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Frequency of different types of facial melanoses referring to the Department of Dermatology and Venereology, Nepal Medical College and Teaching Hospital in 2019, and assessment of their effect on health-related quality of life. 2019年尼泊尔医学院和教学医院皮肤性病科不同类型面部黑色素瘤的发生频率及其对健康相关生活质量的影响评估
Q2 Medicine Pub Date : 2020-08-03 DOI: 10.1186/s12895-020-00100-3
Bibush Amatya, Anil Kumar Jha, Shristi Shrestha

Background: Abnormalities of facial pigmentation, or facial melanoses, are a common presenting complaint in Nepal and are the result of a diverse range of conditions.

Objectives: The objective of this study was to determine the frequency, underlying cause and impact on quality of life of facial pigmentary disorders among patients visiting the Department of Dermatology and Venereology, Nepal Medical College and Teaching Hospital (NMCTH) over the course of one year.

Methods: This was a cross-sectional study conducted at the Department of Dermatology and Venereology, NMCTH. We recruited patients with facial melanoses above 16 years of age who presented to the outpatient department. Clinical and demographic data were collected and all the enrolled participants completed the validated Nepali version of the Dermatology Life Quality Index (DLQI).

Results: Between January 5, 2019 to January 4, 2020, a total of 485 patients were recruited in the study. The most common diagnoses were melasma (166 patients) and post acne hyperpigmentation (71 patients). Quality of life impairment was highest in patients having melasma with steroid induced rosacea-like dermatitis (DLQI = 13.54 ± 1.30), while it was lowest in participants with ephelides (2.45 ± 1.23).

Conclusion: Facial melanoses are a common presenting complaint and lead to substantial impacts on quality of life. Accurate diagnosis and management can prevent or treat many facial melanoses, including those that lead to substantial loss of quality of life, such as melasma with steroid induced rosacea-like dermatitis. Health care systems in low and middle-income countries should dedicate resources to the identification, prevention and treatment of these conditions to improve quality of life.

背景:面部色素沉着异常,或面部黑色素沉着,是尼泊尔常见的主诉,是多种情况的结果。目的:本研究的目的是确定在尼泊尔医学院和教学医院(NMCTH)皮肤性病科就诊的患者面部色素紊乱的频率、潜在原因及其对生活质量的影响。方法:这是一项在NMCTH皮肤性病科进行的横断面研究。我们招募了16岁以上到门诊部就诊的面部黑色素瘤患者。收集临床和人口统计数据,所有入选的参与者都完成了尼泊尔版的皮肤病学生活质量指数(DLQI)。结果:在2019年1月5日至2020年1月4日期间,共招募了485名患者。最常见的诊断是黄褐斑(166例)和痤疮后色素沉着(71例)。黄褐斑伴类固醇诱发酒渣鼻样皮炎患者的生活质量损害最高(DLQI = 13.54±1.30),而黄褐斑伴黄褐斑患者的DLQI最低(2.45±1.23)。结论:面部黑变是一种常见的主诉,严重影响患者的生活质量。准确的诊断和管理可以预防或治疗许多面部黑色素瘤,包括那些导致生活质量大幅下降的面部黑色素瘤,如黄褐斑与类固醇诱导的酒渣鼻样皮炎。低收入和中等收入国家的卫生保健系统应将资源用于识别、预防和治疗这些疾病,以提高生活质量。
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引用次数: 6
Epidemiology of psoriasis in hard-to-treat body locations: data from the Danish skin cohort. 难以治疗的身体部位牛皮癣的流行病学:来自丹麦皮肤队列的数据。
Q2 Medicine Pub Date : 2020-05-20 DOI: 10.1186/s12895-020-00099-7
Alexander Egeberg, Kyoungah See, Alyssa Garrelts, Russel Burge

Background: Having psoriasis in hard-to-treat areas, i.e. the scalp, face, palms, soles, nails, and genitals, respectively, can impair patients' quality of life. We investigated the prevalence of hard-to-treat body locations of psoriasis, and described patients' clinical and demographic characteristics, and quality of life impacts in a population-based cohort.

Methods: We performed a cross-sectional study using a total of 4016 adults (≥18 years) with psoriasis from the Danish Skin Cohort. Groups were compared to patients without involvement of hard-to-treat areas.

