Progressive macular hypomelanosis of the trunk: primary acquired hypopigmentation
- 1 October 1988
- journal article
- research article
- Published by Wiley in Journal of Cutaneous Pathology
- Vol. 15 (5) , 286-289
- https://doi.org/10.1111/j.1600-0560.1988.tb00561.x
Abstract
Dermatological practice in Martinique [West Indies] frequently encounters a bizarre skin condition presenting as a progressive and extensive hypomelanosis on the back. The course of this disorder is highly characteristic: it occurs mainly in females from 18-25 years of age, with a progressive development of round, pale, coalescent macules on the back and sometimes on the abdomen. This disease, which does not respond to therapy, spontaneously regresses within 3 to 4 years. Decreased epidermal melanin is the only histological feature. Ultrastructural examination of two cases found that the macular lesions were characterized by a switch from Stage IV single melanosomes (negroid) to small Type I-III aggregated melanosomes (caucasoid). It may thus be stated that the variation in skin coloration in these patients was due to a variation in melanosome size and distribution.This publication has 8 references indexed in Scilit:
- Vitiligo and Other Hypomelanoses of Hair and SkinPublished by Springer Nature ,1983
- Lack of evidence that inactivation of the mouse X-chromosome is incompleteGenetics Research, 1966
- Erythema dyschromicum perstans. (Ashy dermatosis)Archives of Dermatology, 1966
- Idiopathic guttate hypomelanosisArchives of Dermatology, 1966
- SEX CHROMATIN AND GENE ACTION IN MAMMALIAN X-CHROMOSOME1962
- Erythema Dyschromicum PerstansJournal of Investigative Dermatology, 1961