Literature DB >> 10725816

Phacomatosis pigmentokeratotica: another epidermal nevus syndrome and a distinctive type of twin spotting.

M C Boente1, N Pizzi de Parra, M Larralde de Luna, H B Bonet, A Santos Muñoz, V Parra, P Gramajo, S Moreno, R A Asial.   

Abstract

The name epidermal nevus syndrome could be applied to a group of clinically and histopathologically different entities as has been pointed out by Happle. Phacomatosis pigmentokeratotica is a further type of epidermal nevus syndrome distinguished by the presence of a sebaceous nevus and a contralateral speckled lentiginous nevus of the papular type, associated with skeletal or neurological abnormalities. Three new cases of this recently delineated syndrome are presented. A common origin may account for the temporal and spatial relationship between the epidermal and the speckled lentiginous nevus. The concept of melanocytic-epidermal twin spotting similar to the interpretation of vascular twin spotting could explain the pathogenesis of this entity.

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Year:  2000        PMID: 10725816

Source DB:  PubMed          Journal:  Eur J Dermatol        ISSN: 1167-1122            Impact factor:   3.328


  3 in total

Review 1.  Genodermatoses caused by genetic mosaicism.

Authors:  M Vreeburg; M A M van Steensel
Journal:  Eur J Pediatr       Date:  2012-11-01       Impact factor: 3.183

2.  Phacomatosis pigmentokeratotica without extracutaneous abnormalities: a case study involving a preterm baby.

Authors:  Ga Na Oh; Jong Yeob Kim; Jae Eun Choi; Hyo Hyun Ahn; Young Chul Kye; Soo Hong Seo
Journal:  J Korean Med Sci       Date:  2012-10-30       Impact factor: 2.153

3.  Combined melanocytic and sweat gland neoplasm: cell subsets harbor an identical HRAS mutation in phacomatosis pigmentokeratotica.

Authors:  Janet Y Li; Michael F Berger; Ashfaq Marghoob; Umesh K Bhanot; Jennifer P Toyohara; Melissa P Pulitzer
Journal:  J Cutan Pathol       Date:  2014-07-09       Impact factor: 1.587

  3 in total

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