Progressive symmetric eritrocarotodermia Gottron: A rare case

The article deals with ethiopathogenetic factors of origin of progredient symmetric erythrokeratodermia of Gottron which is mainly characterized by autosomal dominant mode of inheritance and is classified as a disorder of cornification with extra epidermal cellular proliferation.Clinicopathologic cr...

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Bibliographic Details
Main Authors: M. M. Tlish (Author), N. L. Sycheva (Author), N. A. Boyko (Author), M. E. Shavilova (Author), F. A. Psavok (Author)
Format: Book
Published: State Scientific Center of Dermatovenereology and Cosmetology, 2019-10-01T00:00:00Z.
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Summary:The article deals with ethiopathogenetic factors of origin of progredient symmetric erythrokeratodermia of Gottron which is mainly characterized by autosomal dominant mode of inheritance and is classified as a disorder of cornification with extra epidermal cellular proliferation.Clinicopathologic criteria on the basis of which this pathology can be verified are described here, such as: onset of a disease at an early age, strictly divided polycyclic, fixed, hyperkeratotic plaques with a narrow erythematic crown and a clean-cut, sometimes hyper pigmented edge, which are symmetrically located on skin on head, buttocks, limbs and are not prone to quick peripheral growth; large frequency of palmoplantar keratoderma and also histological changes typical of erythrokeratodermia.The article describes a rare clinical case of autosomal-recessive progredient symmetric erythrokeratodermia of Gottron which is distinguished by seasonal changes of skin pathological process - emergence of rash in winter and complete remissions in summer.
Item Description:0042-4609
2313-6294
10.25208/0042-4609-2019-95-3-40-45