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一例可变性红斑角化病:棘层肥厚的表皮中缝隙连接松散。

A case of erythrokeratoderma variabilis: loosened gap junctions in the acanthotic epidermis.

作者信息

Tamaki Yukiko, Tamaki Eiko, Sakai Rie, Takahashi Kenzo, Horiguchi Yuji

机构信息

Department of Dermatology, Osaka Red Cross Hospital, Osaka, Japan.

出版信息

J Dermatol. 2006 Jun;33(6):419-23. doi: 10.1111/j.1346-8138.2006.00099.x.

Abstract

A 15-year-old Japanese female without contributory personal or family medical history had demonstrated irregular, keratotic plaques in the lower extremities since infancy that had been gradually enlarging. The keratotic plaques showed partial erythematous change, which altered shape over a relatively short period, leaving pigmentation. The biopsy specimen taken from the erythematous, keratotic plaque showed typical church-spire-like papillomatosis with acanthosis, and thickening of granular and horny layers. Gene analysis targeting connexin 30.3 and 31, based on the diagnosis of erythrokeratoderma variabilis, did not demonstrate any abnormality of these genes. However, ultrastructural observation disclosed an increased amount of gap junctions, some of which showed four layers on high-powered electron microscopy, suggesting loosened connection of the plasma membrane of the keratinocytes through the gap junctions. This loosened gap junction structure was also observed in a case of lamellar ichthyosis, examined as a reference. The disturbed cell-to-cell interaction through latent damage to the gap junctions may be related to the keratotic changes of the epidermis in these skin diseases.

摘要

一名15岁的日本女性,个人及家族均无相关病史,自婴儿期起双下肢出现不规则角化性斑块,且逐渐增大。角化性斑块呈现部分红斑改变,在相对较短的时间内形状改变,并遗留色素沉着。取自红斑角化性斑块的活检标本显示典型的教堂尖顶样乳头瘤病,伴有棘层肥厚、颗粒层和角质层增厚。基于可变性红斑角化病的诊断,针对连接蛋白30.3和31的基因分析未显示这些基因有任何异常。然而,超微结构观察发现缝隙连接数量增加,其中一些在高倍电子显微镜下显示为四层,提示角质形成细胞的质膜通过缝隙连接的连接松弛。作为对照检查的一例板层状鱼鳞病中也观察到这种缝隙连接结构松弛的情况。通过缝隙连接潜在损伤导致的细胞间相互作用紊乱可能与这些皮肤病中表皮的角化改变有关。

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