The skin is colored by a blend of pigments, which form part of a complex and highly regulated process. Pigmentary defects normally present with dyschromia and can be caused by genetic defects, systemic disease, inflammatory processes, metabolic defects, infections, tumors, or toxic or iatrogenic causes.
This atlas is an extensive text written by key opinion leaders within dermatology, it has a comprehensive format that guides the reader through the epidemiology, pathophysiology, diagnosis, treatment, and differential diagnosis of both common and rare pigmentary disorders. It illustrates the diagnosis and recognition of pigmentary disorders with a wide range of images.
İçerik tablosu
The mechanisms of pigmentation.- Acquired hypermelanosis.- Genetic hypermelanosis.- Acquired hypomelanosis.- Genetic hypomelanosis.- Non-melanic pigmentary disorders.- Drug-induced discoloration.- Nail discoloration.
Yazar hakkında
Thierry Passeron, MD, Ph D, is a Professor of Dermatology at the University of Hospital of Nice, France.
After his medical training Professor Passeron specialized in Dermatology in Nice University Hospital. From 2005 to 2007, he worked in the laboratory of Dr Vincent J Hearing at the National Institute of Health, National Cancer Institute, Bethesda, US, and characterized the role of SOX9 in melanocytes and in melanoma. Since 2010, he is full Professor of Dermatology at the University Hospital of Nice, France. Professor Passeron also heads the laboratory INSERM U1065 team 12, C3M, dedicated to the study of molecular mechanisms involved in pigmentation and melanoma and the University laser center. Currently, he has four international patents and more than 150 publications in scientific journals (h-index 30). His fields of research include pigmentary disorders, melanoma, and lasers.
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