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Behcet病是以口、眼和生殖器溃疡为特征的综合征。本病合并肝损害尚未引起注意,我们从1973年以来共见到4例,均为男性,年龄24~48岁;病程8月~28年。均有典型皮肤、口腔粘膜、眼、生殖器病变及间竭低热,均经皮肤活检确诊。3例有肝脏肿大(肋下1~2cm);4例均有SGPT升高和/或浊度试验阳性,两例高热呈败血症样表现者且有黄疸(Ⅱ分别为36、56u);HBsAg均为阴性。2例经激素治疗后康复,另2例败血症样患者则黄疸及SGPT持续升高,并消化道出血、休克、昏迷而死亡。
Behcet’s disease is a syndrome characterized by mouth, eye and genital ulcers. The disease with liver damage has not attracted attention, we have seen since 1973, four cases were male, aged 24 to 48 years; duration of August to 28 years. Have a typical skin, oral mucosa, eye, genital lesions and exhaustive fever, are diagnosed by skin biopsy. 3 cases had enlargement of the liver (1 ~ 2 cm below the ribs); 4 cases had positive SGPT and / or turbidity test, 2 cases showed high fever sepsis-like and jaundice (Ⅱ, 36,56u respectively); HBsAg All negative. 2 patients recovered after hormone therapy, and the other 2 patients with sepsis-like jaundice and SGPT continued to rise, and gastrointestinal bleeding, shock, coma and death.