首页 > 最新文献

Journal of Cutaneous Immunology and Allergy最新文献

英文 中文
Allergic contact dermatitis caused by Dermabond® Advanced: The role of temperature as a potential risk factor 由 Dermabond® Advanced 引起的过敏性接触性皮炎:温度作为潜在风险因素的作用
IF 1 Q4 ALLERGY Pub Date : 2023-09-26 DOI: 10.1002/cia2.12328
Mai Hasegawa MD, Takasuke Ogawa MD, Yumi Ogawa MD, Shigaku Ikeda PhD

We herein report a case of allergic contact dermatitis (ACD) caused by Dermabond® Advanced, which was diagnosed by a patch test using SurgiSeal® (Nitcho Kogyo, Tokyo, Japan) as a control. A difference in the temperature increase at the time of application suggested that temperature may be a risk factor for sensitization.

我们在此报告一例由 Dermabond® Advanced 引起的过敏性接触性皮炎(ACD)病例,该病例是以 SurgiSeal®(日本东京,Nitcho Kogyo)为对照,通过斑贴试验确诊的。使用时温度升高的差异表明,温度可能是导致过敏的一个危险因素。
{"title":"Allergic contact dermatitis caused by Dermabond® Advanced: The role of temperature as a potential risk factor","authors":"Mai Hasegawa MD,&nbsp;Takasuke Ogawa MD,&nbsp;Yumi Ogawa MD,&nbsp;Shigaku Ikeda PhD","doi":"10.1002/cia2.12328","DOIUrl":"10.1002/cia2.12328","url":null,"abstract":"<p>We herein report a case of allergic contact dermatitis (ACD) caused by Dermabond® Advanced, which was diagnosed by a patch test using SurgiSeal® (Nitcho Kogyo, Tokyo, Japan) as a control. A difference in the temperature increase at the time of application suggested that temperature may be a risk factor for sensitization.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 6","pages":"258-259"},"PeriodicalIF":1.0,"publicationDate":"2023-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12328","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135719660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Two cases of acute-onset cystoid macular edema and serous retinal detachment associated with combined use of encorafenib and binimetinib for advanced melanoma: A possible confounding risk for drug intolerance 两例急性囊样黄斑水肿和浆液性视网膜脱离病例与联合使用安戈非尼和宾美替尼治疗晚期黑色素瘤有关:可能存在药物不耐受的混杂风险
IF 1 Q4 ALLERGY Pub Date : 2023-09-20 DOI: 10.1002/cia2.12325
Takumi Hasegawa MD, Shiro Iino MD, PhD, Misako Fujisaki MD, Sayuri Okamura MD, Natsuki Baba MD, PhD, Nami Tanaka MD, Yuko Takeuchi MD, Noritaka Oyama MD, PhD, Minoru Hasegawa MD, PhD

While combined use of BRAF/MEK inhibitors has elicited dramatic clinical efficacy in incurable melanoma, drug-associated retinopathy has become an emerging adverse event. We present two Japanese men with advanced melanoma who developed visual impairment due to serous retinal detachments (SRDs) with cystoid macular edema (CME) immediately after initial administration of encorafenib/binimetinib, a BRAF and MEK inhibitor. One case had drug-intolerable retinopathy on repeat dosing. Both cases were switched to another BRAF/MEK inhibitors, dabrafenib/trametinib, with no recurrence of SRDs. Co-existing CME may be a confounding risk for the early development of SRDs with encorafenib/binimetinib therapy, providing attention during drug administration.

虽然 BRAF/MEK 抑制剂的联合使用在无法治愈的黑色素瘤中取得了显著的临床疗效,但药物相关视网膜病变已成为一种新出现的不良事件。我们报告了两名患有晚期黑色素瘤的日本男性患者,他们在首次服用 BRAF 和 MEK 抑制剂安戈非尼/比尼替尼后,立即出现了浆液性视网膜脱离(SRD)和囊样黄斑水肿(CME),导致视力受损。其中一例患者在重复用药后出现了药物无法耐受的视网膜病变。两例患者都转用了另一种BRAF/MEK抑制剂达拉非尼/曲美替尼,SRD均未复发。并存的CME可能是安戈非尼/比尼美替尼治疗早期发生SRD的一个混杂风险,因此在用药期间应引起注意。
{"title":"Two cases of acute-onset cystoid macular edema and serous retinal detachment associated with combined use of encorafenib and binimetinib for advanced melanoma: A possible confounding risk for drug intolerance","authors":"Takumi Hasegawa MD,&nbsp;Shiro Iino MD, PhD,&nbsp;Misako Fujisaki MD,&nbsp;Sayuri Okamura MD,&nbsp;Natsuki Baba MD, PhD,&nbsp;Nami Tanaka MD,&nbsp;Yuko Takeuchi MD,&nbsp;Noritaka Oyama MD, PhD,&nbsp;Minoru Hasegawa MD, PhD","doi":"10.1002/cia2.12325","DOIUrl":"10.1002/cia2.12325","url":null,"abstract":"<p>While combined use of BRAF/MEK inhibitors has elicited dramatic clinical efficacy in incurable melanoma, drug-associated retinopathy has become an emerging adverse event. We present two Japanese men with advanced melanoma who developed visual impairment due to serous retinal detachments (SRDs) with cystoid macular edema (CME) immediately after initial administration of encorafenib/binimetinib, a BRAF and MEK inhibitor. One case had drug-intolerable retinopathy on repeat dosing. Both cases were switched to another BRAF/MEK inhibitors, dabrafenib/trametinib, with no recurrence of SRDs. Co-existing CME may be a confounding risk for the early development of SRDs with encorafenib/binimetinib therapy, providing attention during drug administration.</p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 6","pages":"231-233"},"PeriodicalIF":1.0,"publicationDate":"2023-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12325","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136310933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of methotrexate-related lymphoproliferative disorder resolved with discontinuation of the drug: A literature review for clinical characteristics in 105 Japanese cases 一例与甲氨蝶呤相关的淋巴组织增生性疾病患者停药后病情得到缓解:有关 105 例日本病例临床特征的文献综述
IF 1 Q4 ALLERGY Pub Date : 2023-09-11 DOI: 10.1002/cia2.12324
Shintaro Higashida MD, Erina Kodaka MD, Hiromichi Iwasaki MD, PhD, Hideaki Sakai MD, Noritaka Oyama MD, PhD, Minoru Hasegawa MD, PhD

