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Indian Journal of Paediatric Dermatology最新文献

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A Review of Dermal Melanocytosis 皮肤黑色素细胞增多症的研究进展
Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_66_22
Manjyot Gautam, Kajomi Shingala
Abstract Dermal melanocytosis is a histological term used to describe a clinical spectrum of cutaneous diseases which present as bluish-gray pigmentation of the skin. The most common forms include the Mongolian spot (MS), nevus of Ota, nevus of Ito, and dermal melanocyte hamartoma sharing similar etiologies and histologic findings but different associations and prognosis. Although these lesions usually resolve by 1 to 2 years of age, widespread aberrant MSs, nevus of Ota, and nevus of Ito can persist into adulthood and can become a great concern for the patients regarding the pigmentation and health risk associated with the same. An extensive literature search was done; all clinical trials, randomized double-blind or single-blind controlled trials, open-label studies, retrospective studies, reviews, case series, and case reports concerned with dermal melanocytosis were screened. The selected articles were retrieved; the final manuscript was prepared, analyzed, and presented in a narrative fashion.
皮肤黑色素细胞增多症是一个组织学术语,用于描述皮肤疾病的临床谱,其表现为皮肤的蓝灰色色素沉着。最常见的形式包括蒙古斑(MS)、太田痣、伊藤痣和皮肤黑素细胞错构瘤,它们具有相似的病因和组织学表现,但不同的关联和预后。虽然这些病变通常在1至2岁时消退,但广泛的异常MSs、太田痣和伊藤痣可持续到成年,并可能成为患者对色素沉着和相关健康风险的极大关注。进行了广泛的文献检索;筛选了所有与皮肤黑色素细胞增多症有关的临床试验、随机双盲或单盲对照试验、开放标签研究、回顾性研究、综述、病例系列和病例报告。检索选定的文章;最后的手稿被准备、分析,并以叙述的方式呈现。
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引用次数: 0
The diagnostic dilemma of patchy hair loss 斑驳脱发的诊断困境
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_20_22
R. Agarwal, Chakraborty Abhijit, B. Chandrashekar, S. Dhar
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引用次数: 0
Waardenburg syndrome with rare ocular features 伴有罕见眼部特征的Waardenburg综合征
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_172_21
N. Puri, Sheenu Goyal, B. Brar
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引用次数: 0
Annular erythema of infancy in a neonate 新生儿的环状红斑
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_3_22
Sabha Mushtaq
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引用次数: 0
Is there a role for combined therapy with oral corticosteroids and propranolol in patients with infantile hemangioma? A retrospective cohort study 口服皮质类固醇和心得安在婴幼儿血管瘤患者中联合治疗是否有作用?回顾性队列研究
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_5_22
Luz Orozco-Covarrubias, Claudia E García-Valencia, M. Sáez-de-Ocariz
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引用次数: 0
Chronic Lingual Papulosis in a Pediatric Patient 慢性舌丘疹病的儿科患者
Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_15_23
Apoorva Sharma, Akash P. Mustari, Rahul Mahajan
An 8-year-old male presented with fissuring of the tongue and occasional burning sensation over the tongue while eating of two years duration. On examination, multiple pinkish translucent non-tender papules of uniform size with multiple linear fissures were seen on the dorsum and lateral border of the tongue [Figure 1]. The rest of the oral mucosa and systemic examination were within normal limits. A diagnosis of chronic lingual papulosis (CLP) associated with fissured tongue was arrived at based on classical clinical presentation and the lack of any systemic/syndromic features. The patient was counselled regarding the benign nature of the disease and was given topical benzocaine gel for mild episodic burning sensation. After 1 year of follow-up, the patient reported no change in the severity of the symptoms or lesions.Figure 1: Multiple pinkish translucent papules of uniform size with multiple linear fissures over the dorsum of the tongueCLP is a hyperplastic response of filiform and fungiform papillae, most commonly seen as focal or diffuse enlargement of numerous pinkish to pale translucent papules of uniform size over the dorsum and tip of the tongue. It usually has an adult onset; however, pediatric cases have also been described. The etiology is possibly developmental rather than inflammatory and, therefore, it would be logical to refer to the childhood-onset cases as “congenital CLP” or “developmental CLP.”[1] The common differential diagnoses of translucent papules over the tongue are CLP and transient lingual papillitis (TLP). TLP is most commonly seen in its classic form as painful enlarged papillae due to acute or chronic local irritation or trauma and compulsive tongue movement. The exact etiology of TLP is unknown and probably multifactorial, as it can be hypothesized by the variable and non-specific histological findings.[2] A painless papulo-keratotic variant has also been reported.[2,3] TLP can be differentiated from CLP by the presence of transient lesions in the former. CLP usually does not require a histopathological confirmation of diagnosis unless associated with atypical features or associated systemic features and does not require active management unless secondarily infected by Candida. Recognizing this benign entity is important for dermatologists to avoid unnecessary investigations and interventions. Declaration of patient consent The authors certify that they have obtained all appropriate consent forms, duly signed by the parent(s)/guardian(s) of the patient. In the form, the parent(s)/guardian(s) has/have given his/her/their consent for the images and other clinical information of their child to be reported in the journal. The parents understand that the names and initials of their child/children will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.
