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Jalil, A. A. and Zain, R. B. and van der Waal, I. (2005) Darier disease: a case report. British Journal of Oral and Maxillofacial Surgery, 43 (4). pp. 336-338. ISSN 0266-4356

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    Abstract

    Darier disease, also known as keratosis follicularis, dyskeratosis follicularis, and benign dyskeratosis, is a rare disorder of keratinisation that primarily affects the skin and, to a lesser extent, the oral mucosa. It was described independently by both Darier and White in 1889. It has a prevalence of 1:100,000 of the population and is inherited as an autosomal dominant trait.1 The age of onset is childhood or adolescence. Patients usually present with multiple small firm reddish-brown papules on the forehead, scalp, neck, shoulders, chest, and limbs. Other cutaneous signs include punctate keratotic pits of the palms and soles and dystrophy of the nails, which is characterised by a red and white sandwich of streaks associated with a V-shaped notch. The oral lesions are usually asymptomatic and are seen as multiple, normal-coloured or white flat-topped papules that predominantly affect the palate.

    Item Type: Article
    Uncontrolled Keywords: Benign Dyskeratosis, Darier Disease, Dyskeratosis Follicularis, Keratosis Follicularis, Oral Squamous Cell Carcinoma, OSCC, Lichenoid Lesions, Lichen Planus, Oral Cancer, Oral Tumours, Pemphigus, Traumatic Eosinophilic Pranuloma, Aphthous Ulcers, Oral Mucosal Lesions, Betel Chewers Mucosa, Betel Quid Related Lesions, Betel Quid, Areca Quid, Tobacco Quid, Oral Cancer Screening, Training and Calibration, Early Detection, Oral Cancer Awareness, Biobanking, Tissue Bank, Databank, Oral Cancer, Tissue Bank, Research Credibility, Research Ethics.
    Subjects: Medicine and Dentistry
    Divisions: UNSPECIFIED
    Depositing User: Prof. Dr. Rosnah Mohd Zain
    Date Deposited: 02 Feb 2012 00:54
    Last Modified: 02 Feb 2012 00:54
    URI: http://opendepot.org/id/eprint/607

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