We report a case of rheumatoid arthritis who developed cutaneous diffuse large B-cell lymphoma during methotrexate (MTX) monotherapy with prompt resolution after discontinuation of the drug. Our literature review of over 100 reported Japanese cases revisited the potential risk of treatment resistance and/or repeated recurrence of lymphomas, particularly in cases that were unresponsive to the withdrawal of MTX or received a higher cumulative dose.

我们报告了一例类风湿性关节炎患者,该患者在接受甲氨蝶呤(MTX)单药治疗期间出现皮肤弥漫性大B细胞淋巴瘤,停药后病情迅速缓解。我们对 100 多例日本病例的文献进行了回顾,重新审视了治疗耐药性和/或淋巴瘤反复复发的潜在风险,尤其是对停用 MTX 无反应或接受较高累积剂量治疗的病例。
{"title":"A case of methotrexate-related lymphoproliferative disorder resolved with discontinuation of the drug: A literature review for clinical characteristics in 105 Japanese cases","authors":"Shintaro Higashida MD,&nbsp;Erina Kodaka MD,&nbsp;Hiromichi Iwasaki MD, PhD,&nbsp;Hideaki Sakai MD,&nbsp;Noritaka Oyama MD, PhD,&nbsp;Minoru Hasegawa MD, PhD","doi":"10.1002/cia2.12324","DOIUrl":"10.1002/cia2.12324","url":null,"abstract":"<p>We report a case of rheumatoid arthritis who developed cutaneous diffuse large B-cell lymphoma during methotrexate (MTX) monotherapy with prompt resolution after discontinuation of the drug. Our literature review of over 100 reported Japanese cases revisited the potential risk of treatment resistance and/or repeated recurrence of lymphomas, particularly in cases that were unresponsive to the withdrawal of MTX or received a higher cumulative dose.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 6","pages":"255-257"},"PeriodicalIF":1.0,"publicationDate":"2023-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12324","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135938589","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stevens-Johnson syndrome without skin lesions extensively involving the digestive tract 无广泛累及消化道的皮肤病变的Stevens - Johnson综合征
IF 1 Q4 ALLERGY Pub Date : 2023-08-31 DOI: 10.1002/cia2.12323
Yuto Ishikawa MD, Sayaka Ajima MD, Hideo Hashizume MD, PhD

We have experienced a case of SWSL involving significant gastrointestinal erosion that occurred after TMP-SMX medication. For accurate diagnosis and prompt treatment of complications, it is essential to be aware of the possibility of this phenomenon.

我们曾接诊过一例服用 TMP-SMX 后出现严重胃肠道糜烂的 SWSL 病例。为了准确诊断和及时治疗并发症,必须意识到这种现象的可能性。
{"title":"Stevens-Johnson syndrome without skin lesions extensively involving the digestive tract","authors":"Yuto Ishikawa MD,&nbsp;Sayaka Ajima MD,&nbsp;Hideo Hashizume MD, PhD","doi":"10.1002/cia2.12323","DOIUrl":"10.1002/cia2.12323","url":null,"abstract":"<p>We have experienced a case of SWSL involving significant gastrointestinal erosion that occurred after TMP-SMX medication. For accurate diagnosis and prompt treatment of complications, it is essential to be aware of the possibility of this phenomenon.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 6","pages":"249-250"},"PeriodicalIF":1.0,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12323","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48911943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Decreased epidermal AXL expression and increased infiltration of AXL-expressing dendritic cells in psoriasis 银屑病患者表皮AXL表达减少,表达AXL的树突状细胞浸润增加
IF 1 Q4 ALLERGY Pub Date : 2023-08-25 DOI: 10.1002/cia2.12319
Yukiko Ito MD, Sayaka Shibata MD, PhD, Asumi Koyama MD, Lixin Li MD, Eiki Sugimoto MD, Haruka Taira MD, Yuka Mizuno MD, Kentaro Awaji MD, PhD, Shinichi Sato MD, PhD

Background

Psoriasis is a chronic skin inflammatory disease characterized by epidermal proliferation and inflammatory cell infiltration. AXL is a tyrosine kinase receptor that promotes cell proliferation and invasion in cancer cells, and its expression is elevated in multiple tumors. However, less is known about its expression and function in inflammatory diseases.

Objectives

The aim of this study is to examine AXL expression in psoriasis and investigate the biological function of AXL under psoriatic conditions.

Results

AXL mRNA expression was decreased in psoriatic skin compared to healthy skin, and an inverse correlation with neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio was observed. Immunohistochemical staining of psoriatic skin revealed decreased AXL expression of the epidermis and an increased number of AXL-positive dendritic cells in the dermis. Stimulation of epidermal keratinocytes with antimicrobial peptide LL37, but not with IL-17A, resulted in decreased AXL expression. Knockdown of AXL in epidermal keratinocytes did not affect cell proliferation or expression of psoriasis-associated cytokines and chemokines.

Conclusion

Decreased epidermal AXL expression and increased infiltration of AXL-expressing dendritic cells were revealed in psoriasis.

