Reticulate acropigmentation of Kitamura

Authors

  • W.A.D. GRIFFITHS

    1. St John's Hospital for Diseases of the Skin, Lisle Street, London WC2H 7BJ
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    • University Department of Dermatology, Liverpool Royal Infirmary, Pembroke Place, Liverpool L3 5PU.


SUMMARY

Seven cases of reticulate acropigmentation of Kitamura (RAPK) are described. All the patients were female and the pattern of inheritance suggested an autosomal dominant mode. Histologically, RAPK is characterized by epidermal atrophy, an increased number of basal melanocytes and the absence of pigmentary incontinence in the upper dermis. The present cases, from Asia, Africa and Europe, are the first to be described outside Japan.

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