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Probable apixaban-induced purpura. 可能是阿哌沙班引起的紫癜。
IF 2.3 Q2 ALLERGY Pub Date : 2025-05-01 Epub Date: 2023-08-02 DOI: 10.23822/EurAnnACI.1764-1489.309
G Famularo, F Casorati
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引用次数: 0
Clinical spectrum of patients diagnosed with childhood mastocytosis: a retrospective single center experience. 儿童肥大细胞增多症患者的临床表现:单一中心的回顾性经验。
IF 2.6 Q2 ALLERGY Pub Date : 2025-05-01 Epub Date: 2024-06-24 DOI: 10.23822/EurAnnACI.1764-1489.348
A M Durmaz, Ö Özdemir

Summary: Background. Pediatric cutaneous mastocytosis patients diagnosed and followed up by our specialist were enrolled in this study, and clinical and laboratory evaluations were retrospectively analyzed from patients' archived files. Methods. Patients, who applied to the Division of Pediatric Allergy And Immunology Unit of a University Training and Research Hospital between 01.01.2010 and 28.04.2021, were enrolled in this study. Results. Of the 33 patients included in the study, 11 (33.3%) were female and 22 (67.7%) were male. The median age of onset of the patient's complaints was 7 (0-60) months. The median age at diagnosis was 11 (2-64) months. Their complaints' median regression age was 54 (6-192) months. Resistant clinical findings were followed in 13 (39.4%) patients. Itching, redness, gastrointestinal symptoms, and maculopapular eruption were the most common complaints. The rashes were mostly polymorphic and larger than 1 cm. Heat was the most common trigger. Darier's sign was positive in 97% of the patients. Antihistamines were the most commonly used drug for prophylaxis and treatment. The autoinjector prescription rate was 24.2%. Conclusions. Quality of life was mildly affected in 48,5% of the patients based on the CDLQI scores. Thus, patients should be followed up through adolescence for the development of systemic signs and symptoms.

摘要:背景。本研究选取了由本院专科医生诊断和随访的小儿皮肤肥大细胞增多症患者,并对患者档案中的临床和实验室评估进行了回顾性分析。研究方法研究对象为2010年1月1日至2021年4月28日期间在某大学培训与研究医院儿科过敏与免疫科就诊的患者。研究结果在33名参与研究的患者中,11名(33.3%)为女性,22名(67.7%)为男性。患者发病年龄的中位数为 7(0-60)个月。确诊时的中位年龄为 11(2-64)个月。他们主诉的中位回归年龄为 54(6-192)个月。13例(39.4%)患者出现了抗药性临床症状。瘙痒、发红、胃肠道症状和斑丘疹是最常见的主诉。皮疹大多呈多形性,面积大于 1 厘米。热是最常见的诱发因素。97%的患者达里尔征阳性。抗组胺药是最常用的预防和治疗药物。自动注射器处方率为 24.2%。结论根据 CDLQI 评分,48.5% 的患者生活质量受到轻微影响。因此,应在整个青春期对患者进行随访,以观察其是否出现全身症状和体征。
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引用次数: 0
Clinical severity of LTP syndrome is associated with an expanded IgE repertoire, FDEIA, FDNIH, and LTP mono reactivity. LTP综合征的临床严重程度与扩大的IgE库、FDEIA、FDHIH和LTP单反应性有关。
IF 2.3 Q2 ALLERGY Pub Date : 2025-05-01 Epub Date: 2023-09-15 DOI: 10.23822/EurAnnACI.1764-1489.314
E Scala, D Abeni, V Villella, D Villalta, L Cecchi, V Pravettoni, M Giani, E Caprini, R Asero

