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一名患有斯内登综合征的8岁儿童：罕见病例报告。

An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report.

作者信息

Nallur Siddaraju Maheshwari, Samynathan Archana, Kurakula Sowjanya, Kharge Priyadarshini, Nalla Sanjana D

机构信息

Dermatology, Bangalore Medical College and Research Institute, Bangalore, IND.

Dermatology, George Washington University, Virginia, USA.

出版信息

Cureus. 2023 Jun 6;15(6):e40054. doi: 10.7759/cureus.40054. eCollection 2023 Jun.

DOI:10.7759/cureus.40054
PMID:37425554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10325693/
Abstract

We present a rare case of slow-progressing neurocutaneous vasculopathy described as Sneddon syndrome. A child presented with global developmental delay, congenital livedo racemosa, unilateral vision loss, and a past history of focal neurological deficit. Our main objective is to make physicians aware of this nature of presentation in children.

摘要

我们报告了一例罕见的进展缓慢的神经皮肤血管病变，称为斯内登综合征。一名儿童出现全面发育迟缓、先天性网状青斑、单眼视力丧失，以及既往有局灶性神经功能缺损病史。我们的主要目的是让医生了解儿童这种表现的性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/10325693/978a8559d6f7/cureus-0015-00000040054-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/10325693/2946129bf824/cureus-0015-00000040054-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/10325693/7ba0b2706a37/cureus-0015-00000040054-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/10325693/978a8559d6f7/cureus-0015-00000040054-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/10325693/2946129bf824/cureus-0015-00000040054-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/10325693/7ba0b2706a37/cureus-0015-00000040054-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66d0/10325693/978a8559d6f7/cureus-0015-00000040054-i03.jpg

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引用本文的文献

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本文引用的文献

1
Sneddon syndrome: a comprehensive clinical review of 53 patients.斯奈德综合征：53 例患者的综合临床回顾。
J Neurol. 2021 Jul;268(7):2450-2457. doi: 10.1007/s00415-021-10407-x. Epub 2021 Jan 29.
2
Sneddon syndrome.斯内登综合征
Pan Afr Med J. 2019 Sep 4;34:9. doi: 10.11604/pamj.2019.34.9.11903. eCollection 2019.
3
Sneddon Syndrome: A Comprehensive Overview.斯内登综合征：全面概述。
J Stroke Cerebrovasc Dis. 2019 Aug;28(8):2098-2108. doi: 10.1016/j.jstrokecerebrovasdis.2019.05.013. Epub 2019 May 31.
4
Long-term follow-up of early-onset Sneddon syndrome: A case report.早发性斯内登综合征的长期随访：一例报告
JAAD Case Rep. 2018 Oct 3;4(9):880-882. doi: 10.1016/j.jdcr.2018.08.008. eCollection 2018 Oct.
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Sneddon's syndrome: a comprehensive review of the literature.斯内登综合征：文献综述
Orphanet J Rare Dis. 2014 Dec 31;9:215. doi: 10.1186/s13023-014-0215-4.
6
Improvement of neurological symptoms and memory and emotional status in a case of seronegative Sneddon syndrome with cyclophosphamide.环磷酰胺治疗血清阴性Sneddon综合征1例，神经症状、记忆及情绪状态改善
Clin Neurol Neurosurg. 2010 Jul;112(6):544-7. doi: 10.1016/j.clineuro.2010.04.002. Epub 2010 May 4.
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Advances in the genetics of cerebrovascular disease and stroke.脑血管疾病与中风遗传学的进展
Neurology. 2001 Apr 24;56(8):997-1008. doi: 10.1212/wnl.56.8.997.
8
Sneddon syndrome with or without antiphospholipid antibodies. A comparative study in 46 patients.伴或不伴抗磷脂抗体的斯内登综合征。46例患者的对比研究。
Medicine (Baltimore). 1999 Jul;78(4):209-19. doi: 10.1097/00005792-199907000-00001.
9
Nevus comedonicus syndrome: a new pediatric case.黑头粉刺痣综合征：一例新的儿科病例。
Pediatr Dermatol. 1998 Jul-Aug;15(4):304-6. doi: 10.1046/j.1525-1470.1998.1998015304.x.
10
Sneddon's syndrome. A long-term follow-up of 21 patients.斯内登综合征。21例患者的长期随访
Arch Dermatol. 1993 Apr;129(4):437-47. doi: 10.1001/archderm.129.4.437.