Abstract:
:Galli-Galli disease (GGD) and Dowling-Degos disease (DDD) are inherited skin diseases with variable progressive course. They are of benign and harmless behaviour but aesthetically annoying. They are subsumed within the group of reticulate pigmented disorders of the skin to which, additionally, Kitamura's and Haber's diseases are counted. Clinical appearance is approximately similar, with slight differences in age of onset and associated disorders. Histopathological features are almost similar aside from the unique hallmark of suprabasal acantholysis, which can exclusively be observed in GGD. We report four typical cases of reticulate pigmented disorders, clinically accordable to DDD but histopathologically allocated to GGD. In conclusion, we purpose the idea of a wide spectrum of reticulate pigmented disorders in which Morbus Galli-Galli should probably be reclassified as a subset of DDD.
journal_name
J Cutan Patholjournal_title
Journal of cutaneous pathologyauthors
Müller CS,Pföhler C,Tilgen Wdoi
10.1111/j.1600-0560.2008.00995.xsubject
Has Abstractpub_date
2009-01-01 00:00:00pages
44-8issue
1eissn
0303-6987issn
1600-0560pii
CUP995journal_volume
36pub_type
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