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伴有毛发改变的皮肤剥脱综合征

Peeling skin syndrome with hair changes.

作者信息

Mevorah B, Orion E, de Viragh P, Bergman R, Gat A, Legume C, Van Neste D J, Brenner S

机构信息

Department of Dermatology, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Dermatology. 1998;197(4):373-6. doi: 10.1159/000018034.

DOI:10.1159/000018034
PMID:9873177
Abstract

A 13-year-old boy with typical peeling skin syndrome (PSS) is described. The clinical picture corresponded to the inflammatory variant of PSS (type B). In addition, the patient had gross and microscopic hair anomalies such as trichorrhexis invaginata-like changes, irregular hair shaft torsions and moniliform hair shaft diameter reductions. The observed dysmorphic hair changes are discussed and interpreted as being an integral component of the dermatosis in this case. To the best of our knowledge, such hair anomalies have not yet been described in PSS.

摘要

本文描述了一名患有典型剥脱性皮肤综合征(PSS)的13岁男孩。临床表现符合PSS的炎症变体(B型)。此外,该患者存在明显的和显微镜下可见的毛发异常,如套叠性脆发样改变、毛发干不规则扭转和念珠状毛发干直径变细。对观察到的毛发畸形变化进行了讨论,并解释为该病例中皮肤病的一个组成部分。据我们所知,PSS中尚未描述过此类毛发异常。

相似文献

1
Peeling skin syndrome with hair changes.伴有毛发改变的皮肤剥脱综合征
Dermatology. 1998;197(4):373-6. doi: 10.1159/000018034.
2
[Trichorrhexis congenita. Scanning electron microscopic studies on a congenital disorder of hair growth].[先天性毛发干折断。先天性毛发生长障碍的扫描电子显微镜研究]
Hautarzt. 1975 Nov;26(11):576-80.
3
[Neurocutaneous syndrome with hair alterations].[伴有毛发改变的神经皮肤综合征]
Rev Neurol. 1997 Sep;25 Suppl 3:S243-9.
4
A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.一个新的角蛋白丝聚集素基因致病性变异导致弥漫性炎症性剥脱性皮肤综合征伴显著嗜酸性粒细胞增多和发内卷曲。
Pediatr Dermatol. 2022 Mar;39(2):268-272. doi: 10.1111/pde.14939. Epub 2022 Feb 17.
5
Hair shaft videodermoscopy in netherton syndrome.Netherton综合征中的毛干皮肤镜检查
Pediatr Dermatol. 2009 May-Jun;26(3):320-2. doi: 10.1111/j.1525-1470.2008.00778.x.
6
[Netherton's syndrome. Ichthyosis-like changes in the skin and trichorrhexis invaginata. Demonstration of pathologically changed cortex keratin in the hair].
Hautarzt. 1971 Sep;22(9):397-409.
7
[Uncombable hair syndrome].[难梳头发综合征]
Med Cutan Ibero Lat Am. 1977;5(1):39-46.
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[Netherton's syndrome in two sisters].
Ned Tijdschr Geneeskd. 2002 Jun 8;146(23):1087-90.
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Adrenoleucodystrophy: dermatological findings and skin surface lipid study.肾上腺脑白质营养不良:皮肤表现及皮肤表面脂质研究
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10
Netherton's syndrome: the importance of eyebrow hair.Netherton综合征:眉毛的重要性。
Dermatol Online J. 2007 Jul 13;13(3):21.

引用本文的文献

1
A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.一个新的角蛋白丝聚集素基因致病性变异导致弥漫性炎症性剥脱性皮肤综合征伴显著嗜酸性粒细胞增多和发内卷曲。
Pediatr Dermatol. 2022 Mar;39(2):268-272. doi: 10.1111/pde.14939. Epub 2022 Feb 17.
2
Pili Torti: A Feature of Numerous Congenital and Acquired Conditions.扭曲发:众多先天性和后天性疾病的一个特征。
J Clin Med. 2021 Aug 30;10(17):3901. doi: 10.3390/jcm10173901.