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A Case of Vesicular Mycosis Fungoides. 水疱性蕈样真菌病1例。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.20.100
Rosa Kim, Bo Ram Kwon, Ji Yeon Byun, You Won Choi, Hae Young Choi, Sanghui Park, Min Young Lee

A 44-year-old male presented with 7 months history of nonpruritic round oozing plaques on the extremities and red papules on the trunk. The lesions were resistant to topical and oral steroid prescribed at the other local clinics. Histopathological examination showed parakeratosis with acanthosis and rete ridge elongation as well as spongiotic intraepidermal blisters and dense dermal infiltration of small to medium sized atypical lymphoid cells. Immunohistochemical analysis revealed the lymphocyte infiltrate to be predominantly CD4+ T cells, with CD4/CD8 ratio to be greater than 10:1. Infiltration of large cells that were CD30+ were also noted. This histopathologic findings are consistent with vesicular mycosis fungoides (MF). He was prescribed with narrow-band ultraviolet B twice per week and topical steroid, combined with interferon-α injection for 5 weeks, and his skin lesions significantly faded and were flattened. Vesicular MF is associated with poor prognosis, but our patient was able to show benign course of disease thanks to timely diagnosis. One must consider vesicular MF as a differential for recalcitrant eczematous lesions.

男性,44岁,四肢有7个月的非瘙痒性圆形渗出斑块,躯干有红色丘疹。病变抵抗局部和口服类固醇处方在其他地方诊所。组织病理学检查显示角化不全伴棘层增生和网状嵴伸长,以及海绵状表皮内水泡和致密的小到中等大小的非典型淋巴样细胞浸润。免疫组化分析显示淋巴细胞浸润以CD4+ T细胞为主,CD4/CD8比值大于10:1。CD30+的大细胞浸润也可见。组织病理学结果与蕈样水疱性真菌病(MF)一致。给予窄带紫外线B每周2次,外用类固醇,并联合干扰素-α注射5周,皮损明显消退、变平。水疱性MF与预后不良有关,但由于及时诊断,我们的患者能够显示出良性病程。必须考虑水泡性MF作为难治性湿疹病变的鉴别诊断。
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引用次数: 0
A Case of Hydroa Vacciniforme-Like Lymphoproliferative Disorder Presenting As Orogenital Ulcerations. 以口腔生殖器溃疡为表现的疫苗样水疱样淋巴增生性疾病1例。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.20.199
Yingyi Li, Yang Wang
Corresponding Author Yang Wang Department of Dermatology and Venerology, Peking University First Hospital, No.8 Xishiku Street, Xicheng District, Beijing 100034, China Tel: +86-10-83572350, Fax: +86-10-66551216, E-mail: yangwang_dr@bjmu.edu.cn https://orcid.org/0000-0001-7805-2861 Dear Editor: Hydroa vacciniforme (HV)-like lymphoproliferative disease (LPD) is associated with chronic active Epstein-Barr virus (CAEBV) infection. It ranges from classic and severe/systemic HV to HV-like lymphoma (HVLL). Cutaneous manifestations include vesiculopapules, bullae, ulcers, and facial swelling. HVLL usually has a long clinical course with spontaneous resolution but may progress to more severe and lifethreatening conditions. We report a rare case of HV-like LPD that evolved from classic HV to orogenital ulcerations. A 17-year-old Chinese boy presented with a 2-month history of painful orogenital swelling and ulcerative lesions without constitutional symptoms. He was diagnosed with classic HV at age 2 years, based on the typical papulovesicular eruptions on his face and photosensitivity. The symptoms spontaneously resolved 2 years before without recurrence, leaving facial varioliform scars (Fig. 1A). Physical examination revealed marked swelling on the lower lip and massive erosions with ulcerations on the scrotum (Fig. 1A, B). No lymphadenopathy was observed. A skin biopsy from the lower lip showed diffuse infiltrates of atypical lymphoid cells throughout the dermis, with remarkable epidermotropism (Fig. 2A). Immunohistochemical analysis revealed CD3+++, CD4+++, Granzyme B++, and TIA1+++ infiltrating lymphocytes, consistent with
{"title":"A Case of Hydroa Vacciniforme-Like Lymphoproliferative Disorder Presenting As Orogenital Ulcerations.","authors":"Yingyi Li,&nbsp;Yang Wang","doi":"10.5021/ad.20.199","DOIUrl":"https://doi.org/10.5021/ad.20.199","url":null,"abstract":"Corresponding Author Yang Wang Department of Dermatology and Venerology, Peking University First Hospital, No.8 Xishiku Street, Xicheng District, Beijing 100034, China Tel: +86-10-83572350, Fax: +86-10-66551216, E-mail: yangwang_dr@bjmu.edu.cn https://orcid.org/0000-0001-7805-2861 Dear Editor: Hydroa vacciniforme (HV)-like lymphoproliferative disease (LPD) is associated with chronic active Epstein-Barr virus (CAEBV) infection. It ranges from classic and severe/systemic HV to HV-like lymphoma (HVLL). Cutaneous manifestations include vesiculopapules, bullae, ulcers, and facial swelling. HVLL usually has a long clinical course with spontaneous resolution but may progress to more severe and lifethreatening conditions. We report a rare case of HV-like LPD that evolved from classic HV to orogenital ulcerations. A 17-year-old Chinese boy presented with a 2-month history of painful orogenital swelling and ulcerative lesions without constitutional symptoms. He was diagnosed with classic HV at age 2 years, based on the typical papulovesicular eruptions on his face and photosensitivity. The symptoms spontaneously resolved 2 years before without recurrence, leaving facial varioliform scars (Fig. 1A). Physical examination revealed marked swelling on the lower lip and massive erosions with ulcerations on the scrotum (Fig. 1A, B). No lymphadenopathy was observed. A skin biopsy from the lower lip showed diffuse infiltrates of atypical lymphoid cells throughout the dermis, with remarkable epidermotropism (Fig. 2A). Immunohistochemical analysis revealed CD3+++, CD4+++, Granzyme B++, and TIA1+++ infiltrating lymphocytes, consistent with","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 5","pages":"389-391"},"PeriodicalIF":1.6,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8e/3d/ad-34-389.PMC9561305.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33489614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Screening of Plant-Derived Natural Extracts to Identify a Candidate Extract Capable of Enhancing Lipid Synthesis in Keratinocytes. 筛选植物来源的天然提取物,以确定能够促进角质形成细胞脂质合成的候选提取物。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.21.288
Sang-Hoon Lee, Hee-Seok Seo, Seong Jun Seo, Chang-Deok Kim, Seung-Phil Hong

