肢皮炎enteropathica

María Elena Martínez-Bustamante , Rubén Peña-Vélez , Enory Almanza-Miranda , Carlos Andrés Aceves-Barrios , Tonatiuh Vargas-Pastrana , Alfredo Raúl Rodolfo Morayta-Ramírez Corona
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引用次数: 0

摘要

摘要肠病性肢端皮炎是一种低发病率疾病,由遗传性或后天缺锌引起。它的特点是肢端皮炎,脱发,腹泻和生长迟缓。皮肤病可以模拟皮肤真菌感染或其他病原体相关的皮肤病。病例报告我们报告一名7个月大的女性患者,因怀疑免疫缺陷和皮肤真菌病于11月20日被送往国家医学中心。她的病情开始时,皮肤病播散到头部、躯干和生殖器区域;最初给予抗真菌和广谱抗生素治疗,没有改善。入院后,免疫缺陷和真菌感染被丢弃。怀疑为肠病性肢端皮炎,后来经低血清锌水平证实。在口服锌治疗开始后,患者立即出现改善。结论肠病性肢端皮炎有多种鉴别诊断,包括皮肤感染。因此,早期识别特征性病变有利于怀疑、诊断和适当治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acrodermatitis enteropathica

Introduction

Acrodermatitis enteropathica is a low-incidence disease due to inherited or acquired zinc deficiency. It is characterized by acral dermatitis, alopecia, diarrhea and growth retardation. The dermatological condition may mimic a cutaneous fungal infection or other pathogen-related skin diseases.

Case report

We report the case of a female patient of 7 months of age, who was sent to Centro Médico Nacional 20 de Noviembre for suspicion of immunodeficiency and cutaneous mycosis. Her condition began with dermatosis disseminated to the head, trunk and genital region; initial treatment with antifungal and broad spectrum antibiotics was given, without improvement. Upon admission, immunodeficiency and fungal infection were discarded. Acrodermatitis enteropathica was suspected, and corroborated later by low serum zinc levels. Immediately after the start of oral treatment with zinc, the patient showed improvement.

Conclusions

There are multiple differential diagnoses of acrodermatitis enteropathica, which includes cutaneous infections. Therefore, the early recognition of the characteristic lesions favors suspicion, diagnosis and appropriate treatment.

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