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[一例罕见的与自身免疫性多内分泌腺病、念珠菌病和外胚层营养不良(APECED)相关的青少年糖尿病,具有强烈的X连锁家族遗传]

[A rare case of juvenile diabetes mellitus associated with APECED (autoimmune poly-endocrinopathy, candidiasis and ectodermal dystrophy) with strong X-linked familial inheritance].

作者信息

Iannello S, Campanile E, Cipolli D, Gallina M, Merola A, Puglisi S, Tabita V, Belfiore F

机构信息

Cattedra di Medicina Interna, Ospedale Garibaldi, Calania.

出版信息

Minerva Endocrinol. 1997 Jun;22(2):51-9.

PMID:9304048
Abstract

The polyglandular autoimmune syndromes (PGA) are well known and are distinguished into type I, type II and type III. PGAI, also called APECED (autoimmune polyendocrinopathy, candidiasis and ectodermal dystrophy), is an autosomal recessive disorder, appearing in childhood and typically characterized by hypoparathyroidism (unusual in PGAII and PGAIII) and adrenal insufficiency. In APECED, autoimmune destruction of the pancreatic beta cells with development of insulin-dependent type 1 diabetes is possible, but less frequent than in the other PGAs, especially PGAII. The pathogenesis of this unique autoimmune disease is unknown. No HLA association seems to exist and genetic studies have assigned the autosomal APECED locus to chromosome 21. The case of a 28-years-old female suggesting the diagnosis of APECED, is presented, characterized by psycho-somatic abnormal development, teeth alterations, post-puberal gonadal failure with dystrophic hypoplasia of external genitalia, previous vaginal candidiasis, a slowly developing juvenile brittle diabetes. Intestinal malabsorption induced by Giardia lamblia occurred (probably resulting, like candidiasis, from immunological anergy). A strong familiarity linked to female sex was noticed (the mother, a sister, the little nice and some maternal female cousins being affected) while the father and a brother were healthy. Diabetes seems to be characterized by early onset and severe complications. In this patient no organo-specific antibodies were detected and the only immunologic disorder was a small decrease of CD3 and CD4/CD8 ratio, both CD4 and CD8 being at the lower normal range. This patient (and her female maternal relatives) needs a long-term follow-up in order to evaluate the function of endocrine glands and to initiate early treatment for hormonal deficits, as well as to detect the non-endocrine components of disease.

摘要

多腺体自身免疫综合征(PGA)广为人知,分为I型、II型和III型。I型PGA,也称为自身免疫性多内分泌病、念珠菌病和外胚层营养不良(APECED),是一种常染色体隐性疾病,出现在儿童期,典型特征为甲状旁腺功能减退(在II型和III型PGA中不常见)和肾上腺功能不全。在APECED中,胰腺β细胞可能会发生自身免疫性破坏并发展为胰岛素依赖型1型糖尿病,但比其他PGA,尤其是II型PGA的发生率要低。这种独特的自身免疫性疾病的发病机制尚不清楚。似乎不存在HLA关联,基因研究已将常染色体APECED基因座定位于21号染色体。本文介绍了一名28岁女性疑似APECED的病例,其特征为身心发育异常、牙齿改变、青春期后性腺功能衰竭伴外生殖器营养不良性发育不全、既往有阴道念珠菌病、缓慢发展的青少年脆性糖尿病。发生了由蓝氏贾第鞭毛虫引起的肠道吸收不良(可能与念珠菌病一样,是由免疫无反应性导致)。注意到与女性性别有很强的家族关联性(母亲、一个姐妹、小侄女和一些母系女性表亲患病),而父亲和一个兄弟健康。糖尿病似乎具有发病早和并发症严重的特点。在该患者中未检测到器官特异性抗体,唯一的免疫紊乱是CD3及CD4/CD8比值略有下降,CD4和CD8均处于正常范围下限。该患者(及其母系女性亲属)需要长期随访,以评估内分泌腺功能,并针对激素缺乏症尽早开始治疗,同时检测疾病的非内分泌成分。

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