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High rate of extreme thrombocytosis indicates bone marrow hyperactivity and splenic dysfunction among congenital diaphragmatic hernia patients.
Gu, Hannah; Devine, Matthew; Hedrick, Holly L; Rintoul, Natalie E; Thom, Christopher S.
Afiliação
  • Gu H; Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Devine M; Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Hedrick HL; Department of General Surgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Rintoul NE; Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Thom CS; Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Platelets ; 33(5): 787-789, 2022 Jul 04.
Article em En | MEDLINE | ID: mdl-34697983
ABSTRACT
Pediatric extreme thrombocytosis (EXT, platelet count > 1000 x 103/µL) is rare. In a single center retrospective analysis of hospitalized children with EXT, infants with congenital diaphragmatic hernia (CDH) were overrepresented. In general pediatric patients, EXT is usually secondary to infection or inflammation, but most of the 14 CDH patients with EXT had no identifiable inciting factor. Instead, there was evidence that splenic dysfunction and bone marrow hyperactivity underlied EXT in CDH patients. None were associated with bleeding or thrombosis. Our findings identify mechanisms underlying EXT, and aid clinical interpretation and management of EXT in the pediatric population.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombocitose / Hérnias Diafragmáticas Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombocitose / Hérnias Diafragmáticas Congênitas Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans / Infant Idioma: En Ano de publicação: 2022 Tipo de documento: Article