Summary: Background. Lipid transfer proteins (LTP) allergy is often a challenge for clinicians. We evaluated a multiplex diagnostic approach with diverse cofactors to stratify LTP syndrome risk. Methods. Of the 1,831 participants screened with 'Allergy Explorer-ALEX-2', 426 had reactions to at least one LTP. Data was gathered and recorded via an electronic database. Results. Reactivity to peach Pru p 3 was found in 77% of individuals with LTP allergy. Higher levels of specific IgE and concurrent sensitization to more than 5 molecules (50% of all LTP-sensitised participants, 62% of symptomatic cases) were significantly associated with an increased risk of severe reactions (p = 0.001). Several cofactors, either alone or in combination, also influenced patients' clinical outcomes. Some cofactors increased the risk of severe reactions, such as mono reactivity to LTP in 44.6% of cases (p = 0.001), Food-Dependent Exercise-Induced Anaphylaxis (FDEIA) in 10.8% of patients (p = 0.001), and Food-dependent NSAID-induced hypersensitivity (FDNIH) in 11.5% (p = 0.005). On the other hand, reactivity to PR10 (24.2%; p = 0.001), profilin hypersensitivity (10.3%; p = 0.001), and/or atopic dermatitis (16.7%; p = 0.001) had a mitigating effect on symptom severity. Conclusions. Clinical severity of LTP syndrome is associated with an expanded IgE repertoire in terms of the number of LTP components recognized and increased IgE levels in individual molecules. Ara h 9, Cor a 8, and Mal d 3 showed the strongest association with clinical severity. In addition, several cofactors may either exacerbate (FDEIA, FDHIH, and LTP monoreactivity) or ameliorate (atopic dermatitis and co-sensitization to profilin and/or PR10) individual patient outcomes. These factors may be utilized for the daily clinical management of LTP syndrome.

摘要:背景。脂质转移蛋白(LTP)过敏通常是临床医生面临的挑战。我们评估了一种具有多种辅助因素的多重诊断方法来对LTP综合征的风险进行分层。方法。在1831名接受“过敏探索者- alex2”筛查的参与者中,426人对至少一种LTP有反应。数据是通过电子数据库收集和记录的。结果。77%的LTP过敏患者对桃子Pru p3有反应。较高水平的特异性IgE和同时致敏超过5个分子(50%的ltp致敏参与者,62%的症状病例)与严重反应的风险增加显著相关(p = 0.001)。几个辅助因素,无论是单独的还是联合的,也会影响患者的临床结果。一些辅助因素增加了严重反应的风险,例如44.6%的病例(p = 0.001)对LTP的单反应性,10.8%的患者(p = 0.001)食物依赖性运动诱导的过敏反应(FDEIA), 11.5%的患者(p = 0.005)食物依赖性非甾体抗炎药诱导的超敏反应(FDNIH)。另一方面,对PR10的反应性为24.2%;P = 0.001), profilin过敏(10.3%;P = 0.001),和/或特应性皮炎(16.7%;P = 0.001)对症状严重程度有缓解作用。结论。LTP综合征的临床严重程度与可识别的LTP成分数量和单个分子中IgE水平的增加有关。Ara h 9、Cor a 8和Mal d 3与临床严重程度的相关性最强。此外,一些辅助因素可能加剧(FDEIA, fdhh和LTP单反应性)或改善(特应性皮炎和对profilin和/或PR10的共同敏感)个体患者的结果。这些因素可用于LTP综合征的日常临床管理。
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引用次数: 0
Pruritus burden assessment in severe atopic dermatitis patients under dupilumab: response predictor? dupilumab治疗严重特应性皮炎患者瘙痒负担评估:反应预测因子?
IF 2.3 Q2 ALLERGY Pub Date : 2025-05-01 Epub Date: 2023-07-28 DOI: 10.23822/EurAnnACI.1764-1489.308
R Brás, R Limão, E Pedro, A Lopes
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引用次数: 0
The autologous serum skin test predicts the response to anti-IgE treatment in chronic spontaneous urticaria patients: a prospective study. 自体血清皮试 (ASST) 预测慢性自发性荨麻疹患者对抗 IgE 治疗的反应:一项前瞻性研究。
IF 2.6 Q2 ALLERGY Pub Date : 2025-05-01 Epub Date: 2024-03-14 DOI: 10.23822/EurAnnACI.1764-1489.337
A Palladino, F Villani, E Pinter, M Visentini, R Asero

