Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3188581 | Annales de Dermatologie et de Vénéréologie | 2011 | 4 Pages |
Abstract
ALA is a rare and poorly understood condition. Based on the ten or so case reports in the literature, we attempted to define the clinical and histological profile of the disease as well as its course and its relationship with other forms of atrophic panniculitis. In particular, the onset of LAC in our patient presenting several autoimmune diseases underlines its close relationship to the condition described as “connective tissue panniculitis”.
Keywords
Related Topics
Health Sciences
Medicine and Dentistry
Dermatology
Authors
Z. Lamam Bennani, L. Boussofara, M. Denguezli, N. Ghariani, W. Saidi, B. Sriha, C. Belajouza, R. Nouira,