Indian Journal of Paediatric Dermatology (Jan 2019)

A rare phenomenon of twin spotting: Phacomatosis pigmentokeratotica

  • Vaishali Wankhade,
  • Vrutika Hasmukh Shah,
  • Rajesh P Singh,
  • Jayesh Mukhi

DOI
https://doi.org/10.4103/ijpd.IJPD_98_18
Journal volume & issue
Vol. 20, no. 3
pp. 267 – 270

Abstract

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Phacomatosis pigmentokeratotica is a rare form of cutaneous mosaicism characterized by epidermal nevus usually nevus sebaceous, papular speckled lentiginous nevus, and extracutaneous anomalies. This type of twin-spot phenomenon (didymosis) is due to postzygotic crossing-over resulting in two homozygous daughter cells, representing the stem cells of the two distinct types of nevi and leading to additional extracutaneous defects. We report a case of this rare syndrome in a 4-year-old male child associated with skeletal anomalies.

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