkkm5XR2QOSgrKIVPHZM4YE9QYrWbkLKXvURrO4ZTMhBG54YbNyc1b8CV2sXTXL0OoGj-ktsLUjfp92PnY1OGcnBRYpXBxuAvy-XD_sX6im9fH5_VqQx1IQKqkEhk3IWfSaeMx99I4p7TRXIz_QqGGXI2jyIRHyQoPXqMJBSrHCnBiQW73vW1sfvqQOluXyYWqwl1o-mQFgJRGm1yNVthbXWxSiqGwbSxrjIMFZic0dkJjJzR2QmO3qzFzdajvv-rg_xN_LMQvn7te3w</recordid><startdate>20241008</startdate><enddate>20241008</enddate><creator>Inam, Zaina</creator><creator>Pan, Miao</creator><creator>Diab, Yaser</creator><creator>Schore, Reuven</creator><creator>Vatsayan, Anant</creator><creator>Cheng, Jinjun</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20241008</creationdate><title>Pediatric Myelodysplastic Syndrome</title><author>Inam, Zaina ; Pan, Miao ; Diab, Yaser ; Schore, Reuven ; Vatsayan, Anant ; Cheng, Jinjun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c141a-5453629e704c89da7d49cc58982341af5a8175290a03da40fd1d8a9efa5c0f1c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Inam, Zaina</creatorcontrib><creatorcontrib>Pan, Miao</creatorcontrib><creatorcontrib>Diab, Yaser</creatorcontrib><creatorcontrib>Schore, Reuven</creatorcontrib><creatorcontrib>Vatsayan, Anant</creatorcontrib><creatorcontrib>Cheng, Jinjun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inam, Zaina</au><au>Pan, Miao</au><au>Diab, Yaser</au><au>Schore, Reuven</au><au>Vatsayan, Anant</au><au>Cheng, Jinjun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pediatric Myelodysplastic Syndrome</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><addtitle>Arch Pathol Lab Med</addtitle><date>2024-10-08</date><risdate>2024</risdate><issn>0003-9985</issn><issn>1543-2165</issn><eissn>1543-2165</eissn><abstract>Myelodysplastic syndromes (MDSs) are rare in children and have unique clinical manifestations and implications.
To review the clinical features, pathogenesis, and classification of pediatric MDS.
Published literature and personal experience.
Pediatric MDS vastly differs from adult MDS. Evaluation for the presence of an underlying germline predisposition syndrome is critical for optimal classification and management. Because of the rarity of cases, resources to aid with the recognition, diagnosis, and management of pediatric MDS are limited, and multi-institutional collaborative studies are needed for the future.</abstract><cop>United States</cop><pmid>39379290</pmid><doi>10.5858/arpa.2024-0164-RA</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0003-9985 |
ispartof | Archives of pathology & laboratory medicine (1976), 2024-10 |
issn | 0003-9985 1543-2165 1543-2165 |
language | eng |
recordid | cdi_proquest_miscellaneous_3114498975 |
source | Allen Press Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
title | Pediatric Myelodysplastic Syndrome |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-16T07%3A19%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pediatric%20Myelodysplastic%20Syndrome&rft.jtitle=Archives%20of%20pathology%20&%20laboratory%20medicine%20(1976)&rft.au=Inam,%20Zaina&rft.date=2024-10-08&rft.issn=0003-9985&rft.eissn=1543-2165&rft_id=info:doi/10.5858/arpa.2024-0164-RA&rft_dat=%3Cproquest_cross%3E3114498975%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3114498975&rft_id=info:pmid/39379290&rfr_iscdi=true |