Kleiner-Baumgarten A, Schlaeffer F, Keynan A
Arch Intern Med. 1983 Oct;143(10):1987-9.
Idiopathic thrombocytopenic purpura developed in a 31-year-old man, and he underwent a splenectomy because of his failure to respond to steroid therapy. Subsequently, during a six-year follow-up, chronic active hepatitis, Coombs' positive hemolytic anemia, and pulmonary interstitial fibrosis developed. Since such a clustering of autoimmune manifestations in a single subject is unusual, possible contributing factors were sought. We suggest that both the splenectomy and the histocompatibility antigen HLA-B8, which the patient was found to carry, may have contributed to this rare clinical syndrome.
一名31岁男性患特发性血小板减少性紫癜,因对类固醇治疗无反应而接受了脾切除术。随后,在六年的随访期间,出现了慢性活动性肝炎、库姆斯试验阳性的溶血性贫血和肺间质纤维化。由于单一受试者出现这种自身免疫表现的聚集情况并不常见,因此寻找了可能的促成因素。我们认为脾切除术以及该患者被发现携带的组织相容性抗原HLA - B8可能都促成了这种罕见的临床综合征。