Summary: Background. Chronic spontaneous urticaria (CSU), characterized by recurrent itchy wheals and angioedema for > 6 weeks, is a quite common disease that may heavily impair the quality of life. Omalizumab, an anti-IgE mAb, has much improved the management of CSU but patients' response to the drug may vary and predictive markers are still largely missing. We investigated the predictive value of the autologous serum skin test (ASST) on omalizumab response. Methods. 15 patients with severe CSU eligible for omalizumab treatment were prospectively studied submitting them to ASST and to complete blood count, D-dimer, anti-thyroid peroxidase antibodies, and total IgE measurement before the start of the treatment. Results. 14/15 (93%) responded brilliantly to omalizumab at 3 months assessment. 7 responded in less than 1 month ("early responders") and 7 only after multiple administrations ("late responders"). Of 9 patients scoring positive on ASST, 7 (78%) were late, and 2 (22%) early responders to omalizumab (p = 0.021). Of 6 patients scoring negative on ASST, 5 were early omalizumab responders and 1 did not respond. The PPV and NPV of the ASST for a "late" response to omalizumab were 78% and 100%, respectively. Total IgE were significantly higher in early responders. Conclusions. Although larger prospective studies are needed to confirm these results, this study confirms previous retrospective investigations that the positive ASST appears to predict a slow response to omalizumab in CSU patients.

摘要:背景。慢性自发性荨麻疹(CSU)的特点是反复发作的瘙痒性喘鸣和血管性水肿,持续时间超过 6 周,是一种相当常见的疾病,可能严重影响患者的生活质量。抗 IgE mAb 奥马珠单抗(Omalizumab)大大改善了 CSU 的治疗效果,但患者对该药物的反应可能各不相同,而预测性指标在很大程度上仍然缺失。我们研究了自体血清皮试(ASST)对奥马珠单抗反应的预测价值。研究方法对符合奥马珠单抗治疗条件的15例重症CSU患者进行了前瞻性研究,让他们在开始治疗前接受ASST和全血细胞计数、D-二聚体、抗甲状腺过氧化物酶抗体和总IgE测定。结果显示在3个月的评估中,14/15(93%)名患者对奥马珠单抗反应良好。其中 7 人在不到 1 个月的时间内就出现了反应("早期反应者"),7 人在多次用药后才出现反应("晚期反应者")。在 ASST 阳性的 9 名患者中,7 人(78%)对奥马珠单抗反应较晚,2 人(22%)反应较早(p = 0.021)。在 ASST 得分为阴性的 6 名患者中,5 名是奥马珠单抗早期应答者,1 名没有应答。ASST对奥马珠单抗 "晚期 "反应的PPV和NPV分别为78%和100%。早期应答者的总 IgE 明显较高。结论。尽管需要更大规模的前瞻性研究来证实这些结果,但本研究证实了之前的回顾性调查,即 ASST 阳性似乎可预测 CSU 患者对奥马珠单抗的缓慢反应。
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引用次数: 0
Diagnostic accuracy of patch testing based on clinical response to contact allergen restrictions in allergic contact dermatitis. 根据过敏性接触性皮炎患者对接触过敏原限制的临床反应进行斑贴测试的诊断准确性。
IF 2.6 Q2 ALLERGY Pub Date : 2025-05-01 Epub Date: 2024-02-20 DOI: 10.23822/EurAnnACI.1764-1489.331
J Sánchez, L Álvarez, S Diez, J Miquel-Miquel, M Velásquez

