Ceuppens J L, Stevens E, Fevery J, Schurmans J
Gastroenterology. 1984 May;86(5 Pt 1):937-40.
A 17-yr-old woman presented with acute hepatitis B. She had preexisting well-documented immune deficiency, clinically apparent as chronic mucocutaneous candidiasis, and recurrent severe viral infections. Life-threatening but spontaneously resolving Coombs-negative hemolysis complicated the recovery phase. Complete healing of the hepatitis with disappearance of hepatitis B surface antigen from serum and normal hepatitis B surface antibody and hepatitis B core antibody production occurred in spite of T-cell dysfunction.
一名17岁女性出现急性乙型肝炎。她先前有充分记录的免疫缺陷,临床上表现为慢性黏膜皮肤念珠菌病以及反复发生的严重病毒感染。在恢复阶段出现了危及生命但可自发缓解的抗人球蛋白试验阴性溶血。尽管存在T细胞功能障碍,但肝炎完全愈合,血清中乙型肝炎表面抗原消失,乙型肝炎表面抗体和乙型肝炎核心抗体产生正常。