银屑病是一种以表皮增生和炎症细胞浸润为特征的慢性皮肤炎症性疾病。AXL是一种酪氨酸激酶受体,在癌症细胞中促进细胞增殖和侵袭,在多种肿瘤中其表达升高。然而,人们对其在炎症性疾病中的表达和功能知之甚少。本研究的目的是检测AXL在银屑病中的表达,并研究AXL在牛皮癣条件下的生物学功能。与健康皮肤相比,银屑病皮肤中AXL mRNA的表达降低,并且观察到与中性粒细胞与淋巴细胞比率和血小板与淋巴细胞比率呈负相关。银屑病皮肤的免疫组织化学染色显示表皮AXL表达减少,真皮中AXL阳性树突状细胞数量增加。用抗菌肽LL37刺激表皮角质形成细胞,而不是用IL-17A刺激,导致AXL表达降低。表皮角质形成细胞中AXL的敲除不影响细胞增殖或银屑病相关细胞因子和趋化因子的表达。银屑病患者表皮AXL表达降低,表达AXL的树突状细胞浸润增加。
{"title":"Decreased epidermal AXL expression and increased infiltration of AXL-expressing dendritic cells in psoriasis","authors":"Yukiko Ito MD,&nbsp;Sayaka Shibata MD, PhD,&nbsp;Asumi Koyama MD,&nbsp;Lixin Li MD,&nbsp;Eiki Sugimoto MD,&nbsp;Haruka Taira MD,&nbsp;Yuka Mizuno MD,&nbsp;Kentaro Awaji MD, PhD,&nbsp;Shinichi Sato MD, PhD","doi":"10.1002/cia2.12319","DOIUrl":"10.1002/cia2.12319","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Psoriasis is a chronic skin inflammatory disease characterized by epidermal proliferation and inflammatory cell infiltration. AXL is a tyrosine kinase receptor that promotes cell proliferation and invasion in cancer cells, and its expression is elevated in multiple tumors. However, less is known about its expression and function in inflammatory diseases.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>The aim of this study is to examine AXL expression in psoriasis and investigate the biological function of AXL under psoriatic conditions.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>AXL mRNA expression was decreased in psoriatic skin compared to healthy skin, and an inverse correlation with neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio was observed. Immunohistochemical staining of psoriatic skin revealed decreased AXL expression of the epidermis and an increased number of AXL-positive dendritic cells in the dermis. Stimulation of epidermal keratinocytes with antimicrobial peptide LL37, but not with IL-17A, resulted in decreased AXL expression. Knockdown of AXL in epidermal keratinocytes did not affect cell proliferation or expression of psoriasis-associated cytokines and chemokines.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Decreased epidermal AXL expression and increased infiltration of AXL-expressing dendritic cells were revealed in psoriasis.</p>\u0000 </section>\u0000 </div>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 6","pages":"208-218"},"PeriodicalIF":1.0,"publicationDate":"2023-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12319","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48617135","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Normocomplementemic urticarial vasculitis with laryngeal and intestinal tract edema 正常互补性荨麻疹血管炎伴喉部和肠道水肿
IF 1 Q4 ALLERGY Pub Date : 2023-08-09 DOI: 10.1002/cia2.12312
Daisuke Kawakami MD, Yoshiko Oda MD, PhD, Yumi Oka MD, Anri Morita MD, Keiko Kuroda MD, Yoji Hirai MD, PhD, Chikako Nishigori MD, PhD, Atsushi Fukunaga MD, PhD

An 81-year-old Japanese man presented with a history of recurrent eyelid swelling and purpura on the face, neck, and limbs. Because the initial clinical presentation was angioedema alone, the patient was treated with an H1-receptor antagonist and tranexamic acid as for an idiopathic angioedema. The patient also experienced dyspnea simultaneously with edema on the face and limbs and was thus taken to the emergency room, where laryngeal edema was confirmed on laryngeal fiber. A good response to hydrocortisone injection was observed in the patient. ACE inhibitors were never prescribed for the patient, and there was no family history of angioedema. Laboratory data indicated normocomplementemia, and skin biopsies revealed leukocytoclastic vasculitis. Therefore, the patient was diagnosed with NUV. Following hospitalization, the patient experienced appetite loss and the CRP level increased, presenting with thickening and stranding around colon tissues on abdominal CT. These symptoms responded well to prednisone treatment. Given that the initial clinical manifestation of the current case was mainly angioedema, physicians should consider that angioedema may in rare cases be diagnostic for UV.

