Suppr超能文献

婴儿系统性透明变性:免疫系统细胞和体液分支受损导致感染的病例报告

Infantile Systemic Hyalinosis: A Case Report of Compromised Cellular and Humoral Branches of the Immune System Leading to Infections.

作者信息

Klebanova Yana, Schwindt Christina

机构信息

Department of Pediatrics, University of California, Irvine, Orange, California.

出版信息

Pediatr Asthma Allergy Immunol. 2009 Sep;22(3):127-130. doi: 10.1089/pai.2009.0011.

Abstract

Infantile systemic hyalinosis (ISH) is a rare disorder characterized by hyaline deposition in the skin as well as visceral organs. Though commonly associated with a protein losing enteropathy (PLE) and loss of immunoglobulins the profile of cellular and humoral branches of the immune system has not previously been described. We describe the immune system deficits in a case of ISH associated with PLE and infections. A history of multiple infections prompted an immunocompetency evaluation in a patient with ISH and PLE. Low immunoglobulin G (IgG), poorly protective pneumococcal titers, and nonresponse to Candida on lymphocyte transformation in the face of increasing infections lead to the diagnosis of a combined immunodeficiency. This is the first case report detailing quantitative and qualitative deficits of the humoral and cellular branches of the immune system in a patient with ISH. The understanding of the different aspects of this disease including the immune deficits impacts not only prognosis but also end-of-life decisions as well.

摘要

婴儿系统性透明变性(ISH)是一种罕见的疾病,其特征是在皮肤以及内脏器官中出现透明质沉积。尽管通常与蛋白丢失性肠病(PLE)和免疫球蛋白丢失有关,但此前尚未描述免疫系统的细胞和体液分支情况。我们描述了一例与PLE和感染相关的ISH患者的免疫系统缺陷。多次感染史促使对一名患有ISH和PLE的患者进行免疫功能评估。免疫球蛋白G(IgG)水平低、肺炎球菌滴度保护性差以及面对不断增加的感染时淋巴细胞转化对念珠菌无反应,导致诊断为联合免疫缺陷。这是第一例详细描述ISH患者免疫系统体液和细胞分支定量和定性缺陷的病例报告。对这种疾病不同方面的理解,包括免疫缺陷,不仅影响预后,也影响临终决策。

相似文献

2
Infantile systemic hyalinosis: a case report with a novel mutation.
Oman Med J. 2013 Jan;28(1):53-5. doi: 10.5001/omj.2013.12.
3
Infantile Systemic Hyalinosis: A Case Report and Literature Review.
Cureus. 2023 Oct 5;15(10):e46519. doi: 10.7759/cureus.46519. eCollection 2023 Oct.
4
Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis-A Case Report.
J Oral Maxillofac Surg. 2015 Oct;73(10):1962.e1-5. doi: 10.1016/j.joms.2015.06.176. Epub 2015 Jul 8.
5
[Infantile systemic hyalinosis: a case report and literature review].
Zhonghua Er Ke Za Zhi. 2016 Dec 2;54(12):946-949. doi: 10.3760/cma.j.issn.0578-1310.2016.12.015.
6
Protein-losing enteropathy and joint contractures caused by a novel homozygous ANTXR2 mutation.
Adv Genomics Genet. 2018;8:17-21. doi: 10.2147/AGG.S159077. Epub 2018 Jun 27.
7
Infantile systemic hyalinosis: Case report and review of the literature.
J Am Acad Dermatol. 2008 Feb;58(2):303-7. doi: 10.1016/j.jaad.2007.06.008.
8
Hyaline Fibromatosis Syndrome: A Rare Inherited Disorder.
Indian J Dermatol. 2016 Sep-Oct;61(5):580. doi: 10.4103/0019-5154.190129.
10
Infantile Systemic Hyalinosis: Report of 17-year Experience.
Iran J Pediatr. 2014 Dec;24(6):775-8. Epub 2014 Dec 9.

引用本文的文献

本文引用的文献

1
Infantile systemic hyalinosis: report of three Iranian children and review of the literature.
Clin Rheumatol. 2007 Jan;26(1):128-30. doi: 10.1007/s10067-005-0124-y. Epub 2005 Dec 3.
2
Infantile systemic hyalinosis: a clinicopathological study.
Am J Med Genet A. 2004 Sep 1;129A(3):282-5. doi: 10.1002/ajmg.a.30117.
3
Infantile systemic hyalinosis.
J Am Acad Dermatol. 2004 Feb;50(2 Suppl):S61-4. doi: 10.1016/s0190-9622(03)02798-1.
4
Infantile systemic hyalinosis.
J Craniofac Surg. 2003 Sep;14(5):719-23. doi: 10.1097/00001665-200309000-00022.
5
Immunologic profile of patients with protein-losing enteropathy complicating congenital heart disease.
Pediatr Cardiol. 2002 Nov-Dec;23(6):587-93. doi: 10.1007/s00246-001-0078-z.

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