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两例血清抗伯氏疏螺旋体抗体升高的面瘫病例

[Two cases of facial diplegia with elevated serum antibodies to Borrelia burgdorferi].

作者信息

Matsumuro K, Izumo S, Nakamura A, Moritoyo T, Osame M

出版信息

Rinsho Shinkeigaku. 1989 Sep;29(9):1152-5.

PMID:2598542
Abstract

Lyme disease, a tick-borne infection with spirochete named Borrelia burgdorferi, is a complex multi-organ disorder involving neurological complication. Recently, the existence of Lyme disease was also recognized in middle Japan. We described here two cases of facial diplegia with elevated serum antibodies to B. burgdorferi. Case 1 was a 48 year-old man, who developed facial diplegia on April 29, 1987, and referred to our hospital on May 1. Neurological examination showed facial diplegia in addition to right-sided hemiparesis due to head injury of twenty years ago. The cell count of the cerebrospinal fluid was 17/mm3 and the protein was 139.9 mg/dl. The serological examinations for B. burgdorferi were performed by means of immunoperoxidase test. This patient had no serum IgG antibodies to B. burgdorferi on admission. However, twelve weeks later his serum showed significant elevation of IgG antibodies (titer: X400). Tests for syphilis and leptospira were negative. Based on these observation, we considered that facial diplegia of this patient was associated with the infection of B. burgdorferi. His facial diplegia remained unchanged with oral corticosteroid treatment. Case 2 was a 64 year-old man, who developed facial diplegia on May 31, 1987, and referred to our hospital on June 3. Neurological examinations were entirely negative except for facial diplegia. The findings of the cerebrospinal fluid showed the albumin cytologic dissociation with the cell count 2/mm3 and the protein 85.4 mg/dl. Serum IgG antibodies to B. burgdorferi were present (titer: X200) on admission. However, seven weeks later his serum showed a marked elevation of IgG antibodies (titer: X1600). Tests for syphilis were negative.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

莱姆病是一种由名为伯氏疏螺旋体的螺旋体通过蜱传播的感染性疾病,是一种涉及神经并发症的复杂多器官疾病。最近,日本中部地区也发现了莱姆病的存在。我们在此描述了两例血清中抗伯氏疏螺旋体抗体升高的双侧面瘫病例。病例1是一名48岁男性,于1987年4月29日出现双侧面瘫,并于5月1日转诊至我院。神经检查发现除因20年前头部受伤导致的右侧偏瘫外,还有双侧面瘫。脑脊液细胞计数为17/mm³,蛋白为139.9mg/dl。通过免疫过氧化物酶试验对伯氏疏螺旋体进行血清学检查。该患者入院时血清中没有抗伯氏疏螺旋体的IgG抗体。然而,12周后其血清中IgG抗体显著升高(滴度:X400)。梅毒和钩端螺旋体检测均为阴性。基于这些观察结果,我们认为该患者的双侧面瘫与伯氏疏螺旋体感染有关。口服皮质类固醇治疗后其双侧面瘫无变化。病例2是一名64岁男性,于1987年5月31日出现双侧面瘫,并于6月3日转诊至我院。除双侧面瘫外,神经检查完全正常。脑脊液检查结果显示蛋白细胞分离,细胞计数为2/mm³,蛋白为85.4mg/dl。入院时血清中存在抗伯氏疏螺旋体的IgG抗体(滴度:X200)。然而,7周后其血清中IgG抗体显著升高(滴度:X1600)。梅毒检测为阴性。(摘要截选至250字)

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