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大疱性表皮松解症的耳鼻咽喉及食管表现

Otorhinolaryngological and esophageal manifestations of epidermolysis bullosa.

作者信息

Fantauzzi Rodrigo Santana, Maia Mariana Oliveira, Cunha Flávia Coelho, Simões Rodrigo Vidal, Gonçalves Denise Utsch, Maia Amélio Ferreira

机构信息

Otorhinolaryngologist, Member of the Clinical Team at Hospital Municipal de Contagem.

MD, Resident at the ENT Service at Hospital das Clínicas da UFMG.

出版信息

Braz J Otorhinolaryngol. 2008 Sep-Oct;74(5):657-661. doi: 10.1016/S1808-8694(15)31373-2.

Abstract

UNLABELLED

Epidermolysis bullosa (EB) is a group of skin diseases with different clinical manifestations and varied inheritance patterns. Blisters may appear spontaneously or following minimal trauma to the skin or mucosa.

AIM

this paper aims to describe the otorhinolaryngological manifestations and esophageal complications related to EB, and the experience in treating patients with esophageal stenosis secondary to this disease.

MATERIALS AND METHOD

this descriptive study enrolled 60 patients with EB seen from June 1999 to December 2006 at the Head and Neck Surgery Service of X Hospital, a reference center for EB.

RESULTS

the patients' mean age was 14.5 years. Twenty-eight (46.6%) were females and 32 (53.4%) were males. Eight (13.4%) were diagnosed with epidermolysis bullosa simplex, while 51 (85%) had epidermolysis bullosa dystrophica; one (1.6%) patient had one acquired EB. Lips, mouth, tongue and ears were the most frequently involved sites (32 patients - 53.3%). Dysphagia was found in 28 patients (46.6%). After esophageal dilatation the symptoms subsided.

CONCLUSION

EB is a rare disease and patients must be sent for treatment at reference centers. Physicians treating patients for EB must be aware of the measures required to improve the quality of the treatment provided without putting the patients in harm's way.

摘要

未标注

大疱性表皮松解症(EB)是一组临床表现各异、遗传方式多样的皮肤病。水疱可自发出现,或在皮肤或黏膜受到轻微创伤后出现。

目的

本文旨在描述与EB相关的耳鼻咽喉科表现和食管并发症,以及治疗该疾病继发食管狭窄患者的经验。

材料与方法

这项描述性研究纳入了1999年6月至2006年12月在X医院头颈外科就诊的60例EB患者,该医院是EB的参考中心。

结果

患者的平均年龄为14.5岁。28例(46.6%)为女性,32例(53.4%)为男性。8例(13.4%)被诊断为单纯性大疱性表皮松解症,51例(85%)患有营养不良性大疱性表皮松解症;1例(1.6%)患者患有获得性EB。嘴唇、口腔、舌头和耳朵是最常受累的部位(32例患者 - 53.3%)。28例患者(46.6%)出现吞咽困难。食管扩张后症状缓解。

结论

EB是一种罕见疾病,患者必须转诊至参考中心进行治疗。治疗EB患者的医生必须了解在不伤害患者的情况下提高治疗质量所需的措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc6e/9445973/1f5b36ca5723/gr1.jpg

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