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Galli-Galli disease: an unrecognized entity or an acantholytic variant of Dowling-Degos disease?

Abstract：

:Galli-Galli disease is an inherited disease 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. A few patients exhibiting these features have been described, mainly in the non-English-language literature, which suggests that Galli-Galli disease is not an entity of its own, as originally thought, but is an acantholytic variant of Dowling-Degos disease. We report a typical case of Galli-Galli disease, which supports this concept.

journal_name

J Am Acad Dermatol

journal_title

Journal of the American Academy of Dermatology

authors

Braun-Falco M,Volgger W,Borelli S,Ring J,Disch R

doi

10.1067/mjd.2001.116340

subject

Has Abstract

pub_date

2001-11-01 00:00:00

pages

760-3

issue

5

eissn

0190-9622

issn

1097-6787

pii

S0190-9622(01)33978-6

journal_volume

45

pub_type

杂志文章

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