Results: The most frequently affected hard-to-treat area was the scalp (43.0%), followed by the face (29.9%), nails (24.5%), soles (15.6%), genitals (14.1%), and palms (13.7%), respectively. Higher prevalence was generally seen with increasing psoriasis severity. Among all patients 64.8, 42.4, and 21.9% of patients had involvement of ≥1, ≥2, or ≥ 3 hard-to-treat areas. Those with involvement of certain hard-to-treat areas such as hands, feet, and genitals had clinically relevant DLQI impairments. Having involvement of one hard-to-treat area was significantly associated with other hard-to-treat areas affected even after adjusting for age, sex, and psoriasis severity.

Conclusion: Psoriasis commonly affects hard-to-treat locations, even in patients with mild disease. For some of these areas, patient-reported disease burden, e.g. as measured by DLQI, is impaired.

背景:牛皮癣发生在难以治疗的部位,即头皮、面部、手掌、脚底、指甲和生殖器,会损害患者的生活质量。我们调查了银屑病难治性身体部位的患病率,并描述了患者的临床和人口统计学特征,以及以人群为基础的队列的生活质量影响。方法:我们对来自丹麦皮肤队列的4016名患有牛皮癣的成年人(≥18岁)进行了一项横断面研究。将两组患者与未涉及难以治疗区域的患者进行比较。结果:最难治疗的部位为头皮(43.0%),其次为面部(29.9%)、指甲(24.5%)、鞋底(15.6%)、生殖器(14.1%)和手掌(13.7%)。随着银屑病严重程度的增加,患病率普遍较高。在所有患者中,64.8%、42.4和21.9%的患者累及≥1、≥2或≥3个难以治疗区域。那些涉及某些难以治疗的区域,如手、脚和生殖器的人有临床相关的DLQI损伤。即使在调整了年龄、性别和牛皮癣严重程度之后,涉及到一个难以治疗的区域与其他难以治疗的影响区域显著相关。结论:银屑病通常影响难以治疗的部位,即使在病情轻微的患者中也是如此。在其中一些地区,患者报告的疾病负担(例如以DLQI衡量)受到损害。
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引用次数: 40
Osteomyelitis complicating secondarily infected atopic eczema: two case reports and a narrative literature review. 继发感染性特应性湿疹并发骨髓炎:两例报告和一篇叙述性文献回顾。
Q2 Medicine Pub Date : 2020-02-03 DOI: 10.1186/s12895-019-0098-0
Josiah T Masuka, Katherine Troisi, Zamambo Mkhize

Background: Atopic eczema is a relapsing, itchy chronic cutaneous inflammatory disease that commonly affects children. The disease is often complicated by cutaneous infections such as eczema herpeticum, eczema vaccinatum and a varied number of bacterial infections - impetigo, cellulitis and erysipelas. However, rare case reports of infective endocarditis, otitis media and osteo-articular infections have been associated with atopic eczema. These associations possibly represent the extracutaneous infectious complications of atopic eczema.

Case presentation: Here we present two cases of osteomyelitis in HIV negative children with habitual scratching of poorly managed and/or uncontrolled atopic eczema respectively. Both cases presented to the orthopaedic surgeons and were admitted as acute phalangeal osteomyelitis and acute - on - chronic tibial osteomyelitis respectively. The first case was an 8 year old girl who had moderate-severe poorly-controlled atopic eczema and contiguously spread phalangeal osteomyelitis. The second case was an 11 year old pre-pubertal boy who had untreated atopic eczema and tibial osteomyelitis possibly from haematogenously spread Staphylococcus aureus infection. Both were successfully discharged from hospital and currently have well controlled eczema. The 11 year old patient is also being reviewed monthly by the orthopaedic surgeons and is chronic suppressive antibiotics. He may require sequestrectomy, should it be needed.

Conclusions: Invasive staphylococcal and streptococcal osteo-articular (OA) infection can arise as an extra-cutaneous infectious complication of poorly controlled atopic eczema. It is more common in the 3 to 15 year age group and especially in boys with a septic arthritis to osteomyelitis ratio of around 29:5. Clinicians should maintain a high index of suspicion in patients with moderate-severe atopic eczema and they ought to promptly manage these OA infections with intravenous antibiotics to avoid further complications.

