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El Shabrawi-Caelen, L; Rütten, A; Kerl, H.
The expanding spectrum of Galli-Galli disease.
J Am Acad Dermatol. 2007; 56(5 Suppl):S86-S91 Doi: 10.1016/j.jaad.2006.10.987 (- Case Report)
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Führende Autor*innen der Med Uni Graz
El-Shabrawi-Caelen Laila
Co-Autor*innen der Med Uni Graz
Kerl Helmut
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Abstract:
Galli-Galli disease (GGD), a rare genodermatosis in the spectrum of reticulate hyperpigmentation, is regarded as an acantholytic variant of Dowling-Degos disease. We herein report two patients with GGD exhibiting erythematous scaly plaques and lentigo-like macules on the trunk and lower extremities, rather than the characteristic reticulate hyperpigmented macules of large body folds. Digitate elongations of rete ridges coupled with foci of acantholysis were the clues to the diagnosis. A high index of suspicion is needed to diagnose GGD that lacks the characteristic reticulate hyperpigmentation of large body folds.
Find related publications in this database (using NLM MeSH Indexing)
Acantholysis - etiology Acantholysis - pathology
Aged -
Chromosomes, Human, Pair 12 -
Diagnosis, Differential -
Female -
Genes, Dominant -
Humans -
Keratin-5 - genetics
Mutation -
Pigmentation Disorders - complications Pigmentation Disorders - diagnosis Pigmentation Disorders - genetics Pigmentation Disorders - pathology
Skin - pathology

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