Chronic recurrent multifocal osteomyelitis in association with pyoderma gangraenosum.

Background: Chronic recurrent multifocal osteomyelitis (CRMO) is a rare acquired inflammatory skeletal disorder of unknown origin. CRMO was first described by Gideon in 1972 and mainly affects children and young adults of female gender. The CRMO is part of the clinical picture of non-bacterial Osteo...

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Publicado en:BMC Oral Health Vol. 16; pp. 1 - 8
Autores principales: Wurm, Matthias Christian, Brecht, Ines, Lell, Michael, Brunner, Kathrin, Mitsimponas, Konstantinos Theodorou, Chada, Martin, Jahn, Julia, Neukam, Friedrich-Wilhelm, von Wilmowsky, Cornelius
Formato: case study diagnostic images pictorial Journal Article
Publicado: BioMed Central 9/1/2016
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 9/1/2016
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      pub: BioMed Central
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        10.1186/s12903-016-0275-z
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        atl: Chronic recurrent multifocal osteomyelitis in association with pyoderma gangraenosum.
      aug:
        au:
          Wurm, Matthias Christian
          Brecht, Ines
          Lell, Michael
          Brunner, Kathrin
          Mitsimponas, Konstantinos Theodorou
          Chada, Martin
          Jahn, Julia
          Neukam, Friedrich-Wilhelm
          von Wilmowsky, Cornelius
        affil: Department of Oral and Maxillofacial Surgery, University of Erlangen-Nürnberg, Glückstrasse 11, 91054 Erlangen, Germany
      sug:
        subj:
          Recurrence
          Osteomyelitis Diagnosis
          Pyoderma Gangrenosum
          Mandible Pathology
          Osteomyelitis Symptoms
          Adolescence
          Female
          Germany
          C-Reactive Protein Blood
          Blood Sedimentation
          Adolescent: 13-18 years
          Female
      ab: Background: Chronic recurrent multifocal osteomyelitis (CRMO) is a rare acquired inflammatory skeletal disorder of unknown origin. CRMO was first described by Gideon in 1972 and mainly affects children and young adults of female gender. The CRMO is part of the clinical picture of non-bacterial Osteomyelitis (NBO) and typically presents a relapsing recurring course with both remission and spontaneous exacerbation. CRMO is typically encountered in the limbs and the metaphysis of long bones in particular. Usually the clinical symptoms include painful swellings of the affected regions. This case report describes the rare case of a CRMO of the mandible in association with pyoderma gangraenosum. Case presentation: A 14-year old female caucasian patient, residing in the south of Germany, presented in the oncological outpatient clinic of our Department of Paediatrics and Adolescent Medicine in June 2014 complaining of increasing neck pain and progressive swelling at her left cheek ongoing for about 6 weeks. These symptoms had been occurring quarterly for 4 years, but had never been as pronounced. Blood biochemistry showed a moderately elevated CRP (35 mg/l) and a significantly increased blood sedimentation rate (BSR 48/120 mm). The panoramic radiograph, however, revealed a bone alteration in the left mandibular region. Further investigations confirmed the diagnosis of CRMO. Conclusion: The present case underlines the fact that rare diseases might occasionally present with even more rare symptoms. These occasions can obviously be considered to present a considerable diagnostic challenge.
      pubtype: Academic Journal
      doctype:
        case study
        diagnostic images
        pictorial
        Journal Article
      ougenre: Article
    language: English
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