Dermal acquired melanocytosis D22.-

Last updated on: 30.04.2025

Dieser Artikel auf Deutsch

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.

Benign, blue to blue-grey spots or patches that usually only become noticeable at the age of 30 or 40 and are histologically characterized by a proliferation of dermal, pigmented, spindle and/or dendritic cells. Acquired dermal melanocytosis occurs predominantly in the Asian population.

ClassificationThis section has been translated automatically.

The following subdivision can be made according to their distribution pattern:

  • Facially localized acquired dermal melanocytosis (w>m)
  • Extrafacially localized acquired dermal melanocytosis (m>w)

EtiopathogenesisThis section has been translated automatically.

Unknown. Genetic predisposition likely; people of Asian origin are more frequently affected. Reactivation of already latent melanocytes (Grimaux X et al. 2020)?

ClinicThis section has been translated automatically.

Facial, acquired dermal melanocytosis is similar to nevus ota. There are blurred, asymptomatic, brown patches of different colors, 2.0-5.0 cm in size, with normal hair.

The extrafacial, acquired dermal melanocytoses are similar to nevus Ito and are predominantly found on the trunk. There are blurred, asymptomatic, brown patches of varying color, 3.0-10.0 cm in size, with normal hair.

HistologyThis section has been translated automatically.

Histology: Loosely distributed S100+, MelanA+, HMB45+ and SOX10+ cells in the upper and middle dermis. No inflammatory infiltrates. The epidermis shows a normal distribution of melanocytes.

Progression/forecastThis section has been translated automatically.

Benign! There is no tendency to regression.

LiteratureThis section has been translated automatically.

  1. Baroody M, Holds JB (2004) Extensive locoregional malignant melanoma transformation in a patient with oculodermal melanocytosis. Plast Reconstr Surg 113: 317-322.
  2. Goncharuk V et al. (2003) Bednar tumor associated with dermal melanocytosis: melanocytic colonization or neuroectodermal multidirectional differentiation? J Cutan Pathol 30: 147-151.
  3. Grimaux X et al. (2020) An unusual brownish patch on the back of a 74-year-old Caucasian man. J Dtsch Dermatol Ges 18:638-640.
  4. Hanson M et al. (2003) Association of dermal melanocytosis with lysosomal storage disease: clinical features and hypotheses regarding pathogenesis. Arch Dermatol 139: 916-920
  5. Hyun DJ et al. (2016) Acquired dermal melanocytosis occurring in a patient with hyophidrotic ectodermal dysplasia. Ann Dermatol 28: 785-787
  6. Rubin AI et al. (2001) Acquired dermal melanocytosis: appearance during pregnancy. J Am Acad Dermatol 45: 609-613

Last updated on: 30.04.2025