Bagot M, Bagot J L, Besserman O, Bertrand J C
Rev Stomatol Chir Maxillofac. 1984;85(1):66-9.
A case of Gardner-Diamond's syndrome is reported in which the lesions were localized to the face. The syndrome is characterized by the spontaneous onset of recurrent painful ecchymoses mainly in young women. The elective site of the lesions is on the limbs, sometimes on the abdomen or thorax, and only rarely on the face. They are accompanied by a very rich symptomatology contrasting with normal biological test results. An autoerythrocytic sensitization mechanism has been suggested but few biological arguments exist to support this auto-immune hypothesis of its origin. In contrast, the psychological background is hysterical in type, and the affection can be included among the psychogenic purpuras.
报告了一例加德纳-戴蒙德综合征病例，其病变局限于面部。该综合征的特征是主要在年轻女性中自发出现反复发作的疼痛性瘀斑。病变的好发部位是四肢，有时在腹部或胸部，很少出现在面部。它们伴有丰富的症状，而生物学检查结果正常。有人提出了自身红细胞致敏机制，但几乎没有生物学依据支持其起源的自身免疫假说。相比之下，心理背景属于癔症类型，这种病症可归入心因性紫癜。
