論文

査読有り 国際誌
2018年

Leukoderma induced by rhododendrol is different from leukoderma of vitiligo in pathogenesis: A novel comparative morphological study

Journal of Cutaneous Pathology
  • Reiko Tsutsumi
  • ,
  • Kazunari Sugita
  • ,
  • Yuko Abe
  • ,
  • Yutaka Hozumi
  • ,
  • Tamio Suzuki
  • ,
  • Nanako Yamada
  • ,
  • Yuichi Yoshida
  • ,
  • Osamu Yamamoto

46
2
開始ページ
123
終了ページ
129
記述言語
日本語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/cup.13396
出版者・発行元
Wiley

BACKGROUND: Rhododendrol (rhododenol), an inhibitor of tyrosinase activity, is used as a skin-whitening component. Many cases of leukoderma after the application have been reported, termed rhododenol-induced leukoderma (RIL). The aim of this study was to clarify the pathogenesis of RIL morphologically through comparison with vitiligo. METHODS: We examined 14 cases of RIL and 15 cases of vitiligo using routine histopathology and immunohistochemistry. Thirteen cases of RIL, six cases of vitiligo and specimens of the RIL mouse model were evaluated by electron microscopy. RESULTS: There were common findings in RIL and vitiligo at the light-microscopic level: (a) vacuolar changes in the dermo-epidermal junction, (b) melanophages in the papillary dermis, (c) perifollicular lymphocyte infiltration, (d) loss or decrease of basal melanin pigment and (e) decrease of melanocytes in the lesions. The ultrastructural observations showed specific findings of RIL: (a) remaining melanocytes in depigmented lesions, (b) inhomogeneous melanization in melanocytes and (c) degenerated melanosomes in melanocytes. Some of the findings were observed in a RIL mouse model. Furthermore, it is notable that cell organelles of melanocytes were intact in our RIL cases. CONCLUSION: Morphological changes of RIL targeting melanosomes in melanocytes without degeneration of organelles reflect the reversible clinical course of most cases.

リンク情報
DOI
https://doi.org/10.1111/cup.13396
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30456919
ID情報
  • DOI : 10.1111/cup.13396
  • ISSN : 0303-6987
  • ORCIDのPut Code : 69132690
  • PubMed ID : 30456919

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