儿童肠病性肢端皮炎

Q3 Medicine
V. Novikova, A. A. Pokhlebkina, D. Zaslavsky, A. Khavkin
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引用次数: 0

摘要

肠病性肢端皮炎是一种罕见的遗传性锌缺乏症,其特征为周周和肢端皮炎、脱发和腹泻。指先天性锌代谢障碍,是一种常染色体隐性遗传病,由锌转运体SLC39A4基因突变引起。患病率为1至9:100万,新生儿总发病率为1:50万。这种疾病通常在婴儿时期表现出来,在停止母乳喂养并将婴儿换成牛奶配方奶粉的几周内,或者在出生后人工喂养的最初几天。肠病性肢端皮炎的典型临床表现为肢端及腰周皮炎、脱发和腹泻三位一体,但这三种症状同时出现的病例仅占20%。腹泻可与皮肤症状并发,可先于或后发生。皮肤病变的特征性征象包括在肘关节、膝关节、四肢远端、生殖器、腹股沟褶皱处出现界限分明、干燥、鳞状的红斑或水肿灶,伴有囊泡和脓疱,通常对称分布,边界清晰,轮廓不规则。皮肤综合征病程长,随着病程的发展,出现不愈合的糜烂和溃疡区。血浆锌缺乏症是诊断的金标准。大多数AE患儿血浆锌浓度低(<500 mcg/L或<50 mcg/dl),但空腹锌浓度低于70 mcg/L或年龄较大的非节食儿童锌浓度低于65 mcg/dl被认为具有诊断意义。这种疾病的治疗通常包括肠内或肠外给锌,剂量为1-3毫克/公斤/天。对于锌元素。5-10天内观察到临床反应。支持性锌治疗在患者的一生中都是必要的,尽管有缓解期的报道。局部治疗也可以使用:以乳霜形式的葡聚糖醇,每天3次涂抹在皮炎区域,可以增强再上皮化。没有明显的证据表明局部锌应用改善。肠病性肢端皮炎患者不需要活动限制。关键词:缺锌,肠性肢端皮炎,儿童
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enteropathic acrodermatitis in children
Enteropathic acrodermatitis is a rare hereditary form of zinc deficiency, characterized by periorial and acral dermatitis, alopecia and diarrhea. Refers to congenital disorders of zinc metabolism, inherited as an autosomal recessive disease resulting from mutations in the gene for the zinc transporter SLC39A4. The prevalence ranges from 1 to 9:1,000,000, with an overall incidence of 1:500,000 newborns. The disease usually manifests itself in infancy, within a few weeks of stopping breastfeeding and switching the baby to a cow's milk-based formula, or in the first days of life if artificially fed from birth. The classical clinical manifestations of acrodermatitis enteropathic are characterized by the triad: acral and periofital dermatitis, alopecia and diarrhea, but all three signs together occur only in 20% of cases. Diarrhea may develop concurrently with skin symptoms, may precede or occur later. Characteristic signs of skin lesions include sharply demarcated, dry, scaly erythematous plaques or edematous foci with vesicles and pustules on the skin of the elbow and knee joints, distal extremities, genitals, in the inguinal folds, which are usually symmetrically distributed, have sharp boundaries and irregular outlines. The course of the skin syndrome is long, as it progresses, non-healing erosive and ulcerative areas appear. Plasma zinc deficiency is the gold standard for diagnosis. Most infants with AE have low plasma zinc concentrations (<500 mcg/L or <50 mcg/dl), but a level of less than 70 mcg/L on an empty stomach or less than 65 mcg/dl in older non-dieting children is considered diagnostically significant. Treatment for this disease usually includes enteral or parenteral zinc administration, at a dose of 1-3 mg/kg/day. for elemental zinc. A clinical response is observed within 5–10 days. Supportive zinc therapy is necessary throughout the patient's life, although periods of remission have been reported. Topical therapy is also used: Dexpanthenol in the form of a cream, applied 3 times a day in the area of dermatitis, can enhance re-epithelialization. There is no significant evidence of improvement with topical zinc application. No activity restrictions are required for patients with acrodermatitis enteropathic. Key words: zinc deficiency, enteropathic acrodermatitis, children
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来源期刊
Voprosy Detskoi Dietologii
Voprosy Detskoi Dietologii Medicine-Pediatrics, Perinatology and Child Health
CiteScore
1.20
自引率
0.00%
发文量
17
期刊介绍: The scientific journal Voprosy Detskoi Dietologii is included in the Scopus database. Publisher country is RU. The main subject areas of published articles are Food Science, Pediatrics, Perinatology, and Child Health, Nutrition and Dietetics, Клиническая медицина.
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