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伴有抗核抗体阳性的罗斯综合征：提示可能的自身免疫起源及静脉注射免疫球蛋白治疗

Ross syndrome with ana positivity: a clue to possible autoimmune origin and treatment with intravenous immunoglobulin.

作者信息

Vasudevan Biju, Sawhney Mps, Vishal S

机构信息

Department of Dermatology and Venereology, Base Hospital, Delhi Cantt, India.

出版信息

Indian J Dermatol. 2010 Jul-Sep;55(3):274-6. doi: 10.4103/0019-5154.70694.

DOI:10.4103/0019-5154.70694
PMID:21063524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2965918/
Abstract

A 28-year-old serving soldier presented with patchy areas of absence of sweating and blurring of vision. On examination he was found to have segmental anhidrosis, right sided tonic pupil and absent ankle jerks. Investigations revealed ANA positivity with no other abnormalities. He was treated with Intravenous immunoglobulin. This case of Ross syndrome is reported for its rarity as well as a clue to its probable autoimmune origin and treatment option with intravenous immunoglobulins.

摘要

一名28岁的现役军人出现了片状无汗区域和视力模糊的症状。检查发现他有节段性无汗、右侧强直性瞳孔和跟腱反射消失。检查显示抗核抗体阳性，无其他异常。他接受了静脉注射免疫球蛋白治疗。报道这例罗斯综合征是因其罕见，以及提示其可能的自身免疫起源和静脉注射免疫球蛋白的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/31e76164cc48/IJD-55-274-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/75104488d09d/IJD-55-274-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/7ffbfa787007/IJD-55-274-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/61317e32f8e4/IJD-55-274-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/7373d4d71a8c/IJD-55-274-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/31e76164cc48/IJD-55-274-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/75104488d09d/IJD-55-274-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/7ffbfa787007/IJD-55-274-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/61317e32f8e4/IJD-55-274-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/7373d4d71a8c/IJD-55-274-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2daa/2965918/31e76164cc48/IJD-55-274-g005.jpg

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本文引用的文献

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2
Holmes-Adie syndrome, autoimmune hepatitis and celiac disease: a case report.霍姆斯-阿迪综合征、自身免疫性肝炎与乳糜泻：一例报告
World J Gastroenterol. 2006 Mar 7;12(9):1485-7. doi: 10.3748/wjg.v12.i9.1485.
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Holmes-Adie syndrome with segmental hypohidrosis.伴有节段性少汗的霍姆斯-阿迪综合征。
Cureus. 2022 Feb 16;14(2):e22305. doi: 10.7759/cureus.22305. eCollection 2022 Feb.
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Clinical presentation and autonomic profile in Ross syndrome.罗斯综合征的临床表现及自主神经特征
J Neurol. 2021 Oct;268(10):3852-3860. doi: 10.1007/s00415-021-10531-8. Epub 2021 Apr 3.
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A case of Ross syndrome associated with systemic sclerosis.一例与系统性硬化症相关的罗斯综合征病例。
Clin Auton Res. 2021 Jun;31(3):463-465. doi: 10.1007/s10286-021-00773-x. Epub 2021 Feb 4.
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Is Ross Syndrome a New Type of Synucleinopathy? A Brief Research Report.罗斯综合征是一种新型突触核蛋白病吗？一篇简短的研究报告。
Front Neurosci. 2020 Jul 8;14:635. doi: 10.3389/fnins.2020.00635. eCollection 2020.
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Ross Syndrome.罗斯综合征
Neuroophthalmology. 2019 Dec 12;44(3):201-203. doi: 10.1080/01658107.2019.1669184. eCollection 2020 Jun.
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J Family Med Prim Care. 2019 Apr;8(4):1500-1503. doi: 10.4103/jfmpc.jfmpc_151_19.
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Indian J Dermatol. 2016 May-Jun;61(3):348. doi: 10.4103/0019-5154.182472.
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A lady presenting with segmental anhidrosis and heat intolerance.一位表现为节段性无汗和不耐热的女性。
Indian Dermatol Online J. 2015 Mar-Apr;6(2):126-7. doi: 10.4103/2229-5178.153019.
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Idiopathic autonomic neuropathy: comparison of cases seropositive and seronegative for ganglionic acetylcholine receptor antibody.特发性自主神经病变：神经节乙酰胆碱受体抗体血清阳性与血清阴性病例的比较
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