Background: Reduced lipid content in the stratum corneum is a major cause of skin-barrier dysfunction in various pathological conditions. Promoting lipid production is a potential strategy to improve skin-barrier function. Recent evidence supports the beneficial effects of adiponectin on lipid metabolism and senescence in keratinocytes.

Objective: This study aimed to investigate whether plant extracts can enhance skin-barrier function.

Methods: We screened fruit and herb extracts that enhance the lipid synthesis of keratinocytes via AMP-activated protein kinase (AMPK) activation and SIRT1 signaling in the adiponectin pathway. The levels of major lipid synthesis enzymes and transcription factors as well as epidermal barrier lipids involved in adiponectin-associated epidermal barrier formation were evaluated in the herbal extracts- or adiponectin-treated human epidermal keratinocyte and equivalent models. The mRNA expression of major lipid synthesis enzymes increased following treatment with Lycii Fructus , Prunus tomentosa , and Melia toosendan extracts.

Results: The expression of transcription factors SIRT1, liver X receptor α, peroxisome proliferator-activated receptors (PPARs), and sterol regulatory element-binding proteins (SREBPs) were upregulated. Levels of free fatty acids, cholesterol, and ceramides were elevated. The expression of keratinocyte differentiation markers increased. In particular, among fruit extracts with a detectable effect, Melia toosendan induced the highest expression of lipid synthase.

Conclusion: These results indicate that Melia toosendan is a promising candidate for improving skin-barrier function.