一位81岁的日本男性,以复发性眼睑肿胀和面部、颈部和四肢紫癜病史提出。由于最初的临床表现仅为血管性水肿,因此患者接受了H1受体拮抗剂和氨甲环酸治疗特发性血管性水肿。患者同时出现呼吸困难,面部和四肢水肿,因此被送往急诊室,喉纤维证实喉水肿。患者对氢化可的松注射反应良好。患者从未开过ACE抑制剂,也没有血管性水肿的家族史。实验室数据显示补体正常,皮肤活检显示白细胞破裂性血管炎。因此,患者被诊断为NUV。住院后,患者出现食欲减退,CRP水平升高,腹部CT表现为结肠组织周围增厚、滞留。这些症状对强的松治疗反应良好。鉴于本病例最初的临床表现主要为血管性水肿,医生应考虑血管性水肿可能在极少数情况下被诊断为紫外线。
{"title":"Normocomplementemic urticarial vasculitis with laryngeal and intestinal tract edema","authors":"Daisuke Kawakami MD,&nbsp;Yoshiko Oda MD, PhD,&nbsp;Yumi Oka MD,&nbsp;Anri Morita MD,&nbsp;Keiko Kuroda MD,&nbsp;Yoji Hirai MD, PhD,&nbsp;Chikako Nishigori MD, PhD,&nbsp;Atsushi Fukunaga MD, PhD","doi":"10.1002/cia2.12312","DOIUrl":"10.1002/cia2.12312","url":null,"abstract":"<p>An 81-year-old Japanese man presented with a history of recurrent eyelid swelling and purpura on the face, neck, and limbs. Because the initial clinical presentation was angioedema alone, the patient was treated with an H1-receptor antagonist and tranexamic acid as for an idiopathic angioedema. The patient also experienced dyspnea simultaneously with edema on the face and limbs and was thus taken to the emergency room, where laryngeal edema was confirmed on laryngeal fiber. A good response to hydrocortisone injection was observed in the patient. ACE inhibitors were never prescribed for the patient, and there was no family history of angioedema. Laboratory data indicated normocomplementemia, and skin biopsies revealed leukocytoclastic vasculitis. Therefore, the patient was diagnosed with NUV. Following hospitalization, the patient experienced appetite loss and the CRP level increased, presenting with thickening and stranding around colon tissues on abdominal CT. These symptoms responded well to prednisone treatment. Given that the initial clinical manifestation of the current case was mainly angioedema, physicians should consider that angioedema may in rare cases be diagnostic for UV.</p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 5","pages":"172-174"},"PeriodicalIF":1.0,"publicationDate":"2023-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12312","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42427882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of disseminated erythematous drug eruption caused by favipiravir in a patient with COVID-19 法匹拉韦致1例COVID - 19患者弥散性红斑药疹
IF 1 Q4 ALLERGY Pub Date : 2023-08-07 DOI: 10.1002/cia2.12321
Aki Honda MD, Toshiyuki Yamamoto MD, PhD

The case of a widespread erythematous drug eruption brought on by favipiravir is described here. Patch tests and the drug lymphocyte transformation test (LTT) both indicated a positive reaction. Since COVID-19 patients take many medications, the potential for a drug eruption must be taken into account when diagnosing a rash.

Favipiravir是一种RNA依赖的RNA聚合酶抑制剂,是一种用于治疗新型或复发性流感感染的药物,也用于治疗目前在全球肆虐的COVID- 19。我们在此报告一例弥散性红斑性药疹,由药物诱导淋巴细胞转化试验(LTT)和斑贴试验结果诊断。42岁日本女性,既往无药疹史,因COVID- 19所致肺炎和肝功能障碍入住呼吸内科,开始使用法匹拉韦治疗。患者在服药后12天(感染发生后第19天)出现发痒疹后转介至我科。首次就诊时,患者出现斑疹样丘疹,全身及面部无黏膜病变(图1)。实验室检查结果:天冬氨酸转氨酶31 U/L(正常范围13 - 30 U/L),丙氨酸转氨酶64 U/L (7 - 23 U/L),乳酸脱氢酶260 U/L (124 - 222 U/L), C反应蛋白2.92 mg/dL (0.3 mg/dL)。考虑到病毒毒性疹或药物疹,我们在入院后停止所有口服药物,并开始口服抗过敏药物。在皮疹和感染愈合后,进行斑贴试验
{"title":"A case of disseminated erythematous drug eruption caused by favipiravir in a patient with COVID-19","authors":"Aki Honda MD,&nbsp;Toshiyuki Yamamoto MD, PhD","doi":"10.1002/cia2.12321","DOIUrl":"10.1002/cia2.12321","url":null,"abstract":"<p>The case of a widespread erythematous drug eruption brought on by favipiravir is described here. Patch tests and the drug lymphocyte transformation test (LTT) both indicated a positive reaction. Since COVID-19 patients take many medications, the potential for a drug eruption must be taken into account when diagnosing a rash.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 5","pages":"201-202"},"PeriodicalIF":1.0,"publicationDate":"2023-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12321","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42624162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The utility of IL36RN mutation analysis in an elderly patient with generalized pustular psoriasis patient treated with secukinumab IL36RN突变分析在接受secukinumab治疗的老年广泛性脓疱性银屑病患者中的应用
IF 1 Q4 ALLERGY Pub Date : 2023-08-06 DOI: 10.1002/cia2.12318
Satoko Minakawa MD, PhD, Yasushi Matsuzaki MD, PhD, Soichiro Watanabe MD, PhD, Kazumitsu Sugiura MD, PhD, Daisuke Sawamura MD, PhD

We present a case of Generalized pustular psoriasis (GPP) presented with SARS-CoV-2 infection under the control of secukinumab. Mutation analysis revealed a heterogeneous c.28C>T (p.Arg10X) mutation in IL36RN. Mutation analysis should be considered to enable preparation for biologic therapy to treat intractable flare-ups.

