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[营养不良性隐性大疱性表皮松解症的消化系统受累。附6例报告并文献复习]

[Digestive involvement in dystrophic recessive epidermolysis bullosa. Apropos of 6 cases and review of the literature].

作者信息

Fortier-Beaulieu M, Teillac D, de Prost Y

机构信息

Unité de Dermatologie, Hôpital Necker-Enfants Malades, Paris.

出版信息

Ann Dermatol Venereol. 1987;114(8):963-71.

PMID:3322146
Abstract

Six personal cases of digestive tract involvement in dystrophic recessive epidermolysis bullosa are reported, and the relevant literature is reviewed. The study deals with the clinical aspects of these cases (buccal and dental lesions, digestive symptoms, effects on nutritional status; table I), as well as with their biochemical (table II), radiological and endoscopic aspects (table III, fig. 1 and 2). All patients presented with bucco-dental lesions, including two cases of congenital abnormalities: one with malposition and dysgenesis of the teeth, the other with dysplasia of the enamel in a patient whose dystrophic skin disease was proven by electron microscopic study. The oesophagus was involved in six cases, with tight concentric stenosis (2 cases), retrocricoidal stenosis (1 case) and oesophagitis (2 cases). No gastro-duodenal or intestinal lesions were detected. A case of constipation was related to anal involvement. The patients' nutritional status was investigated clinically and biochemically. A search for intestinal malabsorption by means of specific tests was conducted in 2 patients and proved negative. A study of the literature provided data on the nature and specificity of dental lesions. The morphological features, complications and physiopathology of oesophageal stenoses are described The existence of gastrointestinal lesions is discussed. Nutritional repercussions are presented and their causes are discussed. Attention is paid to the medical and surgical treatments of these lesions.

摘要

报告了6例营养不良性隐性大疱性表皮松解症累及消化道的病例,并对相关文献进行了综述。该研究涉及这些病例的临床方面(口腔和牙齿病变、消化症状、对营养状况的影响;表I),以及生化方面(表II)、放射学和内镜方面(表III,图1和图2)。所有患者均有口腔牙齿病变,包括2例先天性异常:1例牙齿错位和发育不全,另1例釉质发育异常,该患者的营养不良性皮肤病经电子显微镜检查证实。6例患者食管受累,表现为紧密的同心性狭窄(2例)、环状软骨后狭窄(1例)和食管炎(2例)。未检测到胃十二指肠或肠道病变。1例便秘与肛门受累有关。对患者的营养状况进行了临床和生化调查。对2例患者进行了特定试验以寻找肠道吸收不良,结果为阴性。对文献的研究提供了有关牙齿病变性质和特异性的数据。描述了食管狭窄的形态特征、并发症和病理生理学。讨论了胃肠道病变的存在情况。介绍了营养方面的影响并讨论了其原因。关注了这些病变的内科和外科治疗。

相似文献

1
[Digestive involvement in dystrophic recessive epidermolysis bullosa. Apropos of 6 cases and review of the literature].[营养不良性隐性大疱性表皮松解症的消化系统受累。附6例报告并文献复习]
Ann Dermatol Venereol. 1987;114(8):963-71.
2
Gastrointestinal manifestations of epidermolysis bullosa in children.儿童大疱性表皮松解症的胃肠道表现
Arch Dermatol. 1988 May;124(5):746-52.
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[Gastrointestinal manifestations of recessive dystrophic epidermolysis bullosa].[隐性营养不良型大疱性表皮松解症的胃肠道表现]
Bol Med Hosp Infant Mex. 1990 Jan;47(1):20-5.
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Hereditary epidermolysis bullosa. Dental management of three cases.遗传性大疱性表皮松解症。三例病例的牙科治疗
Med Oral. 2001 Jan-Feb;6(1):48-56.
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[Syndromes 13. Epidermolysis bullosa].[综合征13. 大疱性表皮松解症]
Ned Tijdschr Tandheelkd. 1999 Aug;106(8):302-5.
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Dental caries risk in hereditary epidermolysis bullosa.遗传性大疱性表皮松解症中的龋齿风险
Pediatr Dent. 1994 Nov-Dec;16(6):427-32.
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Gastrointestinal complications of inherited epidermolysis bullosa: cumulative experience of the National Epidermolysis Bullosa Registry.遗传性大疱性表皮松解症的胃肠道并发症:国家大疱性表皮松解症登记处的累积经验
J Pediatr Gastroenterol Nutr. 2008 Feb;46(2):147-58. doi: 10.1097/MPG.0b013e31812f5667.
8
Dermolytic (dystrophic) epidermolysis bullosa inversa.溶解性(营养不良性)反向大疱性表皮松解症。
Arch Dermatol. 1988 Apr;124(4):544-7.
9
[Therapy of esophageal stenoses in recessive epidermolysis bullosa dystrophica].[隐性营养不良性大疱性表皮松解症食管狭窄的治疗]
Laryngol Rhinol Otol (Stuttg). 1985 Oct;64(10):522-6.
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[Surgical treatment of esophageal stenosis with recessive dystrophic epidermolysis bullosa--esophageal dilatation using balloon catheter method].
Nihon Hifuka Gakkai Zasshi. 1989 Feb;99(2):141-7.