Summary: Background. Patch testing (PT) is used to identify substances that cause allergic contact dermatitis (ACD). However, the clinical effects of allergen restrictions following PT have not been thoroughly investigated. This study aims to assess the diagnostic accuracy of PT in patients suspected of having ACD. Methods. Prospective study. PT were performed in patients with clinical diagnosis of ACD. Patients with a positive PT (case group) had a strict restriction of the suspected substance for one month. In patients with negative patch testing (control group), allergen restriction was based in clinical history. Clinical reduction (CR) of at least 50% in disease activity (CR50%) after one month of allergen restriction was considered clinically relevant. Total control was defined as clinical reduction of at least 90% (CR90%). Results. From 400 patients, 66.2% had a positive PT. The sensitivity of PT to identify CR50% was 84%, specificity 47%, PPV 53%, and NPV 81%. Only 10.5% of patients achieved CR90%. Conclusions. The PT had moderate diagnostic accuracy. It could be useful as a screening, but a positive result should be confirmed with controlled allergen restriction. The low number of patients who achieved a 90% CR invites to reconsider the allergens included in PT and the mechanistic processes of the disease.

摘要:背景。斑贴试验(PT)用于确定导致过敏性接触性皮炎(ACD)的物质。然而,对过敏原限制后的临床效果尚未进行深入研究。本研究旨在评估贴片测试对疑似 ACD 患者的诊断准确性。方法:前瞻性研究。前瞻性研究。对临床诊断为 ACD 的患者进行 PT 检查。PT阳性的患者(病例组)在一个月内严格禁用可疑物质。斑贴试验阴性的患者(对照组)则根据临床病史限制使用过敏原。在限制过敏原一个月后,疾病活动的临床缓解(CR)至少达到 50%(CR50%)即为临床相关性。完全控制的定义是临床活动至少减少 90% (CR90%)。结果在 400 名患者中,66.2% 的患者 PT 呈阳性。PT 鉴定 CR50% 的灵敏度为 84%,特异性为 47%,PPV 为 53%,NPV 为 81%。只有 10.5% 的患者达到 CR90%。结论。PT 具有中等诊断准确性。它可作为筛查手段,但阳性结果应通过控制过敏原限制来确认。达到 90% CR 值的患者人数较少,这就需要重新考虑 PT 所包含的过敏原和疾病的机理过程。
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引用次数: 0
A narrative review on allergy and exposure to domestic and non-domestic animals: favorable and unfavorable effects. 关于过敏与接触家畜和非家畜:有利和不利影响的叙述性综述。
IF 2.6 Q2 ALLERGY Pub Date : 2025-05-01 Epub Date: 2024-11-07 DOI: 10.23822/EurAnnACI.1764-1489.372
G Liccardi, M Martini, M B Bilò, L Cecchi, M Milanese, A Musarra, E Puxeddu, P Rogliani

Summary: The aim of this contribution was to highlight the "favorable" and "unfavorable" roles of domestic and non-domestic animals on airway sensitization processes and on the type/severity of the clinical symptoms induced by their exposure. We performed a literature research in MEDLINE for allergic manifestations and animals. Pets can be "allergy friends" through mechanisms related to hygiene hypothesis and translational aspects, the dual role of IgG4 antibodies for pets, and their promising role as healthcare service animals (dogs). On the contrary, animals can be "allergy enemies" when inducing allergic sensitization and  respiratory symptoms (sometimes leading to severe reactions), and also due to cross reactivity with other pets allergens, indirect exposure and ubiquity of their allergens, cross reactivity between Can f 5 and human prostate-specific antigen (PSA). Moreover, in some cases they can trigger anaphylaxis, induce occupational asthma, and act as pests. Finally, we must outline the modest efficacy of allergen immunotherapy (AIT) for their allergens. From a strictly allergological perspective, it is evident that the "negative" aspects resulting from exposure to domestic / non-domestic animals outweigh the "positive" aspects. As a consequence, it is up to humans to seek new ways to balance the pros and cons by exploring research areas that can allow the best possible coexistence with subjects at risk of allergy with domestic and non-domestic animals.

