Mota R, Reifenberger J, Hanneken S, Mühlenstädt E
Hautklinik des Universitätsklinikums Düsseldorf, Düsseldorf.
Hautarzt. 2010 Apr;61(4):284-6. doi: 10.1007/s00105-010-1936-5.
Galli-Galli disease is a rare genodermatosis which classically presents with reticulate hyperpigmentation of the flexures and intertriginous areas. Recently, an atypical clinical presentation of Galli-Galli disease with monomorphic lentigo-like maculae and papules has been reported. We describe two cases of Galli-Galli disease, one patient presenting with a classical form and another with atypical skin lesions. In spite of the clinical differences, the histopathological examination - with filiform elongated rete ridges and acantholysis - confirmed the diagnosis of Galli-Galli disease in both cases.
加利-加利病是一种罕见的遗传性皮肤病,典型表现为屈侧和间擦部位的网状色素沉着。最近,有报道称加利-加利病出现了非典型临床表现,表现为单形性雀斑样斑疹和丘疹。我们描述了两例加利-加利病病例,一例表现为经典形式,另一例有非典型皮肤损害。尽管临床表现不同,但组织病理学检查——丝状延长的 rete 嵴和棘层松解——证实两例均为加利-加利病。