广义的​脓疱​银屑病​(GPP)​是​具有特征的​通过​严重的​火炬-​ ups​诱发的​通过​各种各样的​因子1​但是​很少的​报告​有​描述​GPP​ 开端​或​火炬-​ups​诱发的​通过​冠状病毒​病​2019​(冠状病毒-​19) 。​ 我们​目前​一​案例​属于​GPP​那个​呈现​具有​SARS-​CoV-​2.​传染​ 在下面​这个​控制​属于​secukinumab。A.​22-​年-​老的​成年女子​呈现​具有​红斑​和​脓疱​在…上​ 她​树干​具有​发烧​在期间​她​第二​怀孕​她​有​不​历史​或​家庭​历史​属于​GPP​或​银屑病​寻常的​在​那个​时间​她​ 有​不​采取​任何​新​药物​之前​这个​火山喷发​开发。​ 我们​已诊断​这个​病人​具有​脓疱病​疱疹样​(IH)。什么时候​她​是​45年​老的​我们​已诊断​这个​病人​具有​GPP​ 之后​ 一​ 第二​ 火炬-​向上的​ 诱发的​ 通过​ 发烧​什么时候​ 她​是​ 59年​ 老的​这个​第三​火炬-​向上的​发生​之后​7天​属于​口头的​非甾体的​反-​ 煽动性的​毒品​治疗​她​有​曾经​管理的​具有​口头的​依曲汀​和​一​有关时事的​类固醇。之后​3个月,​她​已停止​口头的​依曲汀​因为​属于​这个​脱发,​然后​这个​第四​火炬-​向上的​发生。​身体的​检查​揭示​红斑​和​脓疱​在…上​她​树干​和​四肢​(图1A、B)。​ 皮​活组织检查​揭示​Kogoj的​海绵状​脓疱​在里面​这个​表皮​ (图1C)。​ A.​ 由很多种类组成的​ c.28C>T​ (p.Arg10X)​ 突变​ 在里面​ IL36RN​ 基因​ 编码​ 白细胞介素​ (IL)​ 36​ 感受器​ 敌手​ 是​ 揭示​(图1D)。​这个​红斑​部分​已解决​具有​这个​附加​ 属于​ 环孢菌素。​ Secukinumab​是​ 已启动​ 之后​ 一​ 27-​年​ 历史​ 属于​ GPP。​ 随后​ 这个​ 病人​ 有​ 维护​ 完成​缓解​通过​secukinumab​300毫克​每一个​4周​对于​6年​ (图1E、F)。什么时候​她​是​65岁​老的​她​是​已诊断​具有​冠状病毒-​19​ 具有​ 新的-​开端​ 发烧​ 疲劳​ 咳嗽​ 和​ 痰。​ 她​ 临床的​ 课程​ 属于​ 冠状病毒-​19​是​温和的​ 和​ 有​ 不​ 效应​ 在…上​GPP。​我们​ 重新启动​secukinumab​4周​后来​从…起​这个​白天​属于​积极乐观的​具有​这个​ 抗原​检查​配套元件​对于​冠状病毒-​19.Impetigo​疱疹样​是​一​变种​属于​GPP​那个​发展​在期间​ 怀孕。2​ GPP​ 是​ 关联的​具有​突变​ 在里面​ IL36RN.2​ 在…之间​ 10​ IH​病人​属于​东​亚洲的​已报告​在一起​具有​这个​后果​属于​ 遗传的​分析,​7.​有​IL36RN​突变。2​全部的​是​创始人​突变​导致​GPP​在里面​东​亚洲:​c.28C>T​(p.Arg10X)​或​c.115+6T>c​ (p.Arg10ArgfsX1).2英寸​一​学习​比较​治疗​对于​GPP,​在-​医院​死亡率​是​ 降低​ 在里面​这个​生物制品​组​ (1.0%)​比​ 在里面​这个​口头的-​代理人​ 组​ (3.7%)​ 和​ 这个​ 皮质类固醇-​只有​ 组​ (9.1%)​ (p<0.001)。​ 发病率​跟随​这个​相同的​图案:​5.4%​对​8.2%​对​12%,​ 分别地​ (p=.02).3​ 在…之间​ 病人​谁​ 已接收​ 生物制品,​ IL-​ 17​抑制剂​使用​增加​结束​时间​具有​在-​医院​死亡率​和​ 发病率​ 可比较的​ 到​ 那些​ 属于​ 病人​ 拿​ 肿瘤​ 坏死​ 因素​ 抑制剂。3​ IL-​17​ 是​ 关联的​具有​ 这个​ hyper-​煽动性的​ 状态​在里面​冠状病毒-​19;​因此​IL-​17​抑制剂​是​有希望的​目标​ 对于​ 这个​预防​属于​反常的​ 发炎​和​严重的​ 呼吸的​ 忧虑​在里面​冠状病毒-​19.4 A​ 艺术家作品回顾展​ 分析​ 属于​ 10​病人​具有​ 银屑病​谁​已开发​ 冠状病毒-​19​ 在期间​ 治疗​ 具有​ 生物制品​ 显示​ 那个​ 没有一个​已开发​严峻的​症状。​六​病人​已开发​适度的​ 症状,​和​4.​温和的​已开发​症状。5​IL36RN​突变​地位​可以​帮助​预测​产后​火炬-​ ups​在里面​病人​具有​GPP。​这个​突变​分析​是​有用的​对于​GPP​ 妇女​到​使可能​准备​对于​生物学的​治疗​到​对待​棘手的​火炬-​ups。
{"title":"The utility of IL36RN mutation analysis in an elderly patient with generalized pustular psoriasis patient treated with secukinumab","authors":"Satoko Minakawa MD, PhD,&nbsp;Yasushi Matsuzaki MD, PhD,&nbsp;Soichiro Watanabe MD, PhD,&nbsp;Kazumitsu Sugiura MD, PhD,&nbsp;Daisuke Sawamura MD, PhD","doi":"10.1002/cia2.12318","DOIUrl":"10.1002/cia2.12318","url":null,"abstract":"<p>We present a case of Generalized pustular psoriasis (GPP) presented with SARS-CoV-2 infection under the control of secukinumab. Mutation analysis revealed a heterogeneous c.28C&gt;T (p.Arg10X) mutation in IL36RN. Mutation analysis should be considered to enable preparation for biologic therapy to treat intractable flare-ups.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 5","pages":"198-200"},"PeriodicalIF":1.0,"publicationDate":"2023-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12318","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44872302","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Contact dermatitis syndrome to poison ivy 接触性皮炎综合征毒葛
IF 1 Q4 ALLERGY Pub Date : 2023-08-02 DOI: 10.1002/cia2.12320
Marina Seki MD, Marie Suzuki MD, Takehiro Okusa MD, Yuta Ito MD, Tokio Nakada MD
<p>A 7-year-old, otherwise healthy Japanese boy, who lived in Wisconsin State, the United States, developed pruritic rash on his lower extremities 10 days earlier. Since lesions increased in number, he was treated with triamcinolone ointment as eczema at a dermatology clinic in the United States. He then returned to Japan temporarily for a legal matter and was treated with olopatadine hydrochloride, an antihistamine drug, and betamethasone butyrate propionate ointment at a dermatology clinic. Since lesions were not improved despite the treatments described above, the patient was introduced to our department. Figure 1A–D shows a physical examination on his initial visit: We noted vesicles and serous papules and edematous swelling on the left lower thigh (A), papules on the lower back (B), tense blisters on edematous erythema on the right forearm (C), and edematous erythema with papules on left gluteal and femoral regions (D). We suspected contact dermatitis to plants, paint, or resin of bench based on morphology, and those lesions improved by administration of prednisolone, 10 mg for 3 days, and betamethasone butyrate propionate ointment for 7 days. During the interview, we could confirm that poison ivy was growing wild in the yard of the patient's house. As his mother wanted to identify the course, patch testing was performed with Japanese standard series 2015: Patch Test Panel® (S) (the trade name of T.R.U.E. TEST in Japan, Sato Pharmaceutical Co.) and 0.002% urushiol and 0.05% mercuric chloride (Torii Pharmaceutical Co.) 1 month after the initial visit. These were applied on the back for 2 days, and the results read utilizing the International Contact Dermatitis Research Group (ICDRG) scoring system 2 and 6 days after application.