Marks J G, Belsito D V, DeLeo V A, Fowler J F, Fransway A F, Maibach H I, Mathias C G, Nethercott J R, Rietschel R L, Sherertz E F, Storrs F J, Taylor J S
Division of Dermatology, The Pennsylvania State University, College of Medicine, Hershey, USA.
J Am Acad Dermatol. 1998 Jun;38(6 Pt 1):911-8. doi: 10.1016/s0190-9622(98)70587-0.
Allergic contact dermatitis is a significant cause of cutaneous disease affecting many individuals. Patch testing, when used properly, often provides support for the diagnosis of allergic contact dermatitis.
This article reports patch testing results from July 1, 1994, to June 30, 1996, by the North American Contact Dermatitis Group (NACDG).
Patients evaluated in our patch test clinics were tested with the same screening series of allergens by the use of a standardized patch testing technique. The data from these patients were recorded on a standard computer entry form and analyzed.
Forty-nine allergens were tested on 3120 patients. Budesonide was added to the series in July 1995 and tested on 1678 patients. Of these patients, 66.5% had positive allergic patch test reactions, and 57% had at least one allergic reaction that was felt to be clinically relevant to the present or past dermatitis. The 20 screening allergens commercially available to United States dermatologists in the Allergen Patch Test Kit, accounted for only 54.1% of the patients with positive allergic reactions. The additional 30 allergens on the NACDG screening series accounted for 47% of patients with positive allergic reactions. Had the Allergen Patch Test Kit alone been used, 12.4% of all patients tested may have had their disease misclassified as a nonallergic disorder, and an additional 34.4% of all tested patients would not have had their allergies fully defined. Among those patients with positive responses to the supplemental allergens, 81% of the responses were of present or past relevance. The 12 most frequent contact allergens were nickel sulfate, fragrance mix, thimerosal, quaternium-15, neomycin sulfate, formaldehyde, bacitracin, thiuram mix, balsam of Peru, cobalt chloride, para-phenylenediamine, and carba mix. The present relevance varied with the specific allergen from 10.7% (thimerosal) to 85.7% (quaternium-15). Among newer allergens, methyldibromoglutaronitrile/phenoxyethanol (cosmetic preservative) caused positive allergic reactions in 2% of the patients; tixocortol-21-pivalate and budesonide (corticosteroids), in 2.0% and 1.1% of the patients, respectively; and ethylene urea/melamine formaldehyde mix (textile resin), in 5% of the patients.
The usefulness of patch testing is enhanced with the number of allergens tested, because allergens not found on the commercially available screening series in the United States frequently give relevant allergic reactions.
过敏性接触性皮炎是影响众多个体的皮肤疾病的一个重要病因。正确使用斑贴试验通常可为过敏性接触性皮炎的诊断提供依据。
本文报告北美接触性皮炎研究组(NACDG)在1994年7月1日至1996年6月30日期间的斑贴试验结果。
在我们的斑贴试验诊所接受评估的患者,采用标准化斑贴试验技术,用相同的一系列筛查变应原进行检测。这些患者的数据记录在标准的计算机录入表格上并进行分析。
对3120例患者检测了49种变应原。1995年7月将布地奈德加入该系列并对1678例患者进行了检测。在这些患者中,66.5%的患者斑贴试验变应原反应呈阳性,57%的患者至少有1次变应原反应被认为与当前或既往的皮炎在临床上相关。美国皮肤科医生在变应原斑贴试验试剂盒中可获得的20种筛查变应原,仅占变应原反应阳性患者的54.1%。NACDG筛查系列中的另外30种变应原占变应原反应阳性患者的47%。若仅使用变应原斑贴试验试剂盒,所有接受检测的患者中12.4%的疾病可能会被误诊为非过敏性疾病,另外34.4%的所有接受检测的患者的变应原情况将无法得到全面明确。在对补充变应原反应阳性的患者中,81%的反应与当前或既往情况相关。12种最常见的接触性变应原依次为硫酸镍、香料混合物、硫柳汞、季铵盐-15、硫酸新霉素、甲醛、杆菌肽、秋兰姆混合物、秘鲁香脂、氯化钴、对苯二胺和卡巴混合物。当前相关性因具体变应原而异,从10.7%(硫柳汞)到85.7%(季铵盐-15)不等。在较新的变应原中,甲基二溴戊二腈/苯氧乙醇(化妆品防腐剂)在2%的患者中引起变应原反应阳性;21-新戊酸卤倍他索和布地奈德(皮质类固醇)分别在2.0%和1.1%的患者中引起变应原反应阳性;乙烯脲/三聚氰胺甲醛混合物(纺织树脂)在5%的患者中引起变应原反应阳性。
随着检测变应原数量的增加,斑贴试验的效用得到提高,因为在美国市售筛查系列中未发现的变应原常常会引起相关变应原反应。