背景:角质层脂质含量降低是各种病理条件下皮肤屏障功能障碍的主要原因。促进脂质生成是改善皮肤屏障功能的潜在策略。最近的证据支持脂联素对角质形成细胞脂质代谢和衰老的有益作用。目的:研究植物提取物是否具有增强皮肤屏障功能的作用。方法:我们筛选了通过AMPK活化和脂联素通路中SIRT1信号通路促进角质形成细胞脂质合成的水果和草药提取物。在草药提取物或脂联素处理的人表皮角质细胞和等效模型中,评估了主要脂质合成酶和转录因子的水平,以及参与脂联素相关表皮屏障形成的表皮屏障脂质。枸杞子、毛栗和苦楝提取物处理后,主要脂质合成酶mRNA表达增加。结果:转录因子SIRT1、肝脏X受体α、过氧化物酶体增殖激活受体(PPARs)和固醇调节元件结合蛋白(SREBPs)的表达上调。游离脂肪酸、胆固醇和神经酰胺水平升高。角质细胞分化标志物表达增加。在具有显著影响的果实提取物中,香楝诱导脂质合成酶的表达量最高。结论:香楝具有改善皮肤屏障功能的作用。
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引用次数: 1
Hand-Foot-Mouth Disease Mimicking Erythema Multiforme in an Immunocompetent Adult. 免疫功能正常成人模仿多形性红斑的手足口病。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.20.026
Yujin Jung, Yu Ri Woo, Miri Kim, Hyun Jeong Park
Corresponding Author Hyun Jeong Park Department of Dermatology, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 10 63-ro, Yeongdeungpo-gu, Seoul 07345, Korea Tel: +82-2-3779-1230, Fax: +82-2-783-7604, E-mail: hjpark@catholic.ac.kr https://orcid.org/0000-0002-0138-9885 Dear Editor: Hand-foot-mouth disease (HFMD) is a infection caused by Enterovirus and Coxsackievirus that predominantly affects children and symptoms include an erythematous maculopapular or vesicular eruption localized on palms, soles, and perioral skin. Immunocompetent adults recently showed an atypical erythema multiforme (EM)-like eruption. EM is characterized by annular eruption caused by a hypersensitivity reaction from infections such as herpes simplex and mycoplasma pneumonia. Also, unusual viral pathogens Coxsackievirus A6 or A10 have been reported with HFMD, leading to more severe disease course. A 38-year-old male was presented with a pruritic, erythematous maculopapular targetoid eruption on both hands, feet, and trunk for one week (Fig. 1). Initially, he experienced malaise and mild fever before the skin eruption, which did not involve oral mucosa. Blood chemistry tests, rapid plasma reagin, human immunodeficiency virus, and hepatitis serology were normal. Histopathological examination of a macule on his left arm showed neutrophils presented with focal necrosis in upper epidermis and vacuolar alteration in the dermoepidermal junction (Fig. 2). Initially, the patient was misdiagnosed with EM due to clinical exam findings of targetoid lesions. But the additional laboratory examination showed all positive titers of A B
{"title":"Hand-Foot-Mouth Disease Mimicking Erythema Multiforme in an Immunocompetent Adult.","authors":"Yujin Jung,&nbsp;Yu Ri Woo,&nbsp;Miri Kim,&nbsp;Hyun Jeong Park","doi":"10.5021/ad.20.026","DOIUrl":"https://doi.org/10.5021/ad.20.026","url":null,"abstract":"Corresponding Author Hyun Jeong Park Department of Dermatology, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 10 63-ro, Yeongdeungpo-gu, Seoul 07345, Korea Tel: +82-2-3779-1230, Fax: +82-2-783-7604, E-mail: hjpark@catholic.ac.kr https://orcid.org/0000-0002-0138-9885 Dear Editor: Hand-foot-mouth disease (HFMD) is a infection caused by Enterovirus and Coxsackievirus that predominantly affects children and symptoms include an erythematous maculopapular or vesicular eruption localized on palms, soles, and perioral skin. Immunocompetent adults recently showed an atypical erythema multiforme (EM)-like eruption. EM is characterized by annular eruption caused by a hypersensitivity reaction from infections such as herpes simplex and mycoplasma pneumonia. Also, unusual viral pathogens Coxsackievirus A6 or A10 have been reported with HFMD, leading to more severe disease course. A 38-year-old male was presented with a pruritic, erythematous maculopapular targetoid eruption on both hands, feet, and trunk for one week (Fig. 1). Initially, he experienced malaise and mild fever before the skin eruption, which did not involve oral mucosa. Blood chemistry tests, rapid plasma reagin, human immunodeficiency virus, and hepatitis serology were normal. Histopathological examination of a macule on his left arm showed neutrophils presented with focal necrosis in upper epidermis and vacuolar alteration in the dermoepidermal junction (Fig. 2). Initially, the patient was misdiagnosed with EM due to clinical exam findings of targetoid lesions. But the additional laboratory examination showed all positive titers of A B","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 5","pages":"392-393"},"PeriodicalIF":1.6,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/07/5f/ad-34-392.PMC9561299.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33489615","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","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 Adalimumab-Induced Psoriasiform Dermatitis in an Ankylosing Spondylitis Patient: Unusual Progression after Adalimumab Retreatment. 阿达木单抗诱导强直性脊柱炎患者银屑病样皮炎1例:阿达木单抗再治疗后异常进展
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.20.094
Ji Ha Yoon, Joon Woo Jung, Eun Joo Park, Kwang Joong Kim, Kwang Ho Kim
Dear Editor: A 34-year-old Korean man having Ankylosing spondylitis (AS) presented with a 1-month history of lesions on his entire body. We received the patient’s consent form about publishing all photographic materials. Numerous erythematous papules, pustules, and papulosquamous plaques on approximately 25% of the body surface area (Fig. 1). He had been treated with infliximab bimonthly after 2005 for AS, but infliximab had been switched to adalimumab two months before, due to loss of efficacy. After switch, skin eruption aggravated even after application of topical corticosteroid. Results of laboratory examinations were mostly normal. The results of his histopathological examination are shown in Fig. 2. Thick hyperkeratosis, confluent parakeratosis, and elongated rete ridges accompanied by focal spongiosis and exocytosis at the epidermis were noted. Superficial perivascular lymphohistiocytic infiltration was observed in the dermis. Based on clinical manifestations and histopathological findings, adalimumab-induced psoriasiform dermatitis was diagnosed. Clinical progress is summarized in Supplementary Fig. 1. Adalimumab was halted,
{"title":"A Case of Adalimumab-Induced Psoriasiform Dermatitis in an Ankylosing Spondylitis Patient: Unusual Progression after Adalimumab Retreatment.","authors":"Ji Ha Yoon,&nbsp;Joon Woo Jung,&nbsp;Eun Joo Park,&nbsp;Kwang Joong Kim,&nbsp;Kwang Ho Kim","doi":"10.5021/ad.20.094","DOIUrl":"https://doi.org/10.5021/ad.20.094","url":null,"abstract":"Dear Editor: A 34-year-old Korean man having Ankylosing spondylitis (AS) presented with a 1-month history of lesions on his entire body. We received the patient’s consent form about publishing all photographic materials. Numerous erythematous papules, pustules, and papulosquamous plaques on approximately 25% of the body surface area (Fig. 1). He had been treated with infliximab bimonthly after 2005 for AS, but infliximab had been switched to adalimumab two months before, due to loss of efficacy. After switch, skin eruption aggravated even after application of topical corticosteroid. Results of laboratory examinations were mostly normal. The results of his histopathological examination are shown in Fig. 2. Thick hyperkeratosis, confluent parakeratosis, and elongated rete ridges accompanied by focal spongiosis and exocytosis at the epidermis were noted. Superficial perivascular lymphohistiocytic infiltration was observed in the dermis. Based on clinical manifestations and histopathological findings, adalimumab-induced psoriasiform dermatitis was diagnosed. Clinical progress is summarized in Supplementary Fig. 1. Adalimumab was halted,","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 5","pages":"396-398"},"PeriodicalIF":1.6,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/05/3b/ad-34-396.PMC9561303.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33489617","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Evaluation of YouTube Videos about Isotretinoin as Treatment of Acne Vulgaris. YouTube视频对异维甲酸治疗寻常性痤疮的评价。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.21.143
Byeong Chang Ko, Sik Haw

