Longitudinal Dental Management of Hypophosphatemic Rickets

  • IDE Masamichi
    Department of Pediatric Dentistry, Tsurumi University School of Dental Medicine
  • KOGUSHI Nobuo
    Nobu Infant and Pediatric Dental Clinic
  • ASADA Yoshinobu
    Department of Pediatric Dentistry, Tsurumi University School of Dental Medicine

Bibliographic Information

Other Title
  • 長期歯科的管理を行ったX連鎖性低リン血症性くる病の1例
  • Case Report

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Description

Hypophosphatemic rickets (HR) is a rare hereditary disease in which spontaneous formation of a gingival abscess (GA) is a dental problem. This report describes longitudinal dental management of a child with HR from primary to permanent dentition.A 2-year-1-month-old boy with HR visited our pediatric dentistry clinic complaining of pain and swelling in the gingiva in the area of the maxillary left primary central incisor. Although caries was detected in that tooth, the extent was not considered severe enough to cause apical periodontitis existing in the same tooth. Since resorption and destruction of periodontal tissue were minimal, root canal treatment was performed. Eventually, GA formation occurred in a total of 17 primary teeth, of which 2 were indicated for extraction and the remaining 15 for root canal treatment. Formation of GA recurred in 4 of those teeth after root canal filling, thus that was repeated. All primary teeth that underwent root canal treatment maintained their function until the eruption stage of the successive permanent teeth, which then received prophylactic treatment. Normal permanent dentition was thus attained without occurrence of caries and GA.Our findings indicate that root canal treatment may be an effective treatment method for children with HR whose primary teeth are complicated with GA. Furthermore, instead of extraction, root canal treatment should be considered as the first choice of treatment for cases with minimal root resorption and periodontal tissue damage.

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Details 詳細情報について

  • CRID
    1390001205519900160
  • NII Article ID
    10031121929
  • NII Book ID
    AN00116228
  • DOI
    10.11411/jspd.50.4_313
  • ISSN
    21865078
    05831199
  • Text Lang
    ja
  • Data Source
    • JaLC
    • CiNii Articles
  • Abstract License Flag
    Disallowed

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