Department of Demoto-Venereology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 40016 China.
Dermatol Ther (Heidelb). 2012 Dec;2(1):5. doi: 10.1007/s13555-012-0005-7. Epub 2012 Apr 17.
Autoerythrocyte sensitization syndrome (AES) is a disorder characterized by recurrent, spontaneous, painful bruising in patients with underlying psychosis and neurosis. Its pathogenesis is uncertain. Purpuric lesions reproduced by injections of washed autologous erythrocytes suggest an autoimmune etiology. The authors described a 50-year-old woman who presented with recurrent episodes of painful bruising for 8 months, along with a 2-year history of general chronic neurodermatitis. A diagnosis of AES was made on the basis of the clinical symptoms and laboratory examinations results: the positive autoerythrocyte sensitization test and psychophysiologic derangement. However, the noticeable symptoms, simultaneously identical distribution of the ecchymosis and neurodermatitis lesions, as well as concomitant symptom of itching over the ecchymosis, created doubts regarding the real etiopathogenesis of the ecchymosis and whether the ecchymosis in the present patient were just factitious purpura. The authors discuss the rarity of this case, which to the authors' knowledge, had not been previously reported in the literature.
自身红细胞致敏综合征(AES)是一种以反复、自发性、疼痛性瘀斑为特征的疾病,发生于潜在的精神病和神经症患者。其发病机制尚不清楚。用自身洗涤红细胞注射复制出的紫癜性病变提示自身免疫病因。作者描述了一位 50 岁女性,她反复出现疼痛性瘀斑 8 个月,同时伴有 2 年的慢性全身性神经皮炎病史。根据临床症状和实验室检查结果,诊断为 AES:自身红细胞致敏试验阳性和精神生理障碍。然而,显著的症状、瘀斑和神经皮炎病变的同时相同分布,以及瘀斑上瘙痒的伴随症状,对瘀斑的真正病因和该患者的瘀斑是否只是人为性紫癜产生了疑问。作者讨论了该病例的罕见性,据作者所知,该病例以前在文献中尚未报道过。