Background: YouTube is one of the most popular video-sharing websites in Korea, but incorrect or biased information is not properly regulated. Acne is common in adolescents and young adults who are familiar with YouTube. Thus, misleading information about isotretinoin in YouTube videos could distort the perception of treatment.

Objective: We evaluated the quality of information about isotretinoin in YouTube videos.

Methods: The keywords searched on YouTube Korea on July 1, 2020 were: isotretinoin, Roaccutane, and Isotinone. The DISCERN tool was used to evaluate the reliability and quality of information, and eight items were used to evaluate scientific accuracy and comprehensiveness: mechanism, indications, dose regimen, contraindications, side effects, blood tests, drug interactions, and pregnancy-related issues.

Results: The number of videos searched was 728. After excluding duplicate or inappropriate videos, 164 videos were analyzed. In the DISCERN tool, the mean overall quality score was 2.24 on a 5-point scale from 1 to 5. The mean score in the 8-issue-criteria, a 3-point scale from 0 to 2, was 0.61. Particularly, indications, blood tests, and drug interactions were poorly addressed in YouTube videos. Medical personnel offer better video quality than non-medical personnel. However, no significant difference in quality existed between the videos of dermatologists and those of other medical personnel. The quality score was not correlated with the popularity of the video.

Conclusion: YouTube videos covering isotretinoin showed poor overall quality. Content quality did not have a significant correlation with popularity, so incorrect information could be propagated on YouTube.

