Full Description
There are many disorders of a lack of pigmentation in the skin, with different causations
and effects, of which vitiligo is only the best known; this comprehensive text from international
experts will enable clinicians to diagnose the full range of these conditions and suggest
the most effective management options for their patients.
Contents: Basic concepts of melanocyte biology * Approach to hypopigmentation *
Historical review of vitiligo * Epidemiology and classification of vitiligo * Pathophysiology
of vitiligo * Segmental vitiligo * Childhood versus post-childhood vitiligo * Pharmacological
therapy of vitiligo * Surgical treatment of vitiligo * Phototherapy and lasers in the treatment
of vitiligo * Emerging treatments for vitiligo * Tuberous sclerosis complex * Oculocutaneous
albinism * Hermansky-Pudlak syndrome, Chediak-Chigasi syndrome, and Griscelli
syndrome * Piebaldism * Waardenburg syndrome * Alezzandrini syndrome, Margolis
syndrome, Cross syndrome, and other rare genetic disorders * Mosaic hypopigmentation
* Skin disorders causing post-inflammatory hypopigmentation * Infectious and parasitic
causes of hypopigmentation * Melanoma leukoderma * Halo nevi * Drug-induced hypopigmentation
* Hypopigmentation from chemical and physical agents * Guttate hypomelanosis
and progressive hypomelanosis of the trunk (progressive macular hypomelanosis)
Contents
1. Basic concepts of melanocyte biology. 2. Approach to hypopigmentation. 3. Historical review of vitiligo. 4. Epidemiology and classification of vitiligo. 5. Pathophysiology of vitiligo. 6. Segmental vitiligo. 7. Childhood versus post-childhood vitiligo. 8. Pharmacological therapy of vitiligo. 9. Surgical treatment of vitiligo. 10. Phototherapy and lasers in the treatment of vitiligo. 11. Emerging treatments for vitiligo. 12. Tuberous sclerosis complex. 13. Oculocutaneous albinism. 14. Hermansky-Pudlak syndrome, Chediak-Chigasi syndrome, and Griscelli syndrome. 15. Piebaldism. 16. Waardenburg syndrome. 17. Alezzandrini syndrome, Margolis syndrome, Cross syndrome, and other rare genetic disorders. 18. Mosaic hypopigmentation. 19. Skin disorders causing post-inflammatory hypopigmentation. 20. Infectious and parasitic causes of hypopigmentation. 21. Melanoma leukoderma. 22. Halo nevi. 23. Drug-induced hypopigmentation. 24. Hypopigmentation from chemical and physical agents. 25. Guttate hypomelanosis and progressive hypomelanosis of the trunk (progressive macular hypomelanosis).
