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The Journal of dermatology最新文献

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A mutation in the SREBF1 gene resulting in autosomal-dominant ichthyosis Follicularis, Atrichia, and photophobia syndrome. SREBF1基因突变导致常染色体显性鱼鳞病、毛囊性鱼鳞病和畏光综合征。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17474
Bingjie Zheng, Zhihong Zhang, Xing Zhou, Ming Li, Qiufang Qian
{"title":"A mutation in the SREBF1 gene resulting in autosomal-dominant ichthyosis Follicularis, Atrichia, and photophobia syndrome.","authors":"Bingjie Zheng, Zhihong Zhang, Xing Zhou, Ming Li, Qiufang Qian","doi":"10.1111/1346-8138.17474","DOIUrl":"https://doi.org/10.1111/1346-8138.17474","url":null,"abstract":"","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Case report: A novel high-dose intravenous immunoglobulin preparation for the treatment of severe pemphigus vulgaris failing standard therapy. 病例报告：一种新型大剂量静脉注射免疫球蛋白制剂，用于治疗标准疗法无效的重症寻常型天疱疮。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17475
Nadine Wiedenmayer, Katharina Hogrefe, Silvia Mihalceanu, Julia K Winkler, Alexander H Enk
{"title":"Case report: A novel high-dose intravenous immunoglobulin preparation for the treatment of severe pemphigus vulgaris failing standard therapy.","authors":"Nadine Wiedenmayer, Katharina Hogrefe, Silvia Mihalceanu, Julia K Winkler, Alexander H Enk","doi":"10.1111/1346-8138.17475","DOIUrl":"https://doi.org/10.1111/1346-8138.17475","url":null,"abstract":"<p><p>Pemphigus vulgaris (PV) is a severe autoimmune bullous dermatosis that is characterized by autoantibodies against epidermal adhesion proteins causing painful mucosal and skin blistering. Standard treatments for PV include corticosteroids, steroid-sparing immunosuppressants, or intravenous monoclonal anti-CD20-antibody therapy. The European guidelines suggest high-dose intravenous immunoglobulin (IVIg) therapy as a promising approach for severe or treatment-resistant cases. We report on a 65-year-old woman with severe and recurrent disease who achieved long-term disease stabilization with IVIg treatment. Because of recurrent fatigue and headache, the patient was switched to an alternative IVIg preparation with a novel manufacturing process, thus ensuring high purity and better tolerability. We observed excellent efficacy, yet side effects remained largely unchanged. Further studies are necessary to evaluate the long-term efficacy and tolerability of this new IVIg preparation.</p>","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335581","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Successful treatment of nail psoriasis by switching to a TYK2 inhibitor after cyclosporine. 在使用环孢素后改用 TYK2 抑制剂，成功治疗指甲银屑病。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17469
Yuji Kan, Kouhei Horimoto, Hisashi Uhara
{"title":"Successful treatment of nail psoriasis by switching to a TYK2 inhibitor after cyclosporine.","authors":"Yuji Kan, Kouhei Horimoto, Hisashi Uhara","doi":"10.1111/1346-8138.17469","DOIUrl":"https://doi.org/10.1111/1346-8138.17469","url":null,"abstract":"","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335585","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Buruli ulcer: An epidemiological update from Japan. 布路里溃疡：日本流行病学最新进展。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17483
Ryo Fukaura, Manabu Ato, Chiaki Murase, Yuji Miyamoto, Mariko Sugawara-Mikami, Toshifumi Takahashi, Yoshihiko Hoshino, Noriki Fujimoto, Masashi Akiyama, Norihisa Ishii, Rie Yotsu
{"title":"Buruli ulcer: An epidemiological update from Japan.","authors":"Ryo Fukaura, Manabu Ato, Chiaki Murase, Yuji Miyamoto, Mariko Sugawara-Mikami, Toshifumi Takahashi, Yoshihiko Hoshino, Noriki Fujimoto, Masashi Akiyama, Norihisa Ishii, Rie Yotsu","doi":"10.1111/1346-8138.17483","DOIUrl":"https://doi.org/10.1111/1346-8138.17483","url":null,"abstract":"<p><p>Japan is one of the rare non-tropical countries with documented cases of Buruli ulcer (BU). Mycobacterium ulcerans subsp. shinshuense has been identified as the causative agent. The first report of BU in Japan dates back to 1982, with sporadic reports thereafter. Recently, the number of cases has been on the increase, and 50 cases (57.7%) are from the past decade alone, out of a total of 87 cases reported to date. Japan's well-developed healthcare facilities play a crucial role in enabling detailed investigations and providing appropriate treatment for patients, contributing to a favorable prognosis. However, the rarity of the disease results in lack of awareness among healthcare professionals, leading to frequent delays in diagnosis. This article aims to offer an updated overview of BU cases in Japan and to raise awareness of BU among dermatologists and other healthcare professionals in a non-endemic setting.</p>","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of solar urticaria complicated by eosinophilic granulomatosis with polyangiitis treated with mepolizumab. 一例嗜酸性粒细胞肉芽肿伴多血管炎并发日光性荨麻疹患者使用美妥珠单抗治疗。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17479
Mayuko Matsuda, Kimiko Nakajima, Natsuko Aoki, Mayuko Yamamoto, Hideki Nakajima, Hirotaka Yamamoto, Yoshinori Taniguchi, Shin Morizane, Kozo Nakai
