Literature DB >> 17542865

Linear and whorled hypermelanosis.

Vito Di Lernia1.   

Abstract

Linear and whorled nevoid hypermelanosis is a sporadic pigmentary anomaly occurring within the first weeks of life, characterized clinically by swirls and streaks of macular hyperpigmentation following the lines of Blaschko. Histologically it shows only epidermal melanosis. Underlying chromosomal mosaicism has been demonstrated in only a few published cases. Progressive cribriform and zosteriform hyperpigmentation is considered to be the localized variant of linear and whorled nevoid hypermelanosis. We report a retrospective study on 16 children referred consecutively over a 10-year period for evaluation of segmental, linear or swirled hyperpigmentation distributed along the lines of Blashko, consistent with a diagnosis of linear and whorled nevoid hypermelanosis. Associated abnormalities were found only in one out of six patients with the diffuse form (linear and whorled nevoid hypermelanosis-type) and in none of the remaining 10 children presenting the unilateral form (progressive cribriform and zosteriform hyperpigmentation-type). A long-term follow-up did not disclose further abnormalities. The authors discuss the nosologic position of this entity with respect to hypomelanosis of Ito. Linear and whorled nevoid hypermelanosis and hypomelanosis of Ito should be not considered single entities, but be rather grouped as a heterogeneous collection of nonspecific pigmentary disorders caused by genetic mosaicism. Skin findings in these diseases can differ according to the pigmentation in the normal cell line and whether the second line contains more or less melanosomes than the normal skin of the individual exhibiting mosaicism.

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Year:  2007        PMID: 17542865     DOI: 10.1111/j.1525-1470.2007.00387.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  12 in total

1.  Transient Zebra-like Hyperpigmentation in a Healthy Newborn.

Authors:  Angéla Meszes; Csilla Korponyai; Hajnalka Orvos; Zsanett Csoma
Journal:  Indian J Pediatr       Date:  2015-12-04       Impact factor: 1.967

Review 2.  [Pigmented macules as possible early signs of genetic syndromes].

Authors:  H Hamm; K Emmerich; J Olk
Journal:  Hautarzt       Date:  2019-07       Impact factor: 0.751

Review 3.  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

4.  Linear and Whorled Nevoid Hypermelanosis With Tetralogy of Fallot.

Authors:  Takamichi Ito; Yuichi Yoshida; Hiroyuki Goto; Masutaka Furue; Osamu Yamamoto
Journal:  Indian J Dermatol       Date:  2015 May-Jun       Impact factor: 1.494

5.  [Congenital nevi in childhood].

Authors:  R Wälchli; M Theiler; K Neuhaus; L Weibel
Journal:  Hautarzt       Date:  2013-01       Impact factor: 0.751

6.  Progressive cribriform and zosteriform hyperpigmentation: Where are we at present?

Authors:  Tarang Goyal
Journal:  Indian Dermatol Online J       Date:  2013-10

7.  Progressive cribriform and zosteriform hyperpigmentation.

Authors:  Rameshwar M Gutte
Journal:  Indian Dermatol Online J       Date:  2014-01

8.  Do you know this syndrome? Dyspigmentation along the Blaschko lines caused by trisomy 7 mosaicism.

Authors:  Miguel Pinto de Gouveia; Inês Coutinho; Vera Teixeira; Renata d'Oliveira; Margarida Venâncio; Ana Moreno
Journal:  An Bras Dermatol       Date:  2016 Nov-Dec       Impact factor: 1.896

9.  Hypomelanosis of Ito with Multiple Congenital Anomalies.

Authors:  Da-Ae Yu; Ohsang Kwon; Kyu Han Kim
Journal:  Ann Dermatol       Date:  2019-08-30       Impact factor: 1.444

10.  The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study.

Authors:  Sirisha Varala; Renu George; Lydia Mathew; Paul Russell; Beena Koshy; Samuel P Oommen; Maya Thomas; Karthik Muthusamy; Sangeetha Yoganathan; L Jeyaseelan; Jayaprakash Muliyil
Journal:  Indian Dermatol Online J       Date:  2021-01-16
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