摘要:本文旨在强调家畜和非家畜对气道致敏过程的 "有利 "和 "不利 "作用,以及接触家畜所诱发的临床症状的类型/严重程度。我们在 MEDLINE 上对过敏表现和动物进行了文献研究。通过与卫生假说和转化相关的机制、宠物 IgG4 抗体的双重作用以及宠物作为医疗服务动物(狗)的前景,宠物可以成为 "过敏朋友"。相反,动物也可能成为过敏的 "敌人",因为它们会诱发过敏致敏和呼吸道症状(有时会导致严重反应),还会与其他宠物的过敏原发生交叉反应,间接接触过敏原,过敏原无处不在,Can f 5 与人类前列腺特异性抗原 (PSA) 发生交叉反应。此外,在某些情况下,它们还会引发过敏性休克、诱发职业性哮喘,并成为害虫。最后,我们必须概述一下过敏原免疫疗法(AIT)对其过敏原的适度疗效。从严格的过敏学角度来看,接触家养/非家养动物所产生的 "负面 "影响显然大于 "正面 "影响。因此,人类有责任寻找新的方法来平衡利弊,探索研究领域,让有过敏风险的受试者与家养动物和非家养动物以最佳方式共存。
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引用次数: 0
Anaphylaxis trend before and during pandemic: COVID-19 did not affect anaphylaxis frequency. 大流行前和期间的过敏反应趋势:COVID-19不影响过敏反应频率。
IF 2.6 Q2 ALLERGY Pub Date : 2025-04-29 DOI: 10.23822/EurAnnACI.1764-1489.395
A Sangalli, A Fasiello, V Pravettoni, D Consonni, V Melli, A Jachetti, V Longo, N Montano, F Rivolta

Summary: Background. Data on epidemiology of anaphylaxis are difficult to record. During the lockdown in 2020-2021 due to Coronavirus disease 2019 (COVID-19), referrals to Emergency Department (E.D.) reduced. The aims of the study are to determine anaphylaxis frequency before and during COVID-19 pandemic and risk factors for severity. Methods. Clinical records from a general E.D. of Milan in Italy were retrospectively evaluated before (2018-2019) and during the COVID-19 pandemic (2020-2021) analyzing demographic data, comorbidities, chronic therapies, causes, severity and adrenaline use. Results. The frequency of anaphylaxis remained stable (120/104129 = 0.12% in 2018-2019; 72/66720 = 0.11% in 2020-2021). No differences in the occurrence of anaphylaxis were found in sex and mean age. The main causes of anaphylaxis were food (2018-2019: 53% vs 2020-2021: 51%) and drugs (2018-2019: 27% vs 2020-2021: 33%). Hymenoptera stings had a low occurrence and unidentified trigger was about 15% in each period. The severity of anaphylaxis had a similar distribution in the two periods. Gender and cardiovascular diseases did not influence the severity, instead a positive correlation was found in age over 50 yo (p<0.001). Angiotensin II receptors blockers, β-blockers, diuretics and proton pump inhibitors were associated with increasing severity (p<0.01). Adrenaline administration was similar in the two periods. Conclusions. Anaphylaxis frequency was not affected by the COVID-19 pandemic. Food anaphylaxis remained the most important cause in the urban area. The severity of anaphylaxis was affected by ageing and some chronic therapies, which indirectly point out the role of chronic diseases in the clinical presentation.

