Suppr超能文献

一名16岁菲律宾女孩的皮肤异色性淀粉样变:病例报告

Amyloidosis Cutis Dyschromica in a 16-Year-Old Filipino Girl: A Case Report.

作者信息

Bautista Fendi Ej R, Marte-Jimenez Marcia Marie S, Jamora Maria Jasmin J

机构信息

Skin and Cancer Foundation Incorporated, Pasig City 1605, Philippines.

出版信息

Dermatopathology (Basel). 2022 Dec 29;10(1):20-24. doi: 10.3390/dermatopathology10010002.

Abstract

Amyloidosis cutis dyschromica is a rare variant of primary cutaneous amyloidosis characterized by hyper- and hypopigmented macules. In this paper, we reported a case of a 16-year-old Filipino girl with hyper- and hypopigmented to depigmented macules on the upper and lower extremities, which started when she was 9 years of age.

摘要

皮肤异色性淀粉样变是原发性皮肤淀粉样变的一种罕见变异型,其特征为色素沉着过多和过少的斑疹。在本文中,我们报告了一例16岁菲律宾女孩的病例,她的上肢和下肢出现色素沉着过多、过少至色素脱失的斑疹,这些斑疹在她9岁时开始出现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aba6/9844270/50db5a791e21/dermatopathology-10-00002-g001.jpg

相似文献

1
Amyloidosis Cutis Dyschromica in a 16-Year-Old Filipino Girl: A Case Report.
Dermatopathology (Basel). 2022 Dec 29;10(1):20-24. doi: 10.3390/dermatopathology10010002.
2
Amyloidosis cutis dyschromica.
Orphanet J Rare Dis. 2012 Dec 12;7:95. doi: 10.1186/1750-1172-7-95.
3
Association of amyloidosis cutis dyschromica and familial Mediterranean fever.
An Bras Dermatol. 2017;92(5 Suppl 1):21-23. doi: 10.1590/abd1806-4841.20176114.
4
Amyloidosis Cutis Dyschromica: A Rare Reticulate Pigmentary Dermatosis.
Indian J Dermatol. 2015 Jul-Aug;60(4):385-7. doi: 10.4103/0019-5154.160491.
5
Late-onset amyloidosis cutis dyschromica: an unusual case.
Dermatol Online J. 2019 Apr 15;25(4):13030/qt07s4p19h.
7
Amyloidosis cutis dyschromica in two female siblings: cases report.
BMC Dermatol. 2011 Feb 15;11:4. doi: 10.1186/1471-5945-11-4.
8
Amyloidosis cutis dyschromica.
Indian Dermatol Online J. 2013 Oct;4(4):344-6. doi: 10.4103/2229-5178.120678.
9
Dermoscopy of Amyloidosis Cutis Dyschromica.
Indian J Dermatol. 2024 May-Jun;69(3):282. doi: 10.4103/ijd.ijd_934_23. Epub 2024 Jun 26.
10
Amyloidosis cutis dyschromica: a rare pigmentary disorder.
J Cutan Pathol. 2011 Oct;38(10):823-6. doi: 10.1111/j.1600-0560.2011.01701.x. Epub 2011 May 19.

本文引用的文献

2
Amyloidosis Cutis Dyschromica, A Rare Subtype of Primary Cutaneous Amyloidosis: Case Report and Literature Review.
Indian Dermatol Online J. 2021 Mar 2;12(2):330-334. doi: 10.4103/idoj.IDOJ_293_20. eCollection 2021 Mar-Apr.
3
Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica.
J Invest Dermatol. 2019 Dec;139(12):2550-2554.e9. doi: 10.1016/j.jid.2019.05.021. Epub 2019 Jun 19.
4
Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.
Am J Hum Genet. 2018 Feb 1;102(2):219-232. doi: 10.1016/j.ajhg.2017.12.012. Epub 2018 Jan 11.
5
Amyloidosis cutis dyschromica in two siblings and review of the epidemiology, clinical features and management in 48 cases.
Australas J Dermatol. 2016 Nov;57(4):307-311. doi: 10.1111/ajd.12342. Epub 2015 Apr 12.
7
Amyloidosis cutis dyschromica.
Indian Dermatol Online J. 2013 Oct;4(4):344-6. doi: 10.4103/2229-5178.120678.
8
Amyloidosis cutis dyschromica.
Orphanet J Rare Dis. 2012 Dec 12;7:95. doi: 10.1186/1750-1172-7-95.
9
Amyloidosis cutis dyschromica. DNA repair reduction in the cellular response to UV light.
Arch Dermatol. 1992 Jul;128(7):966-70. doi: 10.1001/archderm.128.7.966.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验