|a,b,c,d)Clinical features of Galli–Galli disease, hyperpigmented slightly scaly papules|
Galli–Galli disease is a type of Dowling-Degos' disease, presenting with many small hard red-brown bumps 1mm to 2mm is size, laid out in a lace-like pattern. It typically occurs in flexures such as the underarms and neck, but also the arms, chest, hands, legs and groin.
The condition runs in families. The disease is also characterized by slowly progressive and disfiguring reticulate hyperpigmentation of the flexures, clinically and histopathologically diagnostic for Dowling-Degos disease but also associated with suprabasal, nondyskeratotic acantholysis.
It is rare.
- James, William D.; Elston, Dirk; Treat, James R.; Rosenbach, Misha A.; Neuhaus, Isaac (2020). "36. Disturbances of pigmentation: Galli–Galli disease". Andrews' Diseases of the Skin: Clinical Dermatology (13th ed.). Edinburgh: Elsevier. p. 866. ISBN 978-0-323-54753-6. Archived from the original on 2022-08-23. Retrieved 2022-08-12.
- Journal of the American Academy of Dermatology ISSN 0190-9622 CODEN JAADDB
- Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.