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口服阿维A治疗播散性色素减退性角化病1例

A Case of Disseminated Hypopigmented Keratoses Improved with Oral Acitretin.

作者信息

Eskiocak Ali Haydar, Bassorgun Cumhur İbrahim, Uzun Sarp, Uzun Soner

机构信息

Department of Dermatology and Venereology, Akdeniz University School of Medicine Hospital, Antalya, Turkey.

Department of Pathology, Akdeniz University School of Medicine Hospital, Antalya, Turkey.

出版信息

Case Rep Dermatol Med. 2017;2017:1617375. doi: 10.1155/2017/1617375. Epub 2017 Dec 21.

Abstract

Disseminated hypopigmented keratosis is a distinct clinical entity and only few cases have been reported so far. Here, we present a 21-year-old man with almost 10-year history of hypopigmented, nonfollicular, keratotic lichenoid papules occurring on the extensor surfaces of the extremities, back and lumber region. Histopathological examination showed orthohyperkeratosis, irregular acanthosis, and sporadic papillomatosis with a normal amount of melanin and number of melanocytes. In addition, no marked inflammation or melanophages were seen. In order to exclude other possible causes, we performed laboratory tests and radiological examination which were all found to be normal. As the clinical and histopathological features of our patient were taken into account, it was considered to be compatible with the diagnosis of disseminated hypopigmented keratoses. So far, only topical therapies have been used with failure in the previously reported cases except one patient. Considering the extensive lesions, we treated the present patient with 5% salicylic acid in addition to oral acitretin and significant regression in all lesions was achieved, particularly on the keratosis.

摘要

播散性色素减退性角化病是一种独特的临床病症,迄今为止仅有少数病例报道。在此,我们报告一名21岁男性,其四肢伸侧、背部及腰部出现色素减退性、非毛囊性、角化性苔藓样丘疹近10年。组织病理学检查显示正角化过度、不规则棘层肥厚及散在乳头瘤样增生,黑色素含量及黑素细胞数量正常。此外,未见明显炎症或噬黑素细胞。为排除其他可能病因,我们进行了实验室检查及影像学检查,结果均正常。综合考虑患者的临床及组织病理学特征,认为符合播散性色素减退性角化病的诊断。迄今为止,除1例患者外,先前报道的病例仅采用局部治疗均告失败。鉴于皮损广泛,我们除给予患者口服阿维A外,还外用5%水杨酸治疗,所有皮损均显著消退,尤其是角化病损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a4/5752972/c62e0f19fdc5/CRIDM2017-1617375.001.jpg

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