背景:特应性湿疹是一种反复发作、发痒的慢性皮肤炎症性疾病,常见于儿童。这种疾病通常伴有皮肤感染,如疱疹性湿疹、疫苗性湿疹和各种细菌感染,如脓疱疮、蜂窝织炎和丹毒。然而,罕见的病例报告,感染性心内膜炎,中耳炎和骨关节感染已与特应性湿疹。这些关联可能代表特应性湿疹的皮外感染并发症。病例介绍:在这里我们提出两个病例骨髓炎的艾滋病毒阴性儿童习惯性抓挠管理不善和/或不受控制的特应性湿疹分别。这两个病例分别以急性指骨骨髓炎和急性非慢性胫骨骨髓炎就诊于骨科。第一例患者为一名8岁女童,患有中重度控制不良的特应性湿疹和连续扩散的指骨骨髓炎。第二个病例是一名11岁的青春期前男孩,他患有未经治疗的特应性湿疹和胫骨骨髓炎,可能是由血源性传播金黄色葡萄球菌感染引起的。两人均顺利出院,目前湿疹控制良好。这名11岁的患者也每月接受骨科医生的检查,并接受慢性抑制抗生素治疗。如果有必要的话,他可能需要切除骨节。结论:侵袭性葡萄球菌和链球菌骨关节(OA)感染可作为控制不良的特应性湿疹的皮外感染并发症出现。脓毒性关节炎与骨髓炎的比例约为29:5,在3至15岁年龄组中更为常见,尤其是男孩。临床医生应对中重度特应性湿疹患者保持高度的怀疑,并应及时用静脉注射抗生素治疗这些OA感染,以避免进一步的并发症。
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引用次数: 4
Madurella mycetomatis infection of the foot: a case report of a neglected tropical disease in a non-endemic region. 足部支足麦氏菌感染:非流行地区一种被忽视的热带病病例报告。
Q2 Medicine Pub Date : 2020-01-10 DOI: 10.1186/s12895-019-0097-1
Basma Karrakchou, Ibtissam Boubnane, Karima Senouci, Badreddine Hassam

Background: Mycetoma is an uncommon chronic granulomatous infection of cutaneous and subcutaneous tissues that can be caused by filamentous bacteria (actinomycetoma) or fungi (eumycetoma). It is the prerogative of young men between the third and fourth decade and is transmitted through any trauma causing an inoculating point. The classic clinical triad associates a painless hard and swelling subcutaneous mass, multiple fistulas, and the pathognomonic discharge of grains. Although endemic in many tropical and subtropical countries, mycetoma can also be found in non-endemic areas as in Morocco, and causes then diagnosis problems leading to long lasting complications. Therefore, we should raise awareness of this neglected disease for an earlier management. Under medical treatment however, mycetoma has a slow healing and surgery is often needed, and relapses are possible.

Case presentation: Herein we report a case of a 64 years old patient, with a history of eumycetoma occurring ten years ago treated with oral terbinafine coupled with surgery. A complete remission was seen after 2 years. He presented a relapse on the previous scar 6 months ago. There wasn't any bone involvement in the magnetic resonance imaging (MRI). The patient was put under oral terbinafine with a slow but positive outcome.

Conclusion: Through this case report, we perform a literature review and highlight the importance of increase awareness of mycetoma in clinical practice especially in non-endemic regions.