<span><sup>1</sup></span> Extremely positive reactions to urushiol were recorded on Days 2 and 6 (Figure 1E). Hence, we diagnosed it as contact dermatitis to poison ivy.</p><p>In Wisconsin State, where the patient lives, poison ivy is considered a typical noxious plant.<span><sup>2</sup></span> It is widely known that urushiol is the causative agent in allergic reactions to poison ivy. Urushiol is a typical causative agent of contact dermatitis in Japan, too. According to the Japanese contact dermatitis research group's tally in 2021, the positive rate to it was 8.7%: The fifth highest rate after gold thiosulfate, nickel sulfate, cobalt chloride, paraphenylenediamine among 24 allergens of the Japanese standard series.<span><sup>3</sup></span> Hence, the Ministry of Foreign Affairs of Japan has issued a warning to travelers to the United States against poison ivy on its website.<span><sup>4</sup></span> In this case, lesions developed not only at contact sites to poison ivy but at noncontact sites like the back and gluteal region. This is a condition that should be called contact dermatitis syndrome<span><sup>5</sup></span> or stage 3A of allergic contact dermatitis syndrome: It is considered that the causative allergen
我们的病例显示对漆酚的强烈过敏反应是过敏性接触性皮炎综合征的3A期。
{"title":"Contact dermatitis syndrome to poison ivy","authors":"Marina Seki MD,&nbsp;Marie Suzuki MD,&nbsp;Takehiro Okusa MD,&nbsp;Yuta Ito MD,&nbsp;Tokio Nakada MD","doi":"10.1002/cia2.12320","DOIUrl":"10.1002/cia2.12320","url":null,"abstract":"&lt;p&gt;A 7-year-old, otherwise healthy Japanese boy, who lived in Wisconsin State, the United States, developed pruritic rash on his lower extremities 10 days earlier. Since lesions increased in number, he was treated with triamcinolone ointment as eczema at a dermatology clinic in the United States. He then returned to Japan temporarily for a legal matter and was treated with olopatadine hydrochloride, an antihistamine drug, and betamethasone butyrate propionate ointment at a dermatology clinic. Since lesions were not improved despite the treatments described above, the patient was introduced to our department. Figure 1A–D shows a physical examination on his initial visit: We noted vesicles and serous papules and edematous swelling on the left lower thigh (A), papules on the lower back (B), tense blisters on edematous erythema on the right forearm (C), and edematous erythema with papules on left gluteal and femoral regions (D). We suspected contact dermatitis to plants, paint, or resin of bench based on morphology, and those lesions improved by administration of prednisolone, 10 mg for 3 days, and betamethasone butyrate propionate ointment for 7 days. During the interview, we could confirm that poison ivy was growing wild in the yard of the patient's house. As his mother wanted to identify the course, patch testing was performed with Japanese standard series 2015: Patch Test Panel® (S) (the trade name of T.R.U.E. TEST in Japan, Sato Pharmaceutical Co.) and 0.002% urushiol and 0.05% mercuric chloride (Torii Pharmaceutical Co.) 1 month after the initial visit. These were applied on the back for 2 days, and the results read utilizing the International Contact Dermatitis Research Group (ICDRG) scoring system 2 and 6 days after application.&lt;span&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/span&gt; Extremely positive reactions to urushiol were recorded on Days 2 and 6 (Figure 1E). Hence, we diagnosed it as contact dermatitis to poison ivy.&lt;/p&gt;&lt;p&gt;In Wisconsin State, where the patient lives, poison ivy is considered a typical noxious plant.&lt;span&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/span&gt; It is widely known that urushiol is the causative agent in allergic reactions to poison ivy. Urushiol is a typical causative agent of contact dermatitis in Japan, too. According to the Japanese contact dermatitis research group's tally in 2021, the positive rate to it was 8.7%: The fifth highest rate after gold thiosulfate, nickel sulfate, cobalt chloride, paraphenylenediamine among 24 allergens of the Japanese standard series.