Clark G D, Key J D, Rutherford P, Bithoney W G
Pediatrics. 1984 Dec;74(6):1100-2.
Munchausen's syndrome was initially described in 1951. It has become increasingly recognized since that time. Recently, Munchausen's syndrome by proxy or Polle syndrome has been described. In this disease entity, a parent causes a factitious disease in a child. The disease may require extensive medical testing and the result may even be death. A wide variety of presentations of Polle syndrome have been reported including cardiac arrest, recurrent sepsis, and factitious bleeding. Autoerythrocyte sensitization, a syndrome of spontaneous purpura, was initially described in 1955. The diagnostic test described is intradermal injection of autologous blood which produces an area of painful purpura. The syndrome is therefore postulated to be due to hypersensitivity in the patient's own RBCs. The majority of patients with autoerythrocyte sensitization have had psychiatric disorders and the symptoms have improved only with psychotherapy. An infant who had a clinical picture of autoerythrocyte sensitization and who was later found to be a victim of Polle syndrome is reported.
孟乔森综合征于1951年首次被描述。自那时起,它越来越受到人们的认识。最近,代理型孟乔森综合征或波利综合征被描述出来。在这种疾病实体中,父母会在孩子身上引发一种人为疾病。这种疾病可能需要进行广泛的医学检查,结果甚至可能是死亡。已经报道了波利综合征的多种表现形式,包括心脏骤停、复发性败血症和人为出血。自体红细胞致敏是一种自发性紫癜综合征,于1955年首次被描述。所描述的诊断测试是皮内注射自体血液,这会产生一个疼痛性紫癜区域。因此,推测该综合征是由于患者自身红细胞的超敏反应所致。大多数自体红细胞致敏患者患有精神疾病,症状仅通过心理治疗得到改善。本文报道了一名具有自体红细胞致敏临床表现的婴儿,该婴儿后来被发现是波利综合征的受害者。