Shimasaki A K
Department of Internal Medicine, Himeji National Hospital.
Rinsho Ketsueki. 2001 Aug;42(8):639-43.
The syndrome of episodic angioedema associated with eosinophilia (EAE), originally identified by Gleich et al., is characterized by recurrent attacks of angioedema, urticaria, fever, increased body weight, and eosinophilia of unknown origin. Five young (aged 23-32 years) female patients were referred to our hospital because of eosinophilia (4,900-10,400/microliter). The chief complaints in all patients were angioedema and pain in the lower extremities without urticaria. Fever and increased body weight were not evident in most of the patients. These clinical features resolved spontaneously within 3 months, and no recurrence was observed. These characteristics were consistent with nonepisodic-type EAE (NEAE), which was proposed by Chikama et al. and is observed frequently in Japan. The clinical characteristics of NEAE were studied in the present 5 cases and the 25 cases reported previously in Japan. This revealed some additional characteristics: 1) a tendency for occurrence in autumn, 2) arthritis and absence of urticaria in some patients, and 3) increased serum LDH levels in some cases. It is suggested that NEAE should be treated with antiallergic drugs or simply followed without treatment, because spontaneous remission is observed frequently.
发作性血管性水肿伴嗜酸性粒细胞增多综合征(EAE)最初由格利希等人确定,其特征为血管性水肿、荨麻疹、发热、体重增加以及不明原因的嗜酸性粒细胞增多反复发作。五名年轻(年龄在23 - 32岁之间)女性患者因嗜酸性粒细胞增多(4900 - 10400/微升)被转诊至我院。所有患者的主要症状为血管性水肿和下肢疼痛,无荨麻疹。大多数患者无发热和体重增加。这些临床特征在3个月内自发缓解,未观察到复发。这些特征与Chikama等人提出的非发作型EAE(NEAE)一致,在日本较为常见。本研究对这5例患者以及日本此前报道的25例患者的NEAE临床特征进行了研究。结果发现了一些其他特征:1)秋季发病倾向;2)部分患者有关节炎且无荨麻疹;3)部分病例血清乳酸脱氢酶水平升高。建议对NEAE采用抗过敏药物治疗或仅进行观察而不治疗,因为经常会出现自发缓解。