摘要:背景。关于过敏反应的流行病学数据很难记录。在2019冠状病毒病(COVID-19)导致的2020-2021年封锁期间,急诊科(ed)的转诊减少了。该研究的目的是确定COVID-19大流行之前和期间的过敏反应频率以及严重程度的危险因素。方法。回顾性评估了意大利米兰一家普通急诊室在2018-2019年和2020-2021年COVID-19大流行之前的临床记录,分析了人口统计数据、合并症、慢性治疗、原因、严重程度和肾上腺素使用情况。结果。2018-2019年,过敏反应发生频率保持稳定(120/104129 = 0.12%;72/66720 = 2020-2021年0.11%)。过敏反应的发生在性别和平均年龄上没有差异。过敏反应的主要原因是食物(2018-2019年:53%,2020-2021年:51%)和药物(2018-2019年:27%,2020-2021年:33%)。膜翅目昆虫蜇伤发生率较低,各时段不明原因蜇伤发生率约为15%。过敏反应的严重程度在两个时期有相似的分布。性别和心血管疾病不影响其严重程度,而在50岁以上的人群中存在正相关(p结论。过敏反应频率不受COVID-19大流行的影响。食物过敏反应仍然是城市地区最重要的原因。过敏反应的严重程度受年龄和一些慢性治疗的影响,这间接指出慢性疾病在临床表现中的作用。
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引用次数: 0
The 2-week time interval criterion may alter the spectrum of disease and patient characteristics in children diagnosed with hypereosinophilia. 2周时间间隔标准可能会改变诊断为嗜酸性粒细胞增多症的儿童的疾病谱和患者特征。
IF 2.6 Q2 ALLERGY Pub Date : 2025-04-29 DOI: 10.23822/EurAnnACI.1764-1489.394
I C Maslak

Summary: Background. Diagnostic criteria for hypereosinophilia (HE) have been revised. Accordingly, the minimum interval between the two results with an absolute eosinophil count (AEC) ≥ 1500 cells/µL has been reduced from 4 to 2 weeks. The aims of this study were to identify patients with HE according to the new diagnostic criteria in children and demonstrate the effects of the revised time interval criterion on patient characteristics and disease spectrum. Methods. Individuals aged ≤ 18 years admitted to a tertiary university hospital were identified using an algorithm based on old and new diagnostic criteria for HE. While patients diagnosed with HE according to old diagnostic criteria were included in group 1, patients who were diagnosed with HE according to the new diagnostic criteria but did not meet the old criteria were included in group 2. Results. Patients in group 1 were significantly older than patients in group 2 at the time of diagnosis of HE (p = 0.004). While the number of patients diagnosed with HE aged 1-5 years was higher in group 1 (p = 0.01), the number of patients diagnosed with HE under the age of one year was higher in group 2 (p = 0.002). The most common cause of HE in group 1 was allergic disorders (10/40, 25%), while non-parasitic infections (17/36, 47%) were the most common diagnosis in group 2. Conclusions. The new diagnostic criteria may change the characteristics of pediatric patients with HE and the spectrum of associated diseases.

摘要:背景。嗜酸性粒细胞增多症(HE)的诊断标准已经修订。因此,绝对嗜酸性粒细胞计数(AEC)≥1500个细胞/µL的两个结果之间的最小间隔从4周减少到2周。本研究的目的是根据新的儿童诊断标准识别患有HE的患者,并证明修订后的时间间隔标准对患者特征和疾病谱系的影响。方法。使用基于新旧HE诊断标准的算法确定了在三级大学医院住院的年龄≤18岁的个体。根据旧诊断标准诊断为HE的患者被纳入1组,而根据新诊断标准诊断为HE但不符合旧诊断标准的患者被纳入2组。结果。组1患者在HE诊断时年龄明显大于组2患者(p = 0.004)。1 ~ 5岁HE患者在组1中较多(p = 0.01), 1岁以下HE患者在组2中较多(p = 0.002)。1组HE最常见的病因为过敏性疾病(10/40,25%),2组最常见的诊断为非寄生虫感染(17/36,47%)。结论。新的诊断标准可能会改变儿童HE患者的特征和相关疾病的谱。
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引用次数: 0
Transitioning from nonspecific therapy to berotralstat in hereditary angioedema type I: real world data from three patients within the same family. 遗传性血管性水肿I型从非特异性治疗过渡到贝曲司他:来自同一家族三名患者的真实世界数据
IF 2.6 Q2 ALLERGY Pub Date : 2025-04-29 DOI: 10.23822/EurAnnACI.1764-1489.391
D Vincent, A Ghanam
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引用次数: 0
期刊
European annals of allergy and clinical immunology
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