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A particular subtype of ichthyosis congenita type III. Clinical, light, and electron microscopic features.

作者信息

de Wolf K, Gourdain J M, Dobbeleer G D, Song M

机构信息

Department of Dermatology, St. Pierre-Brugmann University Hospitals, Brussels, Belgium.

出版信息

Am J Dermatopathol. 1995 Dec;17(6):606-11. doi: 10.1097/00000372-199512000-00015.

DOI:10.1097/00000372-199512000-00015
PMID:8599478
Abstract

We report the case of a second patient with the extraordinary ultrastructural findings of vacuolated structures intermingled with membranes in the perinuclear part of the upper epidermal cells. Clinical, light microscopic, and electron microscopic features of this particular presentation of ichthyosis congenita type III have already been presented by K. M. Niemi and L. Kanerva in 1989. Although our patient has more or less the same light and electron microscopic findings, the clinical picture is more severe. The patient was born as a collodion baby. Later, he showed signs of generalized severe involvement with large scales, erythrodermia, and itching. Successful therapy with retinoids resulted in complete removal of the hyperkeratosis but left the striking reticulate skin pattern. Noting the heterogeneous clinical presentation, the specific electron microscopic findings are diagnostic. No biochemical data on this disease are known.

摘要

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