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白塞氏病是一种多系统损害的血管炎性疾病,临床上不常见。现报道一例如下: 患者女性,41岁。于入院前三天突然感到阴部搔痒不止,次日因阴部疼痛,同时伴有口腔粘膜溃疡及双眼结膜充血而就诊入院。平素身体健康,但一年前曾有类似发作史。体温36.4℃,营养发育正常,全身皮肤无(疒节)肿及丘疹,右手背皮肤可见多形性红斑。头颅正常,双眼结膜充血明显,口唇、舌缘及两颊粘膜均有溃疡。心肺听诊阴性,肝脾不肿大,四肢关节活动佳,神经系统检查无异常。妇科检查:外阴充血,大小阴唇多处溃疡,阴道内有溃疡。ESR34mm,粘蛋白89.5％(以蛋白计)。蛋白电泳正常。胸透阴性,EKG为窦性心律。入院后给予激素、维生素及免疫抑制剂等治疗,锡类散
Behcet’s disease is a multi-systemic vascular disease that is not clinically common. A report is as follows: Female patient, 41 years old. Three days before admission suddenly felt genital itching more than the next day due to genital pain, accompanied by oral mucosal ulceration and conjunctival hyperemia and hospital admission. Usually healthy, but a year ago there was a history of similar attacks. Body temperature 36.4 ℃, normal vegetative development, systemic skin without (tarsal) swelling and papules, right-sided skin visible erythema multiforme. Normal skull, conjunctival hyperemia, lips, tongue edge and both buccal mucosa ulcers. Cardiopulmonary auscultation negative, liver and spleen is not enlarged, good joint activity, nervous system examination was normal. Gynecological examination: vulva congestion, multiple size labia ulcers, ulcers in the vagina. ESR 34mm, Mucin 89.5% (based on protein). Protein electrophoresis normal. Thoracotomy negative, EKG sinus rhythm. After admission to give hormones, vitamins and immunosuppressive agents and other treatment, tin scattered