Literature DB >> 3522665

Ichthyosis bullosa of Siemens: a unique type of epidermolytic hyperkeratosis.

H Traupe, G Kolde, H Hamm, R Happle.   

Abstract

We report the second family of ichthyosis bullosa, an entity that was first described by Siemens in 1937 and since then has fallen into oblivion. Clinically, ichthyosis bullosa is characterized by blistering resembling epidermolysis bullosa simplex and by generalized, yet circumscribed dark gray hyperkeratoses covering mainly the arms and the legs. Lichenification and superficially denuded areas (mauserung) are further prominent features. Histology disclosed intracorneal blister formation corresponding to the mauserung phenomenon and epidermolytic hyperkeratosis that was confined to the granular layer and to the uppermost layers of the prickle cells. On electron microscopic examination the keratinocytes of these layers displayed structural alterations of tonofilaments as usually observed in epidermolytic hyperkeratosis. Thus ichthyosis bullosa shares with bullous ichthyosiform erythroderma blistering and epidermolytic hyperkeratosis, but can be distinguished from this wellknown disease by the lack of erythroderma, by the mauserung phenomenon, by the confinement of acanthokeratolysis to the superficial layers of the epidermis, and by intracorneal blistering.

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Year:  1986        PMID: 3522665     DOI: 10.1016/s0190-9622(86)70123-0

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  8 in total

1.  [The ichthyoses. Pathophysiological models of epidermal differentiation].

Authors:  D Hohl; M Huber
Journal:  Hautarzt       Date:  2013-01       Impact factor: 0.751

2.  Elevated levels of soluble CD8 antigen in sera of patients with psoriasis--a possible sign of suppressor/cytotoxic T-cell activation.

Authors:  A Kapp
Journal:  Arch Dermatol Res       Date:  1990       Impact factor: 3.017

3.  Genetics of dark skin in mice.

Authors:  Karen R Fitch; Kelly A McGowan; Catherine D van Raamsdonk; Helmut Fuchs; Daekee Lee; Anne Puech; Yann Hérault; David W Threadgill; Martin Hrabé de Angelis; Gregory S Barsh
Journal:  Genes Dev       Date:  2003-01-15       Impact factor: 11.361

Review 4.  The molecular basis for inherited bullous diseases.

Authors:  B P Korge; T Krieg
Journal:  J Mol Med (Berl)       Date:  1996-02       Impact factor: 4.599

5.  Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.

Authors:  Lisa Heinz; Gwang-Jin Kim; Slaheddine Marrakchi; Julie Christiansen; Hamida Turki; Marc-Alexander Rauschendorf; Mark Lathrop; Ingrid Hausser; Andreas D Zimmer; Judith Fischer
Journal:  Am J Hum Genet       Date:  2017-06-01       Impact factor: 11.025

Review 6.  Ichthyoses-A Clinical and Pathological Spectrum from Heterogeneous Cornification Disorders to Inflammation.

Authors:  Dieter Metze; Heiko Traupe; Kira Süßmuth
Journal:  Dermatopathology (Basel)       Date:  2021-05-07

Review 7.  Updated molecular genetics and pathogenesis of ichthiyoses.

Authors:  Masashi Akiyama
Journal:  Nagoya J Med Sci       Date:  2011-08       Impact factor: 1.131

8.  Deep Phenotyping of Superficial Epidermolytic Ichthyosis due to a Recurrent Mutation in KRT2.

Authors:  Yuika Suzuki; Takuya Takeichi; Kana Tanahashi; Yoshinao Muro; Yasushi Suga; Tomoo Ogi; Masashi Akiyama
Journal:  Int J Mol Sci       Date:  2022-07-14       Impact factor: 6.208

  8 in total

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