A generalized rash in an 8-year-old patient

Ashley S. Kim, Astrid H. Lossius
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Abstract

An 8-year-old patient was referred for a second opinion to our dermatology department from another dermatologist. The referral reported a 14-month history of therapy-resistant rash, originally treated as nummular atopic dermatitis. The patient reported spontaneous debut of an itchy rash to the extremities and trunk, with worsening of symptoms despite use of topical steroids and UVB light therapy. The rash spread gradually to the entire body, including face and scalp. Upon examination, there was a polymorphic presentation with well-demarcated red macules, small subcorneal pustules along borders, patchy hyperkeratosis and postinflammatory hyperpigmentation (Figure 1a,b). The patient also had patchy hair thinning with a ‘black dot pattern’ (Figure 2). This finding resulted in diagnostic workup to exclude fungal infection, subacute cutaneous lupus, psoriasis and secondary syphilis, in order of decreasing clinical likelihood. Skin and hair samples were both positive for dermatophyte DNA, Trichophyton species. Histology also reported fungal elements in the keratin layer. Treatment initiated with terbinafine 125 mg daily for 6 weeks, in addition to ketoconazole shampoo. Upon control, the patient presented with postinflammatory hyperpigmentation, however, her other symptoms had abated and she had experienced hair regrowth. Control skin samples were negative for dermatophyte DNA.

Ashley S. Kim wrote the manuscript and Astrid H. Lossius provided revisions. Both authors were involved in the workup and final diagnosis of this patient. Ashley S. Kim is the corresponding author.

The authors declare no conflict of interest.

The parents of minor patients have been given written informed consent for their child's participation in this article, as well as for the use of their child's deidentified, anonymized case details (including photographs) for publication. Ethical approval: Not applicable.

Abstract Image

一名 8 岁患者的全身皮疹
一位 8 岁的患者从另一位皮肤科医生处转诊到我院皮肤科寻求第二诊疗意见。转诊者称其皮疹病史长达14个月,最初被当作麻疹性特应性皮炎治疗。患者自发出现四肢和躯干瘙痒性皮疹,尽管使用了局部类固醇激素和紫外线照射疗法,但症状仍不断恶化。皮疹逐渐蔓延至全身,包括面部和头皮。经检查,患者的皮疹呈多形性,伴有边界清楚的红色斑丘疹、角质层下沿边界的小脓疱、斑片状角化过度和炎症后色素沉着(图 1a、b)。患者还伴有斑片状头发稀疏,呈 "黑点模式"(图 2)。诊断结果显示,按照临床可能性递减的顺序,患者可能患有真菌感染、亚急性皮肤狼疮、银屑病和继发性梅毒。皮肤和头发样本中的皮癣菌 DNA(毛癣菌)均呈阳性。组织学检查也显示角质层中有真菌成分。治疗开始时,除了使用酮康唑洗发水外,还每天使用特比萘芬 125 毫克,持续 6 周。治疗结束后,患者出现了炎症后色素沉着,但其他症状有所缓解,头发也重新生长。对照组皮肤样本中的皮癣菌DNA呈阴性。Ashley S. Kim撰写了手稿,Astrid H. Lossius提供了修改意见。两位作者都参与了该患者的检查和最终诊断。作者声明无利益冲突。未成年患者的父母已书面知情同意其子女参与本文的写作,并同意将其子女的去标识化、匿名化病例细节(包括照片)用于发表。伦理批准:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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