&lt;span&gt;&lt;sup&gt;3&lt;/sup&gt;&lt;/span&gt; Hence, the Ministry of Foreign Affairs of Japan has issued a warning to travelers to the United States against poison ivy on its website.&lt;span&gt;&lt;sup&gt;4&lt;/sup&gt;&lt;/span&gt; In this case, lesions developed not only at contact sites to poison ivy but at noncontact sites like the back and gluteal region. This is a condition that should be called contact dermatitis syndrome&lt;span&gt;&lt;sup&gt;5&lt;/sup&gt;&lt;/span&gt; or stage 3A of allergic contact dermatitis syndrome: It is considered that the causative allergen","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 5","pages":"203-204"},"PeriodicalIF":1.0,"publicationDate":"2023-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12320","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44831853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Respiratory hypersensitivity reaction related to ingestion of raspberry 与摄入树莓有关的呼吸道超敏反应
IF 1 Q4 ALLERGY Pub Date : 2023-08-01 DOI: 10.1002/cia2.12317
Yuki Akamatsu MD, Yoshio Kawakami MD, PhD, Shusaku Fujita MD, Tomoko Kawamoto MD, Tomoko Miyake MD, PhD, Yoji Hirai MD, PhD, Shin Morizane MD, PhD
<p>A 27-year-old woman developed dyspnea and wheezing within 10 min after eating a piece of raspberry walnut cake, and visited an emergency hospital. Based on a presumptive diagnosis of anaphylaxis, she was successfully treated with intravenous corticosteroid and intramuscular injection of adrenaline. She was referred for further investigation. Her medical history included mild asthma, cat allergy, and bipolar disorder, being treated with pranlukast, quetiapine, lamotrigine, and lorazepam. She could eat bread containing wheat and heated eggs without problem after this attack. Laboratory tests showed normal serum level of immunoglobulin (Ig) E 44 IU/mL. Multiple antigen simultaneous test (MAST)-36 (BML Inc) to examine allergen-specific IgE showed 15.2 lumicount (LC) (class 3) of cat dander and 4.89 LC (class 2) of dog dander, whereas the other results were negative. Specific IgE antibodies to strawberry, peach, apple, walnut, Jug r1, egg yolk, egg white, ovomucoid, gluten, ω-5 gliadin, birch pollen tested by CAP fluoro-enzyme immunoassay (CAP-FEIA) and prick-to-prick tests with ingredients of the cake and their related foods, including raspberry, strawberry, blackberry, blueberry, apple, walnut, almond, peanut, wheat, egg yolk, and egg white, were all negative. Then, an open oral provocation test was performed on admission initially with raspberry. Twenty minutes after eating 1.5 pieces of raspberry (about 4.5 g), she developed discomfort of the throat, dyspnea, repetitive cough, audible wheezing, and tachycardia (145 beats/min). Cutaneous symptoms were absent except for mild pruritus of the neck. Her blood pressure and percutaneous oxygen saturation (SpO2) levels were normal. She was treated with intravenous administration of 4 mg betamethasone and 5 mg chlorpheniramine, followed by an intramuscular injection of 0.3 mg adrenaline. Within 10 min, the patient's dyspnea and tachycardia subsided without sequelae. Further investigation with CD203c expression-based basophil activation test (BAT) to raspberry was negative. After avoiding raspberry and all the other berries, as well as still unchallenged walnuts, she has not experienced any episode of acute respiratory reactions for 3 years.</p><p>Raspberry (<i>Rubus idaeus</i>) is a small fruit belonging to the <i>Rosaceae</i> family: subfamily <i>Rosoideae</i> along with strawberry. To the best of our knowledge, there have been only five reported cases of hypersensitivity reactions related to raspberry including our case (Table 1).<span><sup>1-4</sup></span> Three cases had evidence of cross-reactivities with other fruits belonging to <i>Rosaceae</i> family, such as strawberry (<i>n</i> = 2), and/or rPru p 3 (<i>n</i> = 2) from peach.<span><sup>2-4</sup></span> Our case demonstrated negative results on the skin-prick test, which is reliable but not infallible, exhibiting an 85% sensitivity rate.<span><sup>5</sup></span> Despite a lack of cutaneous or mucosal involvement, our case demonstrated the acute