背景:YouTube是韩国最受欢迎的视频分享网站之一,但不正确或有偏见的信息没有得到适当的监管。痤疮在熟悉YouTube的青少年和年轻人中很常见。因此,YouTube视频中关于异维甲酸的误导性信息可能会扭曲对治疗的看法。目的:评价YouTube视频中有关异维甲酸信息的质量。方法:2020年7月1日在韩国YouTube网站上搜索的关键词为:异维甲酸、罗维甲酸、异丁酮。使用DISCERN工具评估信息的可靠性和质量,并使用8个项目评估科学准确性和全面性:机制、适应症、给药方案、禁忌症、副作用、血液检查、药物相互作用和妊娠相关问题。结果:搜索到的视频数为728个。剔除重复或不合适的视频后,分析了164个视频。在DISCERN工具中,从1到5的5分制中,平均总体质量得分为2.24。在8个问题标准(从0到2的3分制)中,平均得分为0.61。特别是,适应症、血液检查和药物相互作用在YouTube视频中没有得到很好的解决。医务人员比非医务人员提供更好的视频质量。然而,皮肤科医生的视频和其他医务人员的视频在质量上没有显著差异。质量分数与视频的受欢迎程度无关。结论:YouTube上涉及异维甲酸的视频整体质量较差。内容质量与受欢迎程度没有显著的相关性,因此可能会在YouTube上传播不正确的信息。
{"title":"Evaluation of YouTube Videos about Isotretinoin as Treatment of Acne Vulgaris.","authors":"Byeong Chang Ko,&nbsp;Sik Haw","doi":"10.5021/ad.21.143","DOIUrl":"https://doi.org/10.5021/ad.21.143","url":null,"abstract":"<p><strong>Background: </strong>YouTube is one of the most popular video-sharing websites in Korea, but incorrect or biased information is not properly regulated. Acne is common in adolescents and young adults who are familiar with YouTube. Thus, misleading information about isotretinoin in YouTube videos could distort the perception of treatment.</p><p><strong>Objective: </strong>We evaluated the quality of information about isotretinoin in YouTube videos.</p><p><strong>Methods: </strong>The keywords searched on YouTube Korea on July 1, 2020 were: isotretinoin, Roaccutane, and Isotinone. The DISCERN tool was used to evaluate the reliability and quality of information, and eight items were used to evaluate scientific accuracy and comprehensiveness: mechanism, indications, dose regimen, contraindications, side effects, blood tests, drug interactions, and pregnancy-related issues.</p><p><strong>Results: </strong>The number of videos searched was 728. After excluding duplicate or inappropriate videos, 164 videos were analyzed. In the DISCERN tool, the mean overall quality score was 2.24 on a 5-point scale from 1 to 5. The mean score in the 8-issue-criteria, a 3-point scale from 0 to 2, was 0.61. Particularly, indications, blood tests, and drug interactions were poorly addressed in YouTube videos. Medical personnel offer better video quality than non-medical personnel. However, no significant difference in quality existed between the videos of dermatologists and those of other medical personnel. The quality score was not correlated with the popularity of the video.</p><p><strong>Conclusion: </strong>YouTube videos covering isotretinoin showed poor overall quality. Content quality did not have a significant correlation with popularity, so incorrect information could be propagated on YouTube.</p>","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 5","pages":"340-348"},"PeriodicalIF":1.6,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d2/48/ad-34-340.PMC9561295.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33489157","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Good Clinical Responders to Topical Timolol in Patients with Infantile Hemangiomas: A 7-Year Retrospective Study of 328 Korean Patients. 婴儿血管瘤患者局部使用替马洛尔有良好的临床反应:328名韩国患者的7年回顾性研究
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.21.203
Da-Ae Yu, Se Hee Min, Jaeryong Song, Jong Seo Park, Hanjae Lee, Jungyoon Ohn, Kyu Han Kim

Background: Topical timolol is widely used for treatment of superficial infantile hemangioma (IH). However, little is known about factors that affect the response to topical timolol treatment.

Objective: This study aimed to investigate the efficacy, safety, and predictive value for good response to topical timolol for IH.

Methods: A retrospective review of medical records and clinical photos of 328 patients with IH treated with topical timolol 0.5% solution was conducted. Serial clinical photographs were compared with those at the initial visit using a 100-mm visual analogue scale (VAS). Treatment response was defined as an improvement of at least 75% from baseline in IH lesions within 12 months of treatment.

Results: Overall, IH patients treated with topical timolol showed significant improvement from baseline, showing that the final VAS score within 12 months of treatment was 69.7±20.4. The multivariable logistic regression analysis showed age at initiation of treatment (p=0.007), length of gestation and fetal growth (p=0.03), depth (p=0.01), and flexural area (p=0.007) were significantly associated with treatment response. Only four patients (1.1%) reported local irritation.

Conclusion: This study demonstrated that topical timolol treatment was an effective and well-tolerated treatment for IHs. Physicians are encouraged to consider several patient- or lesional factors that might affect treatment response to achieve better clinical outcomes.

