Acta Dermato-Venereologica (Feb 2021)

Porokeratosis Plantaris, Palmaris et Disseminata Caused by Con- genital Pathogenic Variants in the MVD Gene and Loss of Hetero­zygosity in Affected Skin

  • Sabine Jägle,
  • Hazem A. Juratli,
  • Geoffroy Hickman,
  • Kira Süssmuth,
  • Maria C. Boente,
  • Julia Kopp,
  • Peter Kirchmeier,
  • Andreas Zimmer,
  • Rudolf Happle,
  • Emmanuelle Bourrat,
  • Henning Hamm,
  • Judith Fischer

DOI
https://doi.org/10.2340/00015555-3753
Journal volume & issue
Vol. 101, no. 2
p. adv00397

Abstract

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Porokeratoses are a heterogeneous group of keratinization disorders. For linear porokeratosis and disseminated superficial actinic porokeratosis, a heterozygous pathogenic germline variant in a mevalonate pathway gene and a postzygotic second hit mutation present in affected skin have been shown to be the patho­genetic mechanism for the development of the lesions. However, the molecular mechanism leading to development of porokeratosis plantaris, palmaris et disseminata is not known. This study analysed a cohort of 4 patients with linear porokeratosis and 3 patients with porokeratosis plantaris, palmaris et disseminata, and performed mutation analyses of DNA extracted from blood samples and skin biopsies. All of the study patients carried the heterozygous germline variant c.70+5G>A in the MVD gene. Loss of heterozygosity due to a second hit mutation was found in affected skin of 3 patients with linear porokeratosis and 2 patients with porokeratosis plantaris, palmaris et disseminata. These results suggest that porokeratosis plantaris, palmaris et disseminata shares the same pathogenetic mechanism as other porokeratosis subtypes and belongs to the phenotypic spectrum of MVD-associated porokeratosis.

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