Galli–Galli disease

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Galli–Galli disease
PMC4150463 bjd0170-1362-f1.png
a,b,c,d)Clinical features of Galli–Galli disease, hyperpigmented slightly scaly papules
SpecialtyDermatology
FrequencyRare[1]

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.[1] It typically occurs in flexures 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. 1.0 1.1 1.2 1.3 1.4 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.
  2. Journal of the American Academy of Dermatology ISSN 0190-9622 CODEN JAADDB
  3. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.