Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders

• Main Authors: H. Alshaikh, F. Alsaif, S. Aldukhi
• Format: Article
• Language: English
• Published: Hindawi Limited 2017-01-01
• Series: Dermatology Research and Practice
• Online Access: http://dx.doi.org/10.1155/2017/3518568

Reticulated pigmentation is a unique pigmentary change caused by a heterogeneous group of hereditary and acquired disorders. This pigmentation is characterized by a mottled appearance, with lesions that vary in size and pigmentary content. This review discusses the hereditary group of the reticulated pigmentation disorders, such as dyschromatosis symmetrica hereditaria, dyschromatosis universalis hereditaria, and reticulate acropigmentation of Kitamura. The clinical presentation and histopathological features often overlap, making diagnosis difficult. However, each of these hereditary conditions possesses a unique genetic mutation, and genetic analysis is thus more useful in the diagnosis of these conditions. This article delivers an update regarding the clinical features, detailed histopathological description, and genetic information concerning hereditary reticulate pigmentary disorders and aims to provide useful background for use by clinical dermatologists and histopathologists when approaching this group of hereditary disorders.