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重症皮质类固醇治疗的隐源性慢性活动性肝炎的临床特征及预后意义

Clinical features and prognostic implications of severe corticosteroid-treated cryptogenic chronic active hepatitis.

作者信息

Czaja A J, Hay J E, Rakela J

机构信息

Division of Gastroenterology, Mayo Clinic, Rochester, MN 55905.

出版信息

Mayo Clin Proc. 1990 Jan;65(1):23-30. doi: 10.1016/s0025-6196(12)62106-5.

DOI:10.1016/s0025-6196(12)62106-5
PMID:2296210
Abstract

To assess the nature and prognosis of severe chronic active hepatitis of unknown cause, we compared 26 patients who had been fully screened for etiologic factors with 112 patients who had autoimmune chronic active hepatitis after similar durations of corticosteroid therapy (17(+)/- 2 versus 23 (+)/- 2 months), and follow-up versus 103 +/- 7 months). Patients with cryptogenic disease could not be distinguished from those with autoimmune disease on the basis of age, sex distribution, duration of illness, immunoglobulin levels, frequency of concurrent immunologic disorders, or histologic findings. Serum gamma-globulin levels were higher (3.4 +/- 0.1 versus 2.5 +/- 0.2 g/dl, P = 0.007) and albumin levels were lower (2.9 +/- 0.1 versus 3.3 +/- 0.1 g/dl, P = 0.003) in patients with autoimmune disease than in those with cryptogenic disease, but individual findings did not differentiate the patients. Remission (69 versus 75%), treatment failure (23 versus 13%), relapse after drug withdrawal (67 versus 68%), progression to cirrhosis (57 versus 36%), and death from hepatic failure (12 versus 11%) occurred as commonly in patients with cryptogenic as in those with autoimmune disease. Patients with different constellations of immunoserologic findings were similar clinically. We conclude that patients with severe chronic active hepatitis who have been fully screened for etiologic factors cannot be distinguished from patients with autoimmune disease of comparable severity. These two groups of patients have a similar prognosis after corticosteroid therapy, and such treatment should be considered in these highly selected patients.

摘要

为评估病因不明的重度慢性活动性肝炎的性质及预后,我们将26例已全面筛查病因的患者与112例自身免疫性慢性活动性肝炎患者进行了比较,这些患者接受了相似疗程的皮质类固醇治疗(分别为17(±)/ - 2个月与23(±)/ - 2个月),随访时间分别为103±7个月与103±7个月。隐源性疾病患者在年龄、性别分布、病程、免疫球蛋白水平、并发免疫紊乱的频率或组织学表现方面,与自身免疫性疾病患者并无差异。自身免疫性疾病患者的血清γ-球蛋白水平较高(3.4±0.1与2.5±0.2g/dl,P = 0.007),白蛋白水平较低(2.9±0.1与3.3±0.1g/dl,P = 0.003),但个体检查结果并不能区分这些患者。隐源性疾病患者与自身免疫性疾病患者出现缓解(分别为69%与75%)、治疗失败(分别为23%与13%)、停药后复发(分别为67%与68%)、进展为肝硬化(分别为57%与36%)以及死于肝衰竭(分别为12%与11%)的情况相当常见。具有不同免疫血清学表现组合的患者在临床上相似。我们得出结论,已全面筛查病因的重度慢性活动性肝炎患者与具有相当严重程度的自身免疫性疾病患者无法区分。这两组患者在皮质类固醇治疗后的预后相似,对于这些经过严格筛选的患者应考虑进行此类治疗。

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