一名27岁的女性在吃了一块覆盆子核桃蛋糕后10分钟内出现呼吸困难和喘息,并前往急救医院。基于过敏反应的推定诊断,她成功地通过静脉注射皮质类固醇和肌肉注射肾上腺素治疗。她被转介接受进一步调查。病史包括轻度哮喘、猫过敏和双相情感障碍,曾用普鲁卡斯特、喹硫平、拉莫三嗪和劳拉西泮治疗。这次发作后,她可以吃含小麦的面包和热鸡蛋了。实验室检查显示血清免疫球蛋白(Ig) E水平正常,为44 IU/mL。多抗原同时检测(MAST)-36 (BML Inc .)检测过敏原特异性IgE的结果显示,猫皮屑的lumicount (LC)(3类)为15.2,狗皮屑的lumicount(2类)为4.89,其他结果均为阴性。用CAP荧光酶免疫法(CAP- feia)检测草莓、桃子、苹果、核桃、Jug r1、蛋黄、蛋清、卵泡样蛋白、面筋、ω-5麦胶蛋白、桦树花粉的特异性IgE抗体,并用覆盆子、草莓、黑莓、蓝莓、苹果、核桃、杏仁、花生、小麦、蛋黄、蛋清等原料进行刺点试验,均为阴性。然后,在入院时进行开放的口腔激发试验,最初使用覆盆子。进食1.5片覆盆子(约4.5 g) 20分钟后,患者出现咽喉不适、呼吸困难、反复咳嗽、可闻喘息、心动过速(145次/分)。除颈部轻微瘙痒外,无皮肤症状。她的血压和经皮氧饱和度(SpO2)水平正常。静脉给予倍他米松4mg、氯苯那敏5mg,随后肌内注射肾上腺素0.3 mg。10分钟内,患者呼吸困难和心动过速消退,无后遗症。进一步研究基于CD203c表达的嗜碱性粒细胞激活试验(BAT)对覆盆子的影响为阴性。在不吃覆盆子和所有其他浆果,以及仍然没有挑战的核桃之后,她3年来没有出现任何急性呼吸反应。树莓(Rubus idaeus)是一种小型水果,属于蔷薇科:与草莓一起属于蔷薇亚科。据我们所知,只有5例与覆盆子相关的过敏反应报告,包括我们的病例(表1)。1-4例与蔷薇科的其他水果有交叉反应的证据,如草莓(n = 2)和/或来自桃子的rPru p3 (n = 2)。2-4本病例的皮肤点刺试验结果为阴性,这是可靠的,但并非绝对正确,敏感性为85%尽管没有皮肤或粘膜受累,我们的病例显示,暴露于可能的过敏原后,急性发作的喉部受累,符合过敏反应诊断的修订标准之一过敏反应通常包括孤立的呼吸道或心血管症状在我们的病例中,桦树的特异性IgE为阴性,在呼吸道症状出现之前,没有观察到口腔粘膜刺痛或水肿症状。因此,我们的病例更有可能被归类为通过胃肠道致敏的1类食物过敏,而不是被归类为口腔过敏综合征。作者声明无利益冲突。批准研究方案:本研究未涉及人类受试者。知情同意:无。注册处及注册编号研究/试验:无。动物研究:无。
{"title":"Respiratory hypersensitivity reaction related to ingestion of raspberry","authors":"Yuki Akamatsu MD,&nbsp;Yoshio Kawakami MD, PhD,&nbsp;Shusaku Fujita MD,&nbsp;Tomoko Kawamoto MD,&nbsp;Tomoko Miyake MD, PhD,&nbsp;Yoji Hirai MD, PhD,&nbsp;Shin Morizane MD, PhD","doi":"10.1002/cia2.12317","DOIUrl":"10.1002/cia2.12317","url":null,"abstract":"&lt;p&gt;A 27-year-old woman developed dyspnea and wheezing within 10 min after eating a piece of raspberry walnut cake, and visited an emergency hospital. Based on a presumptive diagnosis of anaphylaxis, she was successfully treated with intravenous corticosteroid and intramuscular injection of adrenaline. She was referred for further investigation. Her medical history included mild asthma, cat allergy, and bipolar disorder, being treated with pranlukast, quetiapine, lamotrigine, and lorazepam. She could eat bread containing wheat and heated eggs without problem after this attack. Laboratory tests showed normal serum level of immunoglobulin (Ig) E 44 IU/mL. Multiple antigen simultaneous test (MAST)-36 (BML Inc) to examine allergen-specific IgE showed 15.2 lumicount (LC) (class 3) of cat dander and 4.89 LC (class 2) of dog dander, whereas the other results were negative. Specific IgE antibodies to strawberry, peach, apple, walnut, Jug r1, egg yolk, egg white, ovomucoid, gluten, ω-5 gliadin, birch pollen tested by CAP fluoro-enzyme immunoassay (CAP-FEIA) and prick-to-prick tests with ingredients of the cake and their related foods, including raspberry, strawberry, blackberry, blueberry, apple, walnut, almond, peanut, wheat, egg yolk, and egg white, were all negative. Then, an open oral provocation test was performed on admission initially with raspberry. Twenty minutes after eating 1.5 pieces of raspberry (about 4.5 g), she developed discomfort of the throat, dyspnea, repetitive cough, audible wheezing, and tachycardia (145 beats/min). Cutaneous symptoms were absent except for mild pruritus of the neck. Her blood pressure and percutaneous oxygen saturation (SpO2) levels were normal. She was treated with intravenous administration of 4 mg betamethasone and 5 mg chlorpheniramine, followed by an intramuscular injection of 0.3 mg adrenaline. Within 10 min, the patient's dyspnea and tachycardia subsided without sequelae. Further investigation with CD203c expression-based basophil activation test (BAT) to raspberry was negative. After avoiding raspberry and all the other berries, as well as still unchallenged walnuts, she has not experienced any episode of acute respiratory reactions for 3 years.&lt;/p&gt;&lt;p&gt;Raspberry (&lt;i&gt;Rubus idaeus&lt;/i&gt;) is a small fruit belonging to the &lt;i&gt;Rosaceae&lt;/i&gt; family: subfamily &lt;i&gt;Rosoideae&lt;/i&gt; along with strawberry. To the best of our knowledge, there have been only five reported cases of hypersensitivity reactions related to raspberry including our case (Table 1).&lt;span&gt;&lt;sup&gt;1-4&lt;/sup&gt;&lt;/span&gt; Three cases had evidence of cross-reactivities with other fruits belonging to &lt;i&gt;Rosaceae&lt;/i&gt; family, such as strawberry (&lt;i&gt;n&lt;/i&gt; = 2), and/or rPru p 3 (&lt;i&gt;n&lt;/i&gt; = 2) from peach.&lt;span&gt;&lt;sup&gt;2-4&lt;/sup&gt;&lt;/span&gt; Our case demonstrated negative results on the skin-prick test, which is reliable but not infallible, exhibiting an 85% sensitivity rate.&lt;span&gt;&lt;sup&gt;5&lt;/sup&gt;&lt;/span&gt; Despite a lack of cutaneous or mucosal involvement, our case demonstrated the acute","PeriodicalId":15543,"journal":{"name":"Journal of Cutaneous Immunology and Allergy","volume":"6 5","pages":"196-197"},"PeriodicalIF":1.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cia2.12317","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41408158","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Cutaneous Immunology and Allergy
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1