一名八岁男性,在进食时出现舌裂及偶尔舌上灼烧感,持续两年。检查时,舌背侧缘可见多个大小均匀的粉红色半透明无压痛丘疹,伴多条线状裂隙[图1]。其余口腔黏膜及全身检查均正常。慢性舌丘疹病(CLP)合并舌裂的诊断是基于经典的临床表现和缺乏任何系统性/综合征特征。患者被告知疾病的良性性质,并给予局部苯佐卡因凝胶轻度发作性烧灼感。经过1年的随访,患者报告症状或病变的严重程度没有变化。图1:舌背上多个大小均匀的粉红色半透明丘疹,并伴有多个线状裂隙。eclp是丝状和真菌状乳头的增生反应,最常见的表现是舌背和舌尖上许多大小均匀的粉红色至苍白半透明丘疹的局灶性或弥漫性扩大。它通常在成人发病;然而,儿童病例也有描述。病因可能是发育性而非炎症性,因此,将儿童期发病病例称为“先天性CLP”或“发育性CLP”是合乎逻辑的。舌上半透明丘疹的常见鉴别诊断是CLP和短暂性舌乳头炎。TLP最常见的典型表现是由于急性或慢性局部刺激或创伤以及强迫性舌头运动而导致的疼痛的乳头状肿大。TLP的确切病因尚不清楚,可能是多因素的,因为它可以通过可变和非特异性的组织学发现来假设无痛丘疹角化异型也有报道。[2,3] TLP与CLP的区别在于前者有短暂病变。CLP通常不需要组织病理学诊断,除非伴有非典型特征或相关的全身特征,除非继发感染念珠菌,否则不需要积极治疗。认识到这种良性实体对皮肤科医生避免不必要的调查和干预很重要。患者同意声明作者证明他们已经获得了所有适当的同意书,并由患者的父母/监护人正式签署。在此表格中,家长/监护人已经/已经同意其孩子的图像和其他临床信息将在杂志上报道。家长明白他们孩子的名字和首字母不会被公布,并会尽力隐藏他们的身份,但不能保证匿名。财政支持及赞助无。利益冲突没有利益冲突。
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引用次数: 0
Ectodermal dysplasia-skin fragility syndrome in an infant 婴儿外胚层发育不良-皮肤脆性综合征
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_18_22
Sabha Mushtaq, Abhirut Thakur
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引用次数: 0
A case report of xanthoma in a child: A sign of systemic disease 儿童黄瘤1例:全身性疾病的征兆
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_178_21
Karthik Sunki, B. Katakam, GNarsimha Rao Netha, S. Rani
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引用次数: 0
Hair transplantation by follicular unit extraction in cicatricial alopecia in children 毛囊单位提取毛发移植治疗儿童瘢痕性脱发
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_68_22
J. Buch, K. Chouhan
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引用次数: 0
Dedicator of cytokinesis 8 immunodeficiency syndrome presenting as extensive and giant lesions of molluscum contagiosum in a child 细胞分裂8免疫缺陷综合征的奉献者,表现为儿童传染性软疣的广泛和巨大病变
IF 0.2 Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.4103/ijpd.ijpd_10_22
S. Tambe, K. Kolekar, C. Nayak
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引用次数: 0
期刊
Indian Journal of Paediatric Dermatology
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