背景:局部噻洛尔被广泛应用于婴儿浅表性血管瘤的治疗。然而,对影响局部替洛尔治疗反应的因素知之甚少。目的:本研究旨在探讨局部替洛尔治疗IH的疗效、安全性和预测价值。方法:对328例局部应用0.5%替洛尔溶液治疗的IH患者的病历和临床照片进行回顾性分析。使用100毫米视觉模拟量表(VAS)将连续临床照片与初次就诊时的照片进行比较。治疗反应定义为治疗12个月内IH病变较基线改善至少75%。结果:总体而言,局部使用噻洛尔治疗的IH患者较基线有显著改善,治疗12个月内的最终VAS评分为69.7±20.4。多变量logistic回归分析显示,开始治疗时年龄(p=0.007)、妊娠长度和胎儿生长(p=0.03)、深度(p=0.01)和屈折面积(p=0.007)与治疗效果显著相关。只有4例患者(1.1%)报告局部刺激。结论:本研究表明局部替马洛尔治疗IHs是一种有效且耐受性良好的治疗方法。鼓励医生考虑可能影响治疗反应的几个患者或病变因素,以获得更好的临床结果。
{"title":"Good Clinical Responders to Topical Timolol in Patients with Infantile Hemangiomas: A 7-Year Retrospective Study of 328 Korean Patients.","authors":"Da-Ae Yu,&nbsp;Se Hee Min,&nbsp;Jaeryong Song,&nbsp;Jong Seo Park,&nbsp;Hanjae Lee,&nbsp;Jungyoon Ohn,&nbsp;Kyu Han Kim","doi":"10.5021/ad.21.203","DOIUrl":"https://doi.org/10.5021/ad.21.203","url":null,"abstract":"<p><strong>Background: </strong>Topical timolol is widely used for treatment of superficial infantile hemangioma (IH). However, little is known about factors that affect the response to topical timolol treatment.</p><p><strong>Objective: </strong>This study aimed to investigate the efficacy, safety, and predictive value for good response to topical timolol for IH.</p><p><strong>Methods: </strong>A retrospective review of medical records and clinical photos of 328 patients with IH treated with topical timolol 0.5% solution was conducted. Serial clinical photographs were compared with those at the initial visit using a 100-mm visual analogue scale (VAS). Treatment response was defined as an improvement of at least 75% from baseline in IH lesions within 12 months of treatment.</p><p><strong>Results: </strong>Overall, IH patients treated with topical timolol showed significant improvement from baseline, showing that the final VAS score within 12 months of treatment was 69.7±20.4. The multivariable logistic regression analysis showed age at initiation of treatment (<i>p</i>=0.007), length of gestation and fetal growth (<i>p</i>=0.03), depth (<i>p</i>=0.01), and flexural area (<i>p</i>=0.007) were significantly associated with treatment response. Only four patients (1.1%) reported local irritation.</p><p><strong>Conclusion: </strong>This study demonstrated that topical timolol treatment was an effective and well-tolerated treatment for IHs. Physicians are encouraged to consider several patient- or lesional factors that might affect treatment response to achieve better clinical outcomes.</p>","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 5","pages":"360-369"},"PeriodicalIF":1.6,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f0/f0/ad-34-360.PMC9561300.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33489159","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Postherpetic Trigeminal Trophic Syndrome: A Case Report. 带状疱疹后三叉神经营养综合征1例报告。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-10-01 DOI: 10.5021/ad.20.145
Jae-Ho Lee, Ji-An Uh, Joong-Ho Kim, Ho-Young Kim, Myoung-Shin Kim, Un-Ha Lee, Soo-Kyung Lee

Trigeminal trophic syndrome (TTS) is a rare condition characterized by anesthesia, paresthesia, and facial ulceration involving the trigeminal dermatome secondary to self-manipulation of the skin after a peripheral or central injury to the trigeminal nerve or its branches. Differential diagnosis of TTS includes conditions presenting with chronic facial ulceration, such as various infectious diseases, malignancy, vasculitis, pyoderma gangrenosum and dermatitis artefacta. We report a case of postherpetic TTS and highlight the importance of early diagnosis and prompt treatment of this condition, which may commonly be misdiagnosed.