{"title":"A case of solar urticaria complicated by eosinophilic granulomatosis with polyangiitis treated with mepolizumab.","authors":"Mayuko Matsuda, Kimiko Nakajima, Natsuko Aoki, Mayuko Yamamoto, Hideki Nakajima, Hirotaka Yamamoto, Yoshinori Taniguchi, Shin Morizane, Kozo Nakai","doi":"10.1111/1346-8138.17479","DOIUrl":"https://doi.org/10.1111/1346-8138.17479","url":null,"abstract":"","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Segmental lichen aureus: A case report of zosteriform distribution and severe pain with literature review. 节段性苔癣：带状分布和剧烈疼痛的病例报告及文献综述。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17486
Jun Yamamoto, Yumi Kambayashi, Shigeru Kuroki, Yoshihide Asano
{"title":"Segmental lichen aureus: A case report of zosteriform distribution and severe pain with literature review.","authors":"Jun Yamamoto, Yumi Kambayashi, Shigeru Kuroki, Yoshihide Asano","doi":"10.1111/1346-8138.17486","DOIUrl":"https://doi.org/10.1111/1346-8138.17486","url":null,"abstract":"","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335583","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Anti-transcription intermediate factor 1-γ antibody-positive dermatomyositis with refractory skin ulcers and rapid cancer progression. 抗转录中间因子 1-γ 抗体阳性的皮肌炎伴有难治性皮肤溃疡和快速癌症进展。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17482
Rika Yamamoto, Hiraku Kokubu, Yasuaki Ikuno, Miwa Kato, Takahiro Koike, Toshifumi Takahashi, Noriki Fujimoto
{"title":"Anti-transcription intermediate factor 1-γ antibody-positive dermatomyositis with refractory skin ulcers and rapid cancer progression.","authors":"Rika Yamamoto, Hiraku Kokubu, Yasuaki Ikuno, Miwa Kato, Takahiro Koike, Toshifumi Takahashi, Noriki Fujimoto","doi":"10.1111/1346-8138.17482","DOIUrl":"https://doi.org/10.1111/1346-8138.17482","url":null,"abstract":"","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Simultaneous skin infection of Mycobacterium chelonae and Nocardia thailandica. 皮肤同时感染克氏分枝杆菌和泰国诺卡氏菌。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17478
Kenta Morimoto, Yutaro Iwamoto, Azusa Kanazawa, Naoko Okiyama
{"title":"Simultaneous skin infection of Mycobacterium chelonae and Nocardia thailandica.","authors":"Kenta Morimoto, Yutaro Iwamoto, Azusa Kanazawa, Naoko Okiyama","doi":"10.1111/1346-8138.17478","DOIUrl":"https://doi.org/10.1111/1346-8138.17478","url":null,"abstract":"","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of chronic spontaneous urticaria with wheals lasting for more than a week. 一个慢性自发性荨麻疹病例，喘息持续时间超过一周。
The Journal of dermatology Pub Date : 2024-09-30 DOI: 10.1111/1346-8138.17480
Satoshi Morioke, Masaya Moriwaki, Akio Tanaka, Michihiro Hide
{"title":"A case of chronic spontaneous urticaria with wheals lasting for more than a week.","authors":"Satoshi Morioke, Masaya Moriwaki, Akio Tanaka, Michihiro Hide","doi":"10.1111/1346-8138.17480","DOIUrl":"https://doi.org/10.1111/1346-8138.17480","url":null,"abstract":"<p><p>Urticaria is characterized by the development of wheals which usually disappear within a day, and are not present beyond a few days. A 58-year-old man began to develop edematous, partially ring-shaped erythematous lesions accompanied by severe body itching without any particular cause, approximately 2 months before his first visit to our hospital. Each rash emerged as being about 5 mm in diameter, gradually enlarging over several days, and disappeared in up to 10 days. Despite oral treatment with several antihistamines and 10 mg of prednisolone, there was no improvement. Most eruptions disappeared without a trace, but the erythema that appeared on the palms left desquamation. The patient had a history of shellfish allergy, but otherwise no atopic diseases. Drug eruption was ruled out due to a lack of regular taking other medications. Histopathological findings of the skin lesions showed moderate lymphocytic and few eosinophilic infiltrates with edema, but no evidence of vasculitis. Despite the concomitant use of two second-generation antihistamines and montelukast, the rash did not improve. The symptoms began to improve following oral intake of 1.5 mg of betamethasone, which was tapered off with the addition of 150 mg of cyclosporin. The use of all medications was stopped at 4 months from the first visit without recurrence. Wheals of chronic spontaneous urticaria may last for longer than a week without apparent histopathological findings of vasculitis.</p>","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142335573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Remission of intercellular IgG/IgA dermatosis after treatment for cervical cancer. 宫颈癌治疗后细胞间 IgG/IgA 皮肤病缓解。
The Journal of dermatology Pub Date : 2024-09-24 DOI: 10.1111/1346-8138.17473
Shohei Kitayama, Keita Takemoto, Yu Matsui, Teruhiko Makino, Megumi Mizawa, Tomoko Shima, Akitoshi Nakashima, Norito Ishii, Takashi Hashimoto, Tadamichi Shimizu
{"title":"Remission of intercellular IgG/IgA dermatosis after treatment for cervical cancer.","authors":"Shohei Kitayama, Keita Takemoto, Yu Matsui, Teruhiko Makino, Megumi Mizawa, Tomoko Shima, Akitoshi Nakashima, Norito Ishii, Takashi Hashimoto, Tadamichi Shimizu","doi":"10.1111/1346-8138.17473","DOIUrl":"https://doi.org/10.1111/1346-8138.17473","url":null,"abstract":"","PeriodicalId":94236,"journal":{"name":"The Journal of dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142309558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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