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Galli–Galli disease
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Galli–Galli disease : ウィキペディア英語版
Galli–Galli disease
Galli–Galli disease is a rare inherited condition that has close resemblance clinically to Dowling-Degos' disease, but is histologically distinct, characterized by skin lesions that are 1- to 2-mm slightly keratotic red to dark brown papules which are focally confluent in a reticulate pattern.〔James, William; Berger, Timothy; Elston, Dirk ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.〕 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.〔Journal of the American Academy of Dermatology ISSN 0190-9622 CODEN JAADDB〕
==See also==

* List of cutaneous conditions

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Galli–Galli disease」の詳細全文を読む



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