Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins.

Caffey disease, or infantile cortical hyperostosis, classically describes a self-limited inflammatory disorder that presents in the infant with fussiness, focal swelling and sometimes fever. Imaging is conventionally limited to radiography, which shows mild to profound subperiosteal bone formation a...

Descripción completa

Detalles Bibliográficos
Publicado en:Pediatric Radiology Vol. 50; no. 5; pp. 618 - 628
Autores principales: Chapman, Teresa, Menashe, Sarah J., Taragin, Benjamin H.
Formato: review Journal Article
Publicado: Springer Nature May2020
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=142685123&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 142685123
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        03010449
        O03
      jtl: Pediatric Radiology
      issn: 03010449
      maglogo: N
    pubinfo:
      dt: May2020
      vid: 50
      iid: 5
      pid: 237
      pub: Springer Nature
      place: New York, New York
    artinfo:
      ui:
        142685123
        142685123
        NLM31873763
        142685123
        10.1007/s00247-019-04590-3
        NLM31873763
        142685123
      ppf: 618
      ppct: 10
      formats:
        fmt:
          – @attributes:
              type: T
          – @attributes:
              type: P
      tig:
        atl: Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins.
      aug:
        au:
          Chapman, Teresa
          Menashe, Sarah J.
          Taragin, Benjamin H.
        affil: Department of Radiology, Seattle Children's Hospital, University of Washington School of Medicine, Campus Box 359300, 1959 NE Pacific St., 98195, Seattle, WA, USA
      sug:
        subj:
          Hyperostosis, Cortical Congenital
          Magnetic Resonance Imaging Methods
          Radiography Methods
          Osteomyelitis
          Male
          Infant, Newborn
          Female
          Diagnosis, Differential
          Child
          Child, Preschool
          Infant
          Recurrence
          Bone and Bones
          Questionnaires
          Infant, Newborn: birth-1 month
          Child: 6-12 years
          Child, Preschool: 2-5 years
          Infant: 1-23 months
          Male
          Female
      ab: Caffey disease, or infantile cortical hyperostosis, classically describes a self-limited inflammatory disorder that presents in the infant with fussiness, focal swelling and sometimes fever. Imaging is conventionally limited to radiography, which shows mild to profound subperiosteal bone formation and sometimes deformity. This disease was not uncommonly diagnosed in the late 20th century. Interestingly, the disease may not just occur in the infant, and it may be due to a genetic mutation in the alpha-one chain of type 1 collagen (COL1A1). Recurrent or delayed onset in the older child or adolescent also occurs. In more recent years, another type of inflammatory bone disorder, chronic sterile osteomyelitis, has been frequently recognized and, depending on the radiographic stage or the diagnostic modality used, may have characteristics overlapping with Caffey disease. In this review, we discuss the demographics, imaging and known etiologies for Caffey disease and chronic recurrent multifocal osteomyelitis and raise the possibility of similar molecular origins.
      pubtype: Academic Journal
      doctype:
        review
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N