Literature DB >> 6500934

[Congenital reticular ichthyosiform erythroderma].

S Marghescu, I Anton-Lamprecht, P O Rudolph, R Kaste.   

Abstract

A 57-year-old female patient has had generalized cutaneous lesions since birth. Clinically there are patch- and band-like areas of erythrokeratotic and pigmented skin in reticular arrangement. The most important histological findings are band-like parakeratosis, psoriasiform acanthosis, vacuolization of the keratinocytes in the upper layers of the epidermis with a high frequency of binuclear cells, and deposits of amyloid in the dermis. Ultrastructurally, the formation of perinuclear shells built from a three-dimensional network of fine filaments is the most peculiar finding. Binuclear cells are frequently found from the first suprabasal layers. Oedematization of the perinuclear cytoplasm within the shells finally leads to vacuolization of the uppermost granular cells. The horny layer is parakeratotic and contains debris of nuclei and lipid vacuoles. In the clinically normal appearing skin within the reticular network, keratinization occurs in a completely normal fashion. In spite of a good response to retinoid treatment, perinuclear shells and binuclear cells remain demonstrable in involved regions. The clinical, histological and ultrastructural peculiarities of this case suggest the diagnosis of a special type of congenital disturbances of keratinization, which can be clearly distinguished from the well-known ichthyosiform dermatoses and other inborn errors of keratinization.

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Year:  1984        PMID: 6500934

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  7 in total

1.  Altered keratin expression in ichthyosis hystrix Curth-Macklin. A light and electron microscopic study.

Authors:  K M Niemi; I Virtanen; L Kanerva; M Muttilainen
Journal:  Arch Dermatol Res       Date:  1990       Impact factor: 3.017

2.  Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10.

Authors:  Keith A Choate; Yin Lu; Jing Zhou; Murim Choi; Peter M Elias; Anita Farhi; Carol Nelson-Williams; Debra Crumrine; Mary L Williams; Amy J Nopper; Alanna Bree; Leonard M Milstone; Richard P Lifton
Journal:  Science       Date:  2010-08-26       Impact factor: 47.728

3.  Ichthyosis congenita type III. Clinical and ultrastructural characteristics and distinction within the heterogeneous ichthyosis congenita group.

Authors:  M L Arnold; I Anton-Lamprecht; B Melz-Rothfuss; W Hartschuh
Journal:  Arch Dermatol Res       Date:  1988       Impact factor: 3.017

4.  Clinical, light and electron microscopic features of recessive ichthyosis congenita type III.

Authors:  K M Niemi; L Kanerva; C F Wahlgren; J Ignatius
Journal:  Arch Dermatol Res       Date:  1992       Impact factor: 3.017

5.  Congenital ichthyosis with hypogonadism and growth retardation--a new syndrome with peculiar ultrastructural features.

Authors:  M L Arnold; I Anton-Lamprecht; H Albrecht-Nebe
Journal:  Arch Dermatol Res       Date:  1992       Impact factor: 3.017

6.  Arginine- but not alanine-rich carboxy-termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti.

Authors:  Patricia Renz; Elias Imahorn; Iris Spoerri; Magomet Aushev; Oliver P March; Hedwig Wariwoda; Sarah Von Arb; Andreas Volz; Peter H Itin; Julia Reichelt; Bettina Burger
Journal:  J Cell Mol Med       Date:  2019-10-22       Impact factor: 5.310

Review 7.  Ichthyosis with confetti: clinics, molecular genetics and management.

Authors:  Liliana Guerra; Andrea Diociaiuti; May El Hachem; Daniele Castiglia; Giovanna Zambruno
Journal:  Orphanet J Rare Dis       Date:  2015-09-17       Impact factor: 4.123

  7 in total

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