Ann Dermatol.  2019 Aug;31(Suppl):S49-S51. 10.5021/ad.2019.31.S.S49.

A Case of Erythrokeratodermia Variabilis in Korean

Affiliations
  • 1Department of Dermatology, Eulji University Hospital, Eulji University School of Medicine, Daejeon, Korea. dwkoo@eulji.ac.kr

Abstract

No abstract available.


MeSH Terms

Erythrokeratodermia Variabilis*

Figure

  • Fig. 1 (A~D) Well demarcated, symmetric erythematous keratotic plaques on both axilla, trunk and buttock, and thigh. (E, F) Thick keratoderma on palm and soles are shown. We received the patient's consent form about publishing all photographic material.

  • Fig. 2 (A) Marked hyperkeratosis and mild acanthosis with mild inflammatory infiltration in upper dermis. Mild increase in number of eccrine glands is shown (left axilla: H&E, ×40). (B) Close up view, compact hyperkeratosis, normal-appearing granular layer and irregular acanthosis in the epidermis with mild perivascular lymphocyte infiltration in the papillary to upper dermis (left axilla: H&E, ×200).


Reference

1. Ishida-Yamamoto A. Erythrokeratodermia variabilis et progressiva. J Dermatol. 2016; 43:280–285.
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2. Common JE, O'Toole EA, Leigh IM, Thomas A, Griffiths WA, Venning V, et al. Clinical and genetic heterogeneity of erythrokeratoderma variabilis. J Invest Dermatol. 2005; 125:920–927.
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3. Balci DD, Yaldiz M. Erythrokeratodermia variabilis: successful palliative treatment with acitretin. Indian J Dermatol Venereol Leprol. 2008; 74:649–650.
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4. Lee JS, Sung YH, Lee JH, Park JK. Erythrokeratodermia variabilis with alopecia universalis. Ann Dermatol. 1990; 2:17–20.
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5. Nam HM, Kim UK, Park K, Park SD. Erythrokeratodermia variabilis with congenital deaf-mutism. Korean J Dermatol. 2011; 49:379–381.
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