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老年女性迟发性播散性浅表性光化性汗孔角化症。

Late-onset disseminated superficial actinic porokeratosis in an elderly woman.

机构信息

Department of Dermatology, Charles Nicolle Hospital, Boulevard 9 Avril Tunis, Tunis, Tunisia 1006.

出版信息

Dermatol Ther (Heidelb). 2011 Sep;1(1):15-9. doi: 10.1007/s13555-011-0004-0. Epub 2011 May 20.

DOI:10.1007/s13555-011-0004-0
PMID:22984659
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3437640/
Abstract

INTRODUCTION

Disseminated superficial actinic porokeratosis (DSAP) is the most common form of porokeratosis. A case of late-onset DSAP is reported with an uncommon presentation in an elderly patient.

METHODS

An 80-year-old woman, with diabetes mellitus treated with metformin, and hypertension treated with metoprolol and captopril, presented with multiple 2 mm-to-7 cm brown patches, for 5 years. The patches were often confluent with an atrophic center and a well-demarcated keratotic border located on the thighs, lower legs, and feet.

RESULTS

Histological examination of a cutaneous biopsy showed the presence of rare cornoid lamellae, confirming the clinical diagnosis of DSAP.

CONCLUSION

In this report, the atypical presentation of DSAP is discussed in this elderly patient and also the possible triggering factors at this age.

摘要

简介

播散性浅表性光线性汗孔角化症(DSAP)是汗孔角化症中最常见的一种类型。本文报道了一例罕见的迟发性 DSAP 病例,其在老年患者中表现为不常见的临床表现。

方法

一位 80 岁的女性,患有糖尿病,接受二甲双胍治疗,患有高血压,接受美托洛尔和卡托普利治疗,出现多发性 2 毫米至 7 厘米的棕色斑块,持续 5 年。这些斑块经常融合,具有萎缩中心和位于大腿、小腿和足部的边界清楚的角化边界。

结果

皮肤活检的组织学检查显示罕见的Cornoid 板层存在,证实了 DSAP 的临床诊断。

结论

在本报告中,讨论了这位老年患者中 DSAP 的非典型表现以及这个年龄可能的触发因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/15509d9fa3c9/13555_2011_4_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/8b58c44d41ad/13555_2011_4_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/409c6d7c81af/13555_2011_4_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/a7deabdf3528/13555_2011_4_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/15509d9fa3c9/13555_2011_4_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/8b58c44d41ad/13555_2011_4_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/409c6d7c81af/13555_2011_4_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/a7deabdf3528/13555_2011_4_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d9e/3721529/15509d9fa3c9/13555_2011_4_Fig4_HTML.jpg

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本文引用的文献

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J Dermatolog Treat. 2012 Feb;23(1):52-6. doi: 10.3109/09546634.2010.495381. Epub 2010 Oct 22.
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Atypical porokeratosis developing following bone marrow transplantation in a patient with myelodysplastic syndrome.骨髓增生异常综合征患者骨髓移植后发生的非典型汗孔角化症。
Ann Dermatol. 2010 May;22(2):206-8. doi: 10.5021/ad.2010.22.2.206. Epub 2010 May 18.
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Disseminated superficial actinic porokeratosis co-existing with linear and verrucous porokeratosis in an elderly woman: Update on the genetics and clinical expression of porokeratosis.
老年女性并发播散性浅表性光化性汗孔角化症、线状和疣状汗孔角化症:汗孔角化症的遗传学和临床表现更新。
J Am Acad Dermatol. 2010 Nov;63(5):886-91. doi: 10.1016/j.jaad.2009.07.038. Epub 2010 May 6.
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Development of segmental superficial actinic porokeratosis during immunosuppressive therapy for pemphigus vulgaris.寻常型天疱疮免疫抑制治疗期间节段性浅表光化性汗孔角化症的发生
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