1. Lipoid proteinosis unveiled by oral mucosal lesions: a comprehensive analysis of 137 cases
- Author
-
Noam Yarom, Marilena Vered, Boaz Frenkel, and Shlomo Taicher
- Subjects
Adult ,Male ,Pathology ,medicine.medical_specialty ,Urbach–Wiethe disease ,Diagnosis, Differential ,Consanguinity ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Tongue ,Humans ,Medicine ,General Dentistry ,Hyaline ,business.industry ,Oral mucosal lesions ,030206 dentistry ,medicine.disease ,Dermatology ,stomatognathic diseases ,medicine.anatomical_structure ,Upper aerodigestive tract ,Lipoid Proteinosis of Urbach and Wiethe ,Female ,Mouth Diseases ,business ,SKIN SCARRING ,Lesion site ,Labial lesions - Abstract
Lipoid proteinosis (LP) is a rare autosomal recessive disorder characterized by deposits of hyaline material within skin and mucous membranes of the upper aerodigestive tract, especially the vocal cords. We aimed to investigate possible associations between oral LP (oLP) manifestations and demographic data and extra-oral lesions. Cases of oLP were collected following a systematic search of Medline’s PubMed and Google Scholar (1948–2014). We added four new cases. Demographic data, consanguineous marriage status, oral lesion site(s), and related symptoms were analyzed for potential associations. A total of 137 patients with oLP lesions were analyzed. Parental consanguinity status was known for 52 patients, and the parents were not related in 38 (73%) of them. The tongue was the most commonly affected oral site (68%), and it was associated with significantly more affected family members (P = 0.002). The palate and gingiva were the least involved sites (25 and 6%, respectively): the former had a tendency to be affected in younger patients and the latter in older ones. Patients with palatal and labial lesions had significantly less skin scarring (P
- Published
- 2016
- Full Text
- View/download PDF