Galli–Galli disease
| Galli–Galli disease | |
|---|---|
 | |
| Clinical features of Galli–Galli disease, hyperpigmented slightly scaly papules | |
 | |
| Specialty | Dermatology |
| Frequency | Rare[1] |
Galli–Galli disease is a type of Dowling-Degos' disease, a reticulate pigmentary disorder.[1] It presents with many small hard red-brown bumps 1mm to 2mm is size, laid out in a lace-like pattern.[1] These typically occur in skin folds such as the underarms and neck, but also the arms, chest, hands, legs and groin.[1]
The condition runs in families.[1] 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.[2][3]
It is rare.[1]
See also
References
- 1 2 3 4 5 6 James, William D.; Elston, Dirk; Treat, James R.; Rosenbach, Misha A.; Neuhaus, Isaac (2020). "36. Disturbances of pigmentation". Andrews' Diseases of the Skin: Clinical Dermatology (13th ed.). Edinburgh: Elsevier. p. 866. ISBN 978-0-323-54753-6. Archived from the original on 2023-06-30. Retrieved 2023-05-05.
- ↑ 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.
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