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...
| Publicado en: | Pediatric Radiology Vol. 50; no. 5; pp. 618 - 628 |
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| Autores principales: | , , |
| Formato: | review Journal Article |
| Publicado: |
Springer Nature
May2020
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| 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 |
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