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慢性萎缩性肢端皮炎:莱姆病晚期的多种表现形式。

Acrodermatitis chronica atrophicans: various faces of the late form of Lyme borreliosis.

作者信息

Moniuszko-Malinowska Anna, Czupryna Piotr, Dunaj Justyna, Pancewicz Sławomir, Garkowski Adam, Kondrusik Maciej, Grygorczuk Sambor, Zajkowska Joanna

机构信息

Department of Infectious Diseases and Neuroinfections, Medical University of Białystok, Białystok, Poland.

出版信息

Postepy Dermatol Alergol. 2018 Oct;35(5):490-494. doi: 10.5114/ada.2018.77240. Epub 2018 Jul 19.

Abstract

INTRODUCTION

Acrodermatitis chronica atrophicans (ACA) is probably the most common late and chronic manifestation of the Lyme borreliosis seen in European patients.

AIM

To analyze epidemiological data, and to investigate the effects of treatment of patients with ACA.

MATERIAL AND METHODS

Nine patients were included in the study. All patients had serological examinations (ELISA and Western blot) and histopathological examination of the skin lesions performed. Eight patients had PCR in the skin biopsy performed.

RESULTS

The duration of symptoms ranged from 2 months to 2 years. In 7 patients, skin lesions were located on lower limbs, in 2 patients - in a non-typical body area - abdomen. In 1 patient, scleroderma and in 3 patients, diabetes mellitus was diagnosed. DNA was detected in 25% of the skin biopsy specimens. IgG anti- specific antibodies were present in serum of all patients (confirmed by Western blot). In all cases, the diagnosis was confirmed by histopathological examination. The response to ceftriaxone therapy varied. In 5 cases, the lesions resolved completely, in others they faded.

CONCLUSIONS

Despite raising awareness of Lyme borreliosis, late forms of the disease such as ACA are still observed. Acrodermatitis chronica atrophicans skin lesions may be located in non-characteristic areas, e.g. abdominal skin. Symptoms are not irritating or painful, therefore patients do not seek medical help. The effect of antibiotic treatment varies.

摘要

引言

慢性萎缩性肢端皮炎(ACA)可能是欧洲患者中莱姆病最常见的晚期慢性表现。

目的

分析流行病学数据,并研究ACA患者的治疗效果。

材料与方法

9名患者纳入本研究。所有患者均进行了血清学检查(酶联免疫吸附测定和免疫印迹法)以及皮肤病变的组织病理学检查。8名患者进行了皮肤活检的聚合酶链反应。

结果

症状持续时间为2个月至2年。7名患者的皮肤病变位于下肢,2名患者位于非典型身体部位——腹部。1名患者被诊断为硬皮病,3名患者被诊断为糖尿病。25%的皮肤活检标本中检测到DNA。所有患者血清中均存在IgG抗特异性抗体(经免疫印迹法确认)。所有病例均通过组织病理学检查确诊。头孢曲松治疗的反应各不相同。5例病变完全消退,其他病例病变变淡。

结论

尽管人们对莱姆病的认识有所提高,但仍观察到该疾病的晚期形式,如ACA。慢性萎缩性肢端皮炎的皮肤病变可能位于非特征性区域,如腹部皮肤。症状不具有刺激性或疼痛性,因此患者不会寻求医疗帮助。抗生素治疗的效果各不相同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f10/6232541/77e8a3e2424d/PDIA-35-77240-g001.jpg

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