Familial linear and whorled nevoid hypermelanosis

Masashi Akiyama, Akihiko Aranami, Yuko Sasaki, Tamotsu Ebihara, Makoto Sugiura

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Two patients with familial linear and whorled nevoid hypemelanosis, a 33-year-old woman and her 3-month-old daughter, are described. These are the first cases of linear and whorled nevoid hypermelanosis of familial occurrence reported in the literature. Asymptomatic hyperpigmented macules in streaky configurations had appeared on the trunk and extremities of both patients several weeks after birth and then gradually spread. No previous inflammation or eruption was observed. Histologic examination revealed a slight increase in the number of melanocytes in the epidermis and an irregular basal melanosis. No pigmentary incontinence or melanophages were observed in the dermis. Ultrastructurally the only finding was an increase in the number of normal-appearing mature melanosomes in, keratinocytes in the lesion. Chromosomal analysis of cultured peripheral blood lymphocytes and dermal fibroblasts from normal and pigmented skin revealed no evidence of mixoploidy or chimerism. An undescribed genetic abnormality is suggested as the cause.

Original languageEnglish
Pages (from-to)831-833
Number of pages3
JournalJournal of the American Academy of Dermatology
Volume30
Issue number5
DOIs
Publication statusPublished - 1994 Jan 1

ASJC Scopus subject areas

  • Dermatology

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