DepigmentationL81.8

Author:Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 29.10.2020

Dieser Artikel auf Deutsch

Synonym(s)

Depigmentations; Hypomelanosis; Hypomelanosis (e); Hypopigmentation; Lack of Pigment; Light skin; Loss of pigment; macules; Pigment deficiency; Skin spots; Variations in pigmentation; White patches of skin

Requires free registration (medical professionals only)

Please login to access all articles, images, and functions.

Our content is available exclusively to medical professionals. If you have already registered, please login. If you haven't, you can register for free (medical professionals only).


Requires free registration (medical professionals only)

Please complete your registration to access all articles and images.

To gain access, you must complete your registration. You either haven't confirmed your e-mail address or we still need proof that you are a member of the medical profession.

Finish your registration now

DefinitionThis section has been translated automatically.

Depigmentation is a pathological, clinical symptom caused by a congenital or acquired, solitary or multiple, localized or disseminated, in rare cases also generalized or universal color loss of the skin, caused by a melanin deficiency(hypomelanosis) or by a complete melanin loss(amelanosis) of the skin due to loss or dysfunction of melanocytes. If depigmentation or hypopigmentation occurs temporarily as a result of skin diseases (intra- and/or perilesional), they are called leukoderms, s.a. pseudoleukoderm.

Depigmentation is the opposite pathological finding of hyperpigmentation.

ClassificationThis section has been translated automatically.

In the following, clinical pictures are listed which are characterized by the clinical symptom "depigmentation".

EtiopathogenesisThis section has been translated automatically.

It is already assumed that > 100 genes are involved in skin pigmentation. Disturbances can occur at any level of pigmentation due to:
  • Change in melanocyte count
  • inadequate melanin synthesis
  • defects in the maturation, transport or transfer of melanosomes

Note(s)This section has been translated automatically.

The opposite finding, the pathological compression of the melanin of the skin or mucous membrane, is called hyperpigmentation.

LiteratureThis section has been translated automatically.

  1. Giehl K et al (2010) Genetically caused pigmentation disorders. Dermatologist 61: 567-577

Authors

Last updated on: 29.10.2020