三叉神经营养综合征(TTS)是一种罕见的疾病,其特征是在三叉神经或其分支外周或中枢损伤后,由于皮肤的自我操作而继发的麻醉、感觉异常和面部溃疡累及三叉皮肤组。TTS的鉴别诊断包括表现为慢性面部溃疡的病症,如各种传染病、恶性肿瘤、血管炎、坏疽性脓皮病和人工皮炎。我们报告一例带状疱疹后TTS,并强调早期诊断和及时治疗这种疾病的重要性,这种疾病可能经常被误诊。
{"title":"Postherpetic Trigeminal Trophic Syndrome: A Case Report.","authors":"Jae-Ho Lee,&nbsp;Ji-An Uh,&nbsp;Joong-Ho Kim,&nbsp;Ho-Young Kim,&nbsp;Myoung-Shin Kim,&nbsp;Un-Ha Lee,&nbsp;Soo-Kyung Lee","doi":"10.5021/ad.20.145","DOIUrl":"https://doi.org/10.5021/ad.20.145","url":null,"abstract":"<p><p>Trigeminal trophic syndrome (TTS) is a rare condition characterized by anesthesia, paresthesia, and facial ulceration involving the trigeminal dermatome secondary to self-manipulation of the skin after a peripheral or central injury to the trigeminal nerve or its branches. Differential diagnosis of TTS includes conditions presenting with chronic facial ulceration, such as various infectious diseases, malignancy, vasculitis, pyoderma gangrenosum and dermatitis artefacta. We report a case of postherpetic TTS and highlight the importance of early diagnosis and prompt treatment of this condition, which may commonly be misdiagnosed.</p>","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 5","pages":"378-381"},"PeriodicalIF":1.6,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/75/cc/ad-34-378.PMC9561291.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33489162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Association of Childhood Atopic Dermatitis with Extracutaneous Infections Based on the Nationwide Cross-Sectional Study in Korea. 基于韩国全国横断面研究的儿童特应性皮炎与皮外感染的关系。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-08-01 DOI: 10.5021/ad.20.249
Hee Jae Park, Mira Choi
in the management of various chronic dermatitis a chronic inflammatory skin disease, an immune-mediated inflammatory disease . AD has a lot of infectious complications due to immune dysregulation and skin barrier defects, and it has been reported that the frequency of organ involvement, such as urinary tract infection (UTI), sore throat, ear and simple skin infections, has increased 2-5 . In the case of severe AD, systemic immunosuppressants are widely used, and, as concerns over infectious diseases are recently rising, it is necessary to confirm these complications 6 . Therefore, in this study, we analyzed the association between AD and extracutaneous infections (UTI, pneumonia, otitis media, and sinusitis) in children and ado-lescents based on large-scale data. this a in quartiles pneumonia,
{"title":"Association of Childhood Atopic Dermatitis with Extracutaneous Infections Based on the Nationwide Cross-Sectional Study in Korea.","authors":"Hee Jae Park,&nbsp;Mira Choi","doi":"10.5021/ad.20.249","DOIUrl":"https://doi.org/10.5021/ad.20.249","url":null,"abstract":"in the management of various chronic dermatitis a chronic inflammatory skin disease, an immune-mediated inflammatory disease . AD has a lot of infectious complications due to immune dysregulation and skin barrier defects, and it has been reported that the frequency of organ involvement, such as urinary tract infection (UTI), sore throat, ear and simple skin infections, has increased 2-5 . In the case of severe AD, systemic immunosuppressants are widely used, and, as concerns over infectious diseases are recently rising, it is necessary to confirm these complications 6 . Therefore, in this study, we analyzed the association between AD and extracutaneous infections (UTI, pneumonia, otitis media, and sinusitis) in children and ado-lescents based on large-scale data. this a in quartiles pneumonia,","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 4","pages":"315-317"},"PeriodicalIF":1.6,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3c/c1/ad-34-315.PMC9365646.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40683673","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Thrombophlebitis Migrans As the Prodrome of Adult T-Cell Leukemia-Lymphoma. 移动性血栓性静脉炎是成人t细胞白血病-淋巴瘤的前驱症状。
IF 1.6 4区 医学 Q3 DERMATOLOGY Pub Date : 2022-08-01 DOI: 10.5021/ad.20.184
Haruna Matsuda-Hirose, Yuko Nashimoto, Aki Tanabe, Masao Ogata, Masao Iwao, Kazuhiro Mizukami, Haruto Nishida, Yutaka Hatano
Dear Editor: A 70s male smoker (20 cigarettes/day for 23 years) and human T-lymphotropic virus type 1 (HTLV-1) carrier, developed painful nodular erythema in both wrist joints, the lower extremities and in the testes, each of which underwent 1-month cycles of repeating spontaneous regression and recurrence without any medications. He presented to our hospital 4 months after the initial symptom appeared (data not shown). A biopsy of a representative lesion revealed thrombosis in the deep dermis without leukocytoclastic vasculitis (Fig. 1A). There was neither fibrinoid necrosis nor a granulomatous lesion. A diagnosis of thrombophlebitis migrans was made. The white blood cell count (9,580/μl; normal range 2,950~ 8,970/μl) was increased, with 3% abnormal lymphocytes. Southern blot analysis of peripheral blood revealed an HTLV1 provirus DNA monoclonal band. Serum levels of C-reactive protein (3.57 mg/dl; normal range <0.21 mg/dl), soluble interleukin-2 receptor (2,498 U/ml; normal range 145~519 U/ml) and immunoglobulin A (459 mg/dl; normal range 110~410 mg/dl) also were increased. Because of a history of atrial fibrillation he was taking warfarin, therefore, prothrombin