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无毛发伴丘疹性皮损。

Atrichia with papular lesions.

作者信息

Bansal Manish, Manchanda Kajal, Lamba Sachin, Pandey Ss

机构信息

Departments of Dermatology and Venereology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.

出版信息

Int J Trichology. 2011 Jul;3(2):112-4. doi: 10.4103/0974-7753.90827.

Abstract

Atrichia with papular lesions (APL) is a rare autosomal recessive form of irreversible alopecia with onset at few months of age with papular keratin cysts over the body. It is associated with mutation in the Zinc finger domain of the human hairless gene on chromosome region 8p12. An eleven-year-old male presented with extensive alopecia starting at six months of age refractory to the treatment along with keratotic papules on the face and trunk. Biopsy from a papule showed mid-dermal keratin cysts and from the scalp showed few vellus follicles with no terminal hairs. The diagnosis of APL was made based upon the criteria proposed. Vitamin D-dependent rickets was ruled out as it has similar clinical presentation. Accurate diagnosis of APL is required to avoid unnecessary treatment to the patient as it is commonly misdiagnosed as alopecia universalis and treated with systemic steroids.

摘要

丘疹性皮损性无毛症(APL)是一种罕见的常染色体隐性遗传性不可逆脱发疾病,发病于几个月大时,全身出现丘疹性角质囊肿。它与8号染色体区域8p12上人类无毛基因的锌指结构域突变有关。一名11岁男性自6个月大时开始出现广泛性脱发,治疗无效,同时面部和躯干有角化丘疹。丘疹活检显示真皮中部角质囊肿,头皮活检显示有少量毳毛毛囊,无终毛。根据提出的标准诊断为APL。由于维生素D依赖性佝偻病有相似的临床表现,故排除了该病。需要准确诊断APL,以避免对患者进行不必要的治疗,因为它常被误诊为普秃并接受全身类固醇治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49d1/3250007/1cdee22cffd1/IJT-3-112-g001.jpg

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