Chronic mucocutaneous candidiasis

被引:2
|
作者
Hon-Balla, Bernadett [1 ,2 ]
Erdos Melinda [3 ]
机构
[1] Semmelweis Egyet, Altalanos Orvostud Kar, Bor Nemikortani & Boronkol Klin, Budapest, Hungary
[2] Racz Karoly Klin Orvostud Doktori Iskola, Budapest, Hungary
[3] Semmelweis Egyet, Altalanos Orvostud Kar, Primer Immundeficientia Klin Reszleg & Lab, Bor Nemikortani & Boronkol Klin, Budapest, Hungary
关键词
chronic mucocutaneous candidiasis; Th17-cell; Candida; FUNCTION STAT1 MUTATIONS; DECTIN-1; DEFICIENCY; IL-17; IMMUNITY; INBORN-ERRORS; UNDERLIE; HUMANS; MYCOBACTERIAL; IMPAIRMENT; MECHANISMS; ALBICANS;
D O I
10.1556/650.2022.32409
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic mucocutaneous candidiasis is a genetically heterogeneous group of disorders, which are characterised by chronic or recurrent non-invasive skin, nail and mucous membrane infections caused by Candida. The increased susceptibility to Candida infections is due to a Th17-cell mediated immune detect with different gene mutations in the background. The isolated form of the disorder, referred to as chronic mucocutaneous candidiasis, presents primarily or only with mucocutaneous candidiasis. In contrast, the syndromic form of the disorder is characterised, besides the non-invasive Candida infections, by autoimmune disorders, which most commonly affect the endocrine system. Genetic tests are important in confirming the diagnosis, which in affected families would provide the opportunity for prenatal genetic testing. The authors present the main types of chronic mucocutaneous candidiasis, exploring the clinical aspects, diagnostic methods, and available therapies. Furthermore, the authors conclude the molecular genetic background and the currently known pathomechanism of the disorder.
引用
收藏
页码:171 / 180
页数:10
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