time international-normalized ratio was moderately prolonged (2.13; normal range 0.9~1.1). Protein C, protein S, antithrombin III, and fibrin/fibrinogen degradation products were within normal limits under transient heparinization after interruption of warfarin. Lupus anticoagulant, anticardiolipin antibodies, rapid plasma reagin test, treponema pallidum hemagglutination test and several tumor markers (i.e., squamous cell carcinoma antigen, α-fetoprotein, carcinoembryonic antigen, prostate specific antigen, carbohydrate antigen 19-9) were all negative or within the normal range. Computed tomography (CT) of the total body except for extremities and CT angiography revealed neither a solid mass nor vessel stenosis. His human leukocyte antigen (HLA) alleles were HLA-A*24, A*31, B*07, B*35, which are not associated with Behçet disease. He was diagnosed as smoldering adult T-cell leukemia-lymphoma (ATL) according to the Shimoyama criteria at the initial diagnosis. The clinical course of the present case is described in Fig. 2. Oral administration of rivaroxaban was started instead of warfarin and, thereafter, thrombophlebitis resolved with no further recurrence. Around the disappearance of thrombophlebitis, erythematous maculopapular eruptions were noted to be scattered over the entire body (data not shown); this was followed by HTLV-1-associated arthropathy, and lung disease. Findings of histological findings including immunohistochemical analysis of erythematous areas were consistent with those of ATL (Fig. 1B). His disease status changed to intermediate types between Received July 6, 2020 Revised November 10, 2020 Accepted December 19, 2020
{"title":"Thrombophlebitis Migrans As the Prodrome of Adult T-Cell Leukemia-Lymphoma.","authors":"Haruna Matsuda-Hirose,&nbsp;Yuko Nashimoto,&nbsp;Aki Tanabe,&nbsp;Masao Ogata,&nbsp;Masao Iwao,&nbsp;Kazuhiro Mizukami,&nbsp;Haruto Nishida,&nbsp;Yutaka Hatano","doi":"10.5021/ad.20.184","DOIUrl":"https://doi.org/10.5021/ad.20.184","url":null,"abstract":"Dear Editor: A 70s male smoker (20 cigarettes/day for 23 years) and human T-lymphotropic virus type 1 (HTLV-1) carrier, developed painful nodular erythema in both wrist joints, the lower extremities and in the testes, each of which underwent 1-month cycles of repeating spontaneous regression and recurrence without any medications. He presented to our hospital 4 months after the initial symptom appeared (data not shown). A biopsy of a representative lesion revealed thrombosis in the deep dermis without leukocytoclastic vasculitis (Fig. 1A). There was neither fibrinoid necrosis nor a granulomatous lesion. A diagnosis of thrombophlebitis migrans was made. The white blood cell count (9,580/μl; normal range 2,950~ 8,970/μl) was increased, with 3% abnormal lymphocytes. Southern blot analysis of peripheral blood revealed an HTLV1 provirus DNA monoclonal band. Serum levels of C-reactive protein (3.57 mg/dl; normal range <0.21 mg/dl), soluble interleukin-2 receptor (2,498 U/ml; normal range 145~519 U/ml) and immunoglobulin A (459 mg/dl; normal range 110~410 mg/dl) also were increased. Because of a history of atrial fibrillation he was taking warfarin, therefore, prothrombin time international-normalized ratio was moderately prolonged (2.13; normal range 0.9~1.1). Protein C, protein S, antithrombin III, and fibrin/fibrinogen degradation products were within normal limits under transient heparinization after interruption of warfarin. Lupus anticoagulant, anticardiolipin antibodies, rapid plasma reagin test, treponema pallidum hemagglutination test and several tumor markers (i.e., squamous cell carcinoma antigen, α-fetoprotein, carcinoembryonic antigen, prostate specific antigen, carbohydrate antigen 19-9) were all negative or within the normal range. Computed tomography (CT) of the total body except for extremities and CT angiography revealed neither a solid mass nor vessel stenosis. His human leukocyte antigen (HLA) alleles were HLA-A*24, A*31, B*07, B*35, which are not associated with Behçet disease. He was diagnosed as smoldering adult T-cell leukemia-lymphoma (ATL) according to the Shimoyama criteria at the initial diagnosis. The clinical course of the present case is described in Fig. 2. Oral administration of rivaroxaban was started instead of warfarin and, thereafter, thrombophlebitis resolved with no further recurrence. Around the disappearance of thrombophlebitis, erythematous maculopapular eruptions were noted to be scattered over the entire body (data not shown); this was followed by HTLV-1-associated arthropathy, and lung disease. Findings of histological findings including immunohistochemical analysis of erythematous areas were consistent with those of ATL (Fig. 1B). His disease status changed to intermediate types between Received July 6, 2020 Revised November 10, 2020 Accepted December 19, 2020","PeriodicalId":8233,"journal":{"name":"Annals of Dermatology","volume":"34 4","pages":"312-314"},"PeriodicalIF":1.6,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a7/23/ad-34-312.PMC9365648.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40696498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","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
Annals of Dermatology
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