背景:足菌肿是一种罕见的皮肤和皮下组织慢性肉芽肿感染,可由丝状细菌(放线菌瘤)或真菌(真菌瘤)引起。它是第三和第四个十年之间的年轻人的特权,并通过造成接种点的任何创伤传播。典型的临床三联征包括无痛、坚硬和肿胀的皮下肿块、多个瘘管和典型的颗粒排出。尽管足菌肿在许多热带和亚热带国家流行,但也可在摩洛哥等非流行地区发现,并造成诊断问题,导致长期并发症。因此,我们应该提高对这种被忽视疾病的认识,以便及早治疗。然而,在医学治疗下,足菌肿愈合缓慢,经常需要手术,并且有可能复发。病例介绍:在此,我们报告一例64岁的患者,有十年前发生的脓肿史,口服特比萘芬联合手术治疗。2年后完全缓解。他六个月前的伤疤又复发了。磁共振成像(MRI)未见骨受累。患者口服特比萘芬,结果缓慢但积极。结论:通过本病例报告,我们进行了文献回顾,并强调在临床实践中提高对足菌肿的认识的重要性,特别是在非流行地区。
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引用次数: 12
A rare case of Sweet syndrome secondary to melioidosis 一例罕见的类鼻疽继发Sweet综合征
Q2 Medicine Pub Date : 2019-12-02 DOI: 10.1186/s12895-019-0096-2
S. Vithoosan, B. Thanushah, P. Piranavan, D. Gamlaksha, H. Karunatilake, A. Jayanaga
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引用次数: 4
High efficacy of a dimeticone-based pediculicide following a brief application: in vitro assays and randomized controlled investigator-blinded clinical trial 一种基于二聚体酮的修脚剂在短暂应用后的高效性:体外试验和随机对照研究者盲法临床试验
Q2 Medicine Pub Date : 2019-10-18 DOI: 10.1186/s12895-019-0094-4
J. Heukelbach, Doerte Wolf, J. Clark, H. Dautel, Kristina Roeschmann
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引用次数: 9
Comparative efficacy of three pediculicides to treat head lice infestation in primary school girls: a randomised controlled assessor blind trial in rural Iran 三种修脚剂治疗小学女生头虱感染的疗效比较:一项在伊朗农村进行的随机对照评估盲试验
Q2 Medicine Pub Date : 2019-09-12 DOI: 10.1186/s12895-019-0093-5
Hadi Kalari, Aboozar Soltani, K. Azizi, H. Faramarzi, M. Moemenbellah-Fard
{"title":"Comparative efficacy of three pediculicides to treat head lice infestation in primary school girls: a randomised controlled assessor blind trial in rural Iran","authors":"Hadi Kalari, Aboozar Soltani, K. Azizi, H. Faramarzi, M. Moemenbellah-Fard","doi":"10.1186/s12895-019-0093-5","DOIUrl":"https://doi.org/10.1186/s12895-019-0093-5","url":null,"abstract":"","PeriodicalId":9014,"journal":{"name":"BMC Dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12895-019-0093-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49493305","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: 17
Validation of the Atopic Dermatitis Control Tool (ADCT©) using a longitudinal survey of biologic-treated patients with atopic dermatitis 使用生物治疗的特应性皮炎患者的纵向调查验证特应性皮肤炎控制工具(ADCT©)
Q2 Medicine Pub Date : 2019-09-03 DOI: 10.1186/s12895-019-0095-3
E. Simpson, L. Eckert, A. Gadkari, U. Mallya, Min Yang, L. Nelson, Michelle Brown, M. Reaney, P. Mahajan, I. Guillemin, M. Boguniewicz, D. Pariser
{"title":"Validation of the Atopic Dermatitis Control Tool (ADCT©) using a longitudinal survey of biologic-treated patients with atopic dermatitis","authors":"E. Simpson, L. Eckert, A. Gadkari, U. Mallya, Min Yang, L. Nelson, Michelle Brown, M. Reaney, P. Mahajan, I. Guillemin, M. Boguniewicz, D. Pariser","doi":"10.1186/s12895-019-0095-3","DOIUrl":"https://doi.org/10.1186/s12895-019-0095-3","url":null,"abstract":"","PeriodicalId":9014,"journal":{"name":"BMC Dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12895-019-0095-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45832266","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: 43
Ainhum, a rare mutilating dermatological disease in a female Cameroonian: a case report 喀麦隆女性罕见的肢解性皮肤病Ainhum病例报告
Q2 Medicine Pub Date : 2019-08-12 DOI: 10.1186/s12895-019-0092-6
D. Tchouakam, J. Tochie, M. Guifo, S. Choukem
{"title":"Ainhum, a rare mutilating dermatological disease in a female Cameroonian: a case report","authors":"D. Tchouakam, J. Tochie, M. Guifo, S. Choukem","doi":"10.1186/s12895-019-0092-6","DOIUrl":"https://doi.org/10.1186/s12895-019-0092-6","url":null,"abstract":"","PeriodicalId":9014,"journal":{"name":"BMC Dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12895-019-0092-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49299102","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: 7
Gluteal hidradenitis suppurativa presenting pemphigus-like findings: case report 臀汗腺化脓性炎表现为天疱疮样表现:1例报告
Q2 Medicine Pub Date : 2019-07-23 DOI: 10.1186/s12895-019-0091-7
Y. Kurihara, M. Furue
{"title":"Gluteal hidradenitis suppurativa presenting pemphigus-like findings: case report","authors":"Y. Kurihara, M. Furue","doi":"10.1186/s12895-019-0091-7","DOIUrl":"https://doi.org/10.1186/s12895-019-0091-7","url":null,"abstract":"","PeriodicalId":9014,"journal":{"name":"BMC Dermatology","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12895-019-0091-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41544139","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: 1
期刊
BMC Dermatology
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