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Neuro-Behcet's Syndrome: A Case Report

机译：Neuro-Behcet综合征：一例报告

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We report a case fulfilling the diagnostic criteria of Behçet's disease (BD) with a intracerebral hemorrhage who improve from this cerebrovascular complication and remained free of BD's activity for more than two years after be treated traditionally. The authors believe it is an anecdotic report but herbal medicines probable can be useful in the management of some patients with this condition. Introduction Something very similar to the current process known as Beh?et's disease (BD), Adamantiades-Beh?et's Syndrome, Halushi-Beh?ect's Syndrome, Oculo-Bucco-Genital Syndrome, Touraine's Aphthosis, or Triple Symptom complex of Beh?et was described by Hypocrates centuries ago and probably not by coincidence it was re-described in a ten years period by a Turkish dermatologist Hulussi Beh?et in 1937. Most of the confirmed patients have been identify along the ancient Silk Road which extend from Eastern Asia and Middle East to the Mediterranean basin,1 and most of the papers presented on the 10th International Congress on Beh?et's Disease held in Berlin during June 27-29, 2002 based on epidemiology, reported a higher prevalence of BD in those mentioned countries2. Epidemiological findings suggest that both genetic and environmental factors influence the pathogenesis of the disease. BD is a rare and chronic condition of unknown cause that affects in young peoples the inner lining of the mouth and genitals and the small blood vessels all over the body including eyes and brain among others system, causing recurring mouth and genital ulcers; those sores can occur in the tongue, and on the inside of the lips and cheeks usually lasting for one to three weeks, the genital ulcers appear less often than the mouth sores and they are sometimes mistaken for herpetic lesions; skin involvement is also common. Uveitis and retinitis causing blindness can be present, also arthritis, peripheral vasculitis and neurological complications often called Neuro-Beh?et's Syndrome (NBS). Clinical criteria for the diagnosis of BD3 are summarized in Table I.
机译：我们报道了一个符合Behçet病（BD）诊断标准并伴有脑出血的病例，该病例从这种脑血管并发症得到改善，并且在传统治疗后两年多的时间里一直没有BD的活动。作者认为这是一个风趣的报道，但草药可能对某些患有此病的患者有用。引言与当前过程相似的称为贝赫特氏病（BD），Adamantiades-贝赫特氏综合症，Halushi-贝赫克特氏综合症，眼-口腔-生殖器综合症，杜鹃碱性角化病或贝赫特氏三重症状复合体早在几个世纪前就被Hypocrates所描述，而并非偶然，在1937年由土耳其皮肤科医生Hulussi Beh？et对其进行了重新描述。大多数已确诊的患者已在古丝绸之路沿线找到，这些古丝绸之路从东亚延伸而来。根据流行病学，在2002年6月27日至29日于柏林举行的第十届国际贝希特氏病大会上发表的大多数论文都报告了在上述国家中BD的患病率较高[2]。流行病学调查结果表明，遗传因素和环境因素均会影响该疾病的发病机理。 BD是一种罕见的病因不明的慢性病，​​会影响年轻人的口腔和生殖器的内层以及包括眼睛和大脑在内的全身小血管，以及其他系统，导致复发的口腔和生殖器溃疡;那些溃疡可能发生在舌头，通常持续一到三周的嘴唇和脸颊内部，生殖器溃疡的出现频率要少于口腔溃疡，并且有时被误认为疱疹性病变;皮肤受累也很常见。可能会引起引起失明的葡萄膜炎和视网膜炎，以及关节炎，周围血管炎和神经系统并发症，通常被称为神经-贝氏综合征（NBS）